Skip Navigation
Skip to contents

J Pathol Transl Med : Journal of Pathology and Translational Medicine

OPEN ACCESS
SEARCH
Search

Search

Page Path
HOME > Search
116 "Adenoma"
Filter
Filter
Article category
Keywords
Publication year
Authors
Funded articles
Original Article
Article image
Adenomatoid odontogenic tumor: clinicopathological analysis of 34 cases from Karachi, Pakistan
Summaya Zafar, Sehar Sulaiman, Madeeha Nisar, Poonum Khan, Nasir Ud Din
J Pathol Transl Med. 2025;59(6):390-397.   Published online October 16, 2025
DOI: https://doi.org/10.4132/jptm.2025.07.11
  • 1,886 View
  • 135 Download
AbstractAbstract PDF
Background
Adenomatoid odontogenic tumor (AOT) is a benign slow-growing neoplasm of odontogenic epithelial origin that is relatively uncommon. Only a few studies have described its histological features. Hence, we aimed to describe the clinicopathological features of AOT in a cohort of patients. Methods: AOT cases diagnosed between 2009 and 2024 were searched electronically. Glass slides were retrieved from archives and were reviewed by two pathologists to record the associated morphological features. Other data including patient demographics and tumor site were collected by reviewing histopathology reports. Results: The age of patients ranged from 9 to 44 years (mean, 17.7 years), and most were female (55.9%). The maxilla (44.1%) was the most common tumor site. Histologically, a predominantly solid growth pattern (n = 34) accompanied by ducts with a cuboidal/columnar epithelial lining (n = 31), eosinophilic secretions (n = 31), calcifications (n = 31), lattice work pattern (n = 30), and cystic areas (n = 20) were observed. Less frequent features included calcifying epithelial odontogenic tumor (CEOT)–like areas (n = 13), osteodentin (n = 6), association with impacted tooth (n = 3), mucin in tubules (n = 7), fibrocollagenous stroma (n = 6), mucin in ducts (n = 3) and ossifying fibroma-like areas (n = 6). The association of ducts with a cuboidal/columnar epithelial lining, lattice work pattern, calcifications, and eosinophilic secretions with gingival tumors was statistically significant (p ≤ .05). Additionally, tooth tumors were significantly associated with CEOT-like areas (p = .03). Conclusions: Our study confirms the trends in the clinicopathological features of AOT in previous case reports. Our results suggest that AOTs usually exhibit a predominantly solid pattern with duct-like spaces. Only a few cases with CEOT-like and ossifying fibroma-like areas were observed, similar to infrequent cases reported in the past.
Case Study
Article image
Cytological features of atypical adenomatous hyperplasia and adenocarcinoma in situ of the lung: a case report
Misa Takahashi, Seiya Homma, Chisato Setoguchi, Yoko Umezawa, Atsuhiko Sakamoto
J Pathol Transl Med. 2025;59(3):195-200.   Published online May 9, 2025
DOI: https://doi.org/10.4132/jptm.2025.04.09
  • 3,990 View
  • 130 Download
AbstractAbstract PDF
Atypical adenomatous hyperplasia (AAH) and adenocarcinoma in situ (AIS) are generally treated as different lesions, depending on the differences in lesion size and histological findings. However, these differences are not absolute; thus, AAH and AIS are often difficult to distinguish. Moreover, whether AAH and AIS can be regarded as different lesions remains unknown because cytological specimens, especially those of AAH, are rare. In this study, we examined these uncommon cytological specimens and compared the cytological findings between AAH and AIS. We observed many common cytological features with no obvious differences between AAH and AIS. These findings suggest that these two distinct lesions can be grouped into a single category. Therefore, we propose creating a new cytological category.
Original Article
Article image
Fine needle aspiration cytology diagnoses of follicular thyroid carcinoma: results from a multicenter study in Asia
Hee Young Na, Miyoko Higuchi, Shinya Satoh, Kaori Kameyama, Chan Kwon Jung, Su-Jin Shin, Shipra Agarwal, Jen-Fan Hang, Yun Zhu, Zhiyan Liu, Andrey Bychkov, Kennichi Kakudo, So Yeon Park
J Pathol Transl Med. 2024;58(6):331-340.   Published online November 7, 2024
DOI: https://doi.org/10.4132/jptm.2024.10.12
  • 5,784 View
  • 266 Download
  • 1 Crossref
AbstractAbstract PDFSupplementary Material
Background
This study was designed to compare diagnostic categories of thyroid fine needle aspiration cytology (FNAC) and incidence of thyroid tumors in the multi-institutional Asian series with a special focus on diagnostic category IV (suspicious for a follicular neoplasm) and follicular thyroid carcinomas (FTCs). Methods: Distribution of FNAC categories, incidence of thyroid tumors in resection specimens and cytologic diagnoses of surgically confirmed follicular adenomas (FAs) and FTCs were collected from 10 institutes from five Asian countries and were compared among countries and between FAs and FTCs. Results: The frequency of category IV diagnoses (3.0%) in preoperative FNAC were significantly lower compared to those in Western countries (10.1%). When comparing diagnostic categories among Asian countries, category IV was more frequent in Japan (4.6%) and India (7.9%) than in Taiwan (1.4%), Korea (1.4%), and China (3.6%). Similarly, incidence of FAs and FTCs in surgical resection specimens was significantly higher in Japan (10.9%) and India (10.1%) than in Taiwan (5.5%), Korea (3.0%), and China (2.5%). FTCs were more commonly diagnosed as category IV in Japan (77.5%) than in Korea (33.3%) and China (35.0%). Nuclear pleomorphism, nuclear crowding, microfollicular pattern, and dyshesive cell pattern were more common in FTCs compared with FAs. Conclusions: Our study highlighted the difference in FNAC diagnostic categories of FTCs among Asian countries, which is likely related to different reporting systems and thyroid cancer incidence. Cytologic features such as nuclear pleomorphism, nuclear crowding, microfollicular pattern, and dyshesive cell pattern were found to be useful in diagnosing FTCs more effectively.

Citations

Citations to this article as recorded by  
  • Misdiagnosed follicular adenoma with 11 year postoperative liver and lung metastases a case report and literature review
    Kai-Li Yang, Heng-Tong Han, Shou-Hua Li, Xiao-Xiao Li, Ze Yang, Li-Bin Ma, Yong-Xun Zhao
    Discover Oncology.2025;[Epub]     CrossRef
Case Study
Article image
Tubular adenoma arising in tubular colonic duplication: a case report
Heonwoo Lee, Hyeong Rok An, Chan Wook Kim, Young Soo Park
J Pathol Transl Med. 2024;58(4):198-200.   Published online July 3, 2024
DOI: https://doi.org/10.4132/jptm.2024.06.04
  • 4,113 View
  • 220 Download
  • 1 Web of Science
  • 1 Crossref
AbstractAbstract PDF
Colonic duplication constitutes a rare congenital anomaly, characterized by the presence of hollow cystic or tubular structures exhibiting an epithelial-lined intestinal wall. Diagnostic challenges persist due to its low incidence and manifestation of nonspecific symptoms such as abdominal pain or constipation, resulting in a reluctance to pursue surgical resection. As associated malignancies in colonic duplication are rare, the inherent malignant potential of these anomalies remains undetermined. Additionally, despite reported instances of associated malignancies in colonic duplication, there is an absence of reports in the literature detailing tubular adenoma within these cases. The histologic features of the presented case are particularly noteworthy, situated at the precancerous stage, intimating potential progression towards adenocarcinoma within colonic duplication.

Citations

Citations to this article as recorded by  
  • Low-grade mucinous neoplasm originating from intestinal duplication: a case report and review of the literature
    Huihui Yin, Jie Yu, Yunzhao Chen
    World Journal of Surgical Oncology.2025;[Epub]     CrossRef
Original Articles
Article image
Frequent apocrine changes in pleomorphic adenoma with malignant transformation: a possible pre-malignant step in ductal carcinoma ex pleomorphic adenoma
Joon Seon Song, Yeseul Kim, Yoon-Se Lee, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Kyung-Ja Cho
J Pathol Transl Med. 2023;57(3):158-165.   Published online May 10, 2023
DOI: https://doi.org/10.4132/jptm.2023.03.13
  • 6,852 View
  • 192 Download
  • 3 Web of Science
  • 3 Crossref
AbstractAbstract PDF
Background
The most common type of carcinoma ex pleomorphic adenoma (CPA) is histologically equivalent to salivary duct carcinoma, which has an apocrine phenotype. Invasive CPA is often accompanied by non-invasive or in situ carcinoma, an observation that suggests the presence of precursor lesions. The aim of this study was to identify candidate precursor lesions of CPA within pleomorphic adenoma (PA).
Methods
Eleven resected cases of CPA with residual PA and 17 cases of PA with atypical changes were subjected to immunohistochemistry (IHC) for p53, human epidermal growth factor receptor 2 (HER2), androgen receptor (AR), pleomorphic adenoma gene 1, gross cystic disease fluid protein-15 (GCDFP-15), and anti-mitochondrial antibody.
Results
Invasive or in situ carcinoma cells in all CPAs were positive for AR, GCDFP-15, and HER2. Atypical foci in PAs corresponded to either apocrine or oncocytic changes on the basis of their reactivity to AR, GCDFP-15, and anti-mitochondrial antibody. Atypical cells in PAs surrounding CPAs had an apocrine phenotype without HER2 expression.
Conclusions
Our study identified frequent apocrine changes in residual PAs in CPA cases, suggesting a possible precursor role of apocrine changes. We recommend the use of HER2 IHC in atypical PAs, and that clinicians take HER2 positivity into serious consideration.

Citations

Citations to this article as recorded by  
  • Pleomorphic Adenoma with Epithelial Atypia, Apocrine Metaplasia, and/or In situ/Intracapsular Salivary Duct Carcinoma Are Indolent Lesions with Good Prognosis: A Proposal for Unified Nomenclature and Clinical Observation
    Grayson G. Cole, Matt Levin, David Ferber, Spencer C. Roark, Peter M. Sadow, Daniel Lubin, Julie Guilmette, Jason R. Pettus, Adam S. Fisch, Dipti P. Sajed, Fouad R. Zakka, Mark W. Lingen, Nicole A. Cipriani
    Head and Neck Pathology.2025;[Epub]     CrossRef
  • Progression of Nasopharyngeal Pleomorphic Adenoma to Carcinoma Ex Pleomorphic Adenoma With Metastases: A Case Report
    Krystsina Zhukovich, Alisher Tashbayev, Vladimir Osipov
    Cureus.2025;[Epub]     CrossRef
  • Characterization of a Molecularly Distinct Subset of Oncocytic Pleomorphic Adenomas/Myoepitheliomas Harboring Recurrent ZBTB47-AS1::PLAG1 Gene Fusion
    Ziyad Alsugair, Jimmy Perrot, Françoise Descotes, Jonathan Lopez, Anne Champagnac, Daniel Pissaloux, Claire Castain, Mihaela Onea, Philippe Céruse, Pierre Philouze, Charles Lépine, Marie-Delphine Lanic, Marick Laé, Valérie Costes-Martineau, Nazim Benzerdj
    American Journal of Surgical Pathology.2024; 48(5): 551.     CrossRef
Article image
Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas
Su Jung Kum, Hye Won Lee, Soon Gu Kim, Hyungsik Park, Ilseon Hwang, Sang Pyo Kim
J Pathol Transl Med. 2022;56(1):22-31.   Published online October 15, 2021
DOI: https://doi.org/10.4132/jptm.2021.08.31
  • 6,937 View
  • 212 Download
  • 7 Web of Science
  • 6 Crossref
AbstractAbstract PDF
Background
Pituitary tumor transforming gene 1 (PTTG1), paired-like homeodomain 2 (PITX2), and galectin-3 have been widely studied as predictive biomarkers for various tumors and are involved in tumorigenesis and tumor progression. We evaluated the usefulness of PTTG1, PITX2, and galectin-3 as predictive biomarkers for invasive non-functioning pituitary adenomas (NFPAs) by determining the relationship between the expressions of these three proteins and the invasiveness of the NFPAs. We also investigated whether PTTG1, E-cadherin, and Ki-67, which are known to be related to each other, show a correlation with NFPA features.
Methods
A retrospective study was conducted on 87 patients with NPFAs who underwent surgical removal. The NFPAs were classified into three groups based on magnetic resonance imaging findings of suprasellar extension and cavernous sinus invasion. Immunohistochemical staining for PTTG1, PITX2, galectin-3, E-cadherin, and Ki-67 was performed on tissue microarrays.
Results
PTTG1 expression showed a statistically significant correlation with the invasiveness of NFPAs, whereas PITX2 and galectin-3 did not have a relationship with the invasiveness of NFPAs. Moreover, there was no association among PTTG1, E-cadherin, and Ki-67 expression.
Conclusions
PTTG1 has the potential to serve as a predictive biomarker for invasive NFPA. Furthermore, this study may serve as a reference for the development of PTTG1-targeted therapeutic agents.

Citations

Citations to this article as recorded by  
  • The regulatory role of PTTG1 in proliferation and migration of thyroid cancer
    Jianjun Wang, Chenjun Guo, Junyu Cao, Li Li
    Discover Oncology.2025;[Epub]     CrossRef
  • Biomarkers Driving Precision Medicine in Nonfunctioning Pituitary Neuroendocrine Tumors: A Systematic Review of Recent Literature
    Amalina Haydar Ali Tajuddin, Nur Firdaus Isa, Mohd Hamzah Mohd Nasir
    The Journal of Clinical Endocrinology & Metabolism.2025;[Epub]     CrossRef
  • High-throughput Screening for Cushing Disease: Therapeutic Potential of Thiostrepton via Cell Cycle Regulation
    Takuro Hakata, Ichiro Yamauchi, Daisuke Kosugi, Taku Sugawa, Haruka Fujita, Kentaro Okamoto, Yohei Ueda, Toshihito Fujii, Daisuke Taura, Nobuya Inagaki
    Endocrinology.2024;[Epub]     CrossRef
  • Neoplasms and tumor-like lesions of the sellar region: imaging findings with correlation to pathology and 2021 WHO classification
    Lorenzo Ugga, Raduan Ahmed Franca, Alessandra Scaravilli, Domenico Solari, Sirio Cocozza, Fabio Tortora, Luigi Maria Cavallo, Marialaura Del Basso De Caro, Andrea Elefante
    Neuroradiology.2023; 65(4): 675.     CrossRef
  • A comprehensive characterisation of phaeochromocytoma and paraganglioma tumours through histone protein profiling, DNA methylation and transcriptomic analysis genome wide
    Prodromos Chatzikyriakou, Dimitria Brempou, Mark Quinn, Lauren Fishbein, Roberta Noberini, Ioannis N. Anastopoulos, Nicola Tufton, Eugenie S. Lim, Rupert Obholzer, Johnathan G. Hubbard, Mufaddal Moonim, Tiziana Bonaldi, Katherine L. Nathanson, Louise Izat
    Clinical Epigenetics.2023;[Epub]     CrossRef
  • Expression and clinical significance of Cathepsin K and MMPs in invasive non-functioning pituitary adenomas
    Hongyan Liu, Saichun Zhang, Ting Wu, Zhaohui Lv, Jianming Ba, Weijun Gu, Yiming Mu
    Frontiers in Oncology.2022;[Epub]     CrossRef
Reviews
Article image
Hepatocellular adenomas: recent updates
Haeryoung Kim, Young Nyun Park
J Pathol Transl Med. 2021;55(3):171-180.   Published online April 7, 2021
DOI: https://doi.org/10.4132/jptm.2021.02.27
  • 11,619 View
  • 547 Download
  • 8 Web of Science
  • 10 Crossref
AbstractAbstract PDF
Hepatocellular adenoma (HCA) is a heterogeneous entity, from both the histomorphological and molecular aspects, and the resultant subclassification has brought a strong translational impact for both pathologists and clinicians. In this review, we provide an overview of the recent updates on HCA from the pathologists’ perspective and discuss several practical issues and pitfalls that may be useful for diagnostic practice.

Citations

Citations to this article as recorded by  
  • Preventing false positive imaging diagnosis of HCC: differentiating HCC from mimickers and practical strategies
    Ijin Joo
    Journal of Liver Cancer.2025; 25(2): 217.     CrossRef
  • Prognostic role of selection criteria for liver transplantation in patients with hepatocellular carcinoma: Review and bibliometric
    Pamela Scarlett Espinoza Loyola, Diana Laura Muratalla Bautista, Karen Adela Hernández Bautista, Elizabeth Gil White, José Antonio González Moreno, Daniel Angel Torres del Real, Víctor Manuel Páez Zayas, Carla Escorza-Molina, Fernando Mondragón Rodríguez,
    iLIVER.2024; 3(1): 100077.     CrossRef
  • ACG Clinical Guideline: Focal Liver Lesions
    Catherine Frenette, Mishal Mendiratta-Lala, Reena Salgia, Robert J. Wong, Bryan G. Sauer, Anjana Pillai
    American Journal of Gastroenterology.2024; 119(7): 1235.     CrossRef
  • Hepatocellular adenoma update: diagnosis, molecular classification, and clinical course
    Sarah Poetter-Lang, Ahmed Ba-Ssalamah, Nina Bastati, Sami A Ba-Ssalamah, Jacqueline C Hodge, Giuseppe Brancatelli, Valérie Paradis, Valérie Vilgrain
    British Journal of Radiology.2024; 97(1163): 1740.     CrossRef
  • Fatal rupture of hepatic adenomatosis: Autopsy case and review of the literature
    Sarra Ben Abderrahim, Khouloud Chérif, Zeineb Nfikha, Sarra Gharsallaoui, Imen El Aini, Maher Jedidi, Moncef Mokni, Mohamed Ben Dhiab
    Journal of Forensic Sciences.2023; 68(4): 1393.     CrossRef
  • Large Hepatocellular Adenoma Presenting with Iron Deficiency Anemia: A Case Report
    Young Kwon Koh, Su Hyun Yoon, Sung Han Kang, Hyery Kim, Ho Joon Im, Suhyeon Ha, Jung-Man Namgoong, Kyung-Nam Koh
    Clinical Pediatric Hematology-Oncology.2023; 30(1): 25.     CrossRef
  • A Case Report on a Giant Hepatic Inflammatory Adenoma in a Young Female That Presented as Spontaneous Intrahepatic Hematoma
    Andreas Kyvetos, Panagiota Voukelatou, Ioannis Vrettos, Spyridon Pantzios , Ioannis Elefsiniotis
    Cureus.2023;[Epub]     CrossRef
  • Advances in Histological and Molecular Classification of Hepatocellular Carcinoma
    Joon Hyuk Choi, Swan N. Thung
    Biomedicines.2023; 11(9): 2582.     CrossRef
  • Estrobolome and Hepatocellular Adenomas—Connecting the Dots of the Gut Microbial β-Glucuronidase Pathway as a Metabolic Link
    Sandica Bucurica, Mihaela Lupanciuc, Florentina Ionita-Radu, Ion Stefan, Alice Elena Munteanu, Daniela Anghel, Mariana Jinga, Elena Laura Gaman
    International Journal of Molecular Sciences.2023; 24(22): 16034.     CrossRef
  • Hepatocellular adenoma: what we know, what we do not know, and why it matters
    Paulette Bioulac‐Sage, Annette S H Gouw, Charles Balabaud, Christine Sempoux
    Histopathology.2022; 80(6): 878.     CrossRef
Article image
Evolving pathologic concepts of serrated lesions of the colorectum
Jung Ho Kim, Gyeong Hoon Kang
J Pathol Transl Med. 2020;54(4):276-289.   Published online June 26, 2020
DOI: https://doi.org/10.4132/jptm.2020.04.15
  • 18,172 View
  • 842 Download
  • 36 Web of Science
  • 34 Crossref
AbstractAbstract PDFSupplementary Material
Here, we provide an up-to-date review of the histopathology and molecular pathology of serrated colorectal lesions. First, we introduce the updated contents of the 2019 World Health Organization classification for serrated lesions. The sessile serrated lesion (SSL) is a new diagnostic terminology that replaces sessile serrated adenoma and sessile serrated polyp. The diagnostic criteria for SSL were revised to require only one unequivocal distorted serrated crypt, which is sufficient for diagnosis. Unclassified serrated adenomas have been included as a new category of serrated lesions. Second, we review ongoing issues concerning the morphology of serrated lesions. Minor morphologic variants with distinct molecular features were recently defined, including serrated tubulovillous adenoma, mucin-rich variant of traditional serrated adenoma (TSA), and superficially serrated adenoma. In addition to intestinal dysplasia and serrated dysplasia, minimal deviation dysplasia and not otherwise specified dysplasia were newly suggested as dysplasia subtypes of SSLs. Third, we summarize the molecular features of serrated lesions. The critical determinant of CpG island methylation development in SSLs is patient age. Interestingly, there may be ethnic differences in BRAF/KRAS mutation frequencies in SSLs. The molecular pathogenesis of TSAs is divided into KRAS and BRAF mutation pathways. SSLs with MLH1 methylation can progress into favorable prognostic microsatellite instability-positive (MSI+)/CpG island methylator phenotype-positive (CIMP+) carcinomas, whereas MLH1-unmethylated SSLs and BRAF-mutated TSAs can be precursors of poor-prognostic MSI−/CIMP+ carcinomas. Finally, based on our recent data, we propose an algorithm for stratifying risk subgroups of non-dysplastic SSLs.

Citations

Citations to this article as recorded by  
  • Predominant Serrated Molecular Signature in Postcolonoscopy Colorectal Cancer: A Systematic Review and Meta-Analysis
    Jen-Hao Yeh, Sin-Hua Moi, Chia-Chi Chen, Chao-Wen Hsu, Wen-Shuo Yeh, Tzu-Ning Tseng, Chuan-Pin Lin, Yu-Peng Liu, Jaw-Yuan Wang
    American Journal of Gastroenterology.2026; 121(1): 122.     CrossRef
  • Clinical and endoscopic characteristics of colorectal traditional serrated adenomas with dysplasia/adenocarcinoma in a Korean population
    Ki-Hyun Kim, Eun Myung, Hyung Hoon Oh, Chan-Muk Im, Young-Eun Seo, Je-Seong Kim, Chae-June Lim, Ga-Ram You, Sung-Bum Cho, Wan-Sik Lee, Myung-Giun Noh, Kyung-Hwa Lee, Young-Eun Joo
    World Journal of Gastrointestinal Oncology.2025;[Epub]     CrossRef
  • MicroRNA: role in macrophage polarisation and colorectal cancer pathogenesis
    Haihong Lin, Jun Zhou, Ying He, Yifan Zhu, Puwen Chen, Hongwei Yan, Junyun Huang, Ersheng Gong, Xiaoling Wang
    Frontiers in Cell and Developmental Biology.2025;[Epub]     CrossRef
  • Submucosal fibrosis in large colorectal serrated lesions in cases receiving endoscopic submucosal dissection
    Erik Manriquez-Alegria, Naohisa Yoshida, Reo Kobayashi, Naoto Iwai, Ken Inoue, Osamu Dohi, Lucas Cardoso, Hideyuki Konishi
    Therapeutic Advances in Gastroenterology.2025;[Epub]     CrossRef
  • Navigating the Colorectal Cancer Maze: Unveiling Pathways To Diagnosis, Management, Pathophysiology and Prevention
    Khalid Ali Mohammed Al Kamzari, Constantina Constantinou
    Current Oncology Reports.2025; 27(10): 1115.     CrossRef
  • Fosl1 is a transcriptional effector of BRAFV600E-driven intestinal tumorigenesis
    Zakia Alam, Rebecca Nightingale, Analia Lesmana, Cheng Liu, Laura J. Jenkins, Mark F. Richardson, Lawrence Croft, Ian Y. Luk, Camilla M. Reehorst, Fiona Chionh, Natalia Vukelic, Faiza Basheer, Eugene Tulchinsky, Joshua Badshah, Troy Dumenil, Latifa Bakiri
    iScience.2025; 28(11): 113875.     CrossRef
  • Sessile Serrated Lesions in Inflammatory Bowel Disease: Hidden Players in Colitis-Associated Colorectal Cancer?
    Roberto de Sire, Diletta De Deo, Miriana Mercurio, Gianluca Franchellucci, Giulio Calabrese, Livio Bonacci, Mauro Sollai Pinna, Cristina Bezzio, Alessandro Armuzzi, Cesare Hassan, Alessandro Repici, Fabiana Castiglione, Sandro Ardizzone, Roberta Maselli
    Journal of Clinical Medicine.2025; 14(22): 8042.     CrossRef
  • Histologic Reappraisal and Evaluation of MLH1 Protein Expression in Sessile Serrated Lesions of the Proximal Colon
    Priscilla de Sene Portel Oliveira, Miriam Aparecida da Silva Trevisan, Rita Barbosa de Carvalho, Rita de Cássia Perina Martins, João José Fagundes, Claudio Saddy Rodrigues Coy, Ashwini Esnakula
    Gastroenterology Research and Practice.2025;[Epub]     CrossRef
  • Impact of AI-aided colonoscopy in clinical practice: a prospective randomised controlled trial
    Johanna Schöler, Marko Alavanja, Thomas de Lange, Shunsuke Yamamoto, Per Hedenström, Jonas Varkey
    BMJ Open Gastroenterology.2024; 11(1): e001247.     CrossRef
  • The histologic features, molecular features, detection and management of serrated polyps: a review
    Jin-Dong Wang, Guo-Shuai Xu, Xin-Long Hu, Wen-Qiang Li, Nan Yao, Fu-Zhou Han, Yin Zhang, Jun Qu
    Frontiers in Oncology.2024;[Epub]     CrossRef
  • Serrated polyps <10 mm cannot reliably be characterized by i-Scan without magnification at routine colonoscopy
    Sabrina G.G. TESTONI, Chiara NOTARISTEFANO, Giuliano F. BONURA, Maria NAPOLITANO, Dario ESPOSITO, Edi VIALE, Lorella FANTI, Francesco AZZOLINI, Giulia M. CAVESTRO, PierAlberto TESTONI
    Minerva Gastroenterology.2024;[Epub]     CrossRef
  • Interobserver variability in the histopathological classification and grading of dysplasia in elevated colon lesions in the city of Lima
    Guido Gallegos-Serruto, Aldo Gutiérrez, César Chian García, Isthvan Torres Perez
    Revista de Gastroenterología del Perú.2024; 44(3): 239.     CrossRef
  • Comparison of adenoma detection rate and proximal serrated polyp detection rate and their effect on post-colonoscopy colorectal cancer mortality in screening patients
    Jasmin Zessner-Spitzenberg, Elisabeth Waldmann, Lena Jiricka, Lisa-Maria Rockenbauer, Anna Hinterberger, Jeremy Cook, Arno Asaturi, Aleksandra Szymanska, Barbara Majcher, Michael Trauner, Monika Ferlitsch
    Endoscopy.2023; 55(05): 434.     CrossRef
  • The yield of dysplasia and serrated lesions in a single-centre tertiary inflammatory bowel disease cohort
    Fiona Yeaman, Lena Thin
    Therapeutic Advances in Gastroenterology.2023;[Epub]     CrossRef
  • The BEETS (JACCRO CC-18) Trial: An Observational and Translational Study of BRAF -Mutated Metastatic Colorectal Cancer
    Chiaki Inagaki, Ryo Matoba, Satoshi Yuki, Manabu Shiozawa, Akihito Tsuji, Eisuke Inoue, Kei Muro, Wataru Ichikawa, Masashi Fujii, Yu Sunakawa
    Future Oncology.2023; 19(17): 1165.     CrossRef
  • A retrospective analysis of the histology of resected polyps and colonoscopy quality parameters in Belgium
    E Macken, S Van Dongen, G Van Hal
    Acta Gastro Enterologica Belgica.2023; 86(2): 277.     CrossRef
  • Prognostic Biomarkers of Cell Proliferation in Colorectal Cancer (CRC): From Immunohistochemistry to Molecular Biology Techniques
    Aldona Kasprzak
    Cancers.2023; 15(18): 4570.     CrossRef
  • Assimilating Epigenetics and Transcriptomics for the Identification of Prognostic Novel Biomarkers and Imminent Targets in Colorectal Carcinoma with Therapeutic Potential
    Suman Kumar Ray, Sukhes Mukherjee
    Current Molecular Medicine.2023; 23(8): 784.     CrossRef
  • Multitarget Stool RNA Test for Colorectal Cancer Screening
    Erica K. Barnell, Elizabeth M. Wurtzler, Julie La Rocca, Thomas Fitzgerald, Jessica Petrone, Yansheng Hao, Yiming Kang, Faith L. Holmes, David A. Lieberman
    JAMA.2023; 330(18): 1760.     CrossRef
  • Microbiome in Colonic Carcinogenesis
    Jun Sun, Yinglin Xia
    Comprehensive Physiology.2023; 13(3): 4685.     CrossRef
  • Impact of comprehensive optical diagnosis training using Workgroup serrAted polypS and Polyposis classification on detection of adenoma and sessile serrated lesion
    Jooyoung Lee, Jung Ho Bae, Su Jin Chung, Hae Yeon Kang, Seung Joo Kang, Min‐Sun Kwak, Ji Yeon Seo, Ji Hyun Song, Sun Young Yang, Jong In Yang, Seon Hee Lim, Jeong Yoon Yim, Joo Hyun Lim, Goh Eun Chung, Eun Hyo Jin, Ji Min Choi, Yoo Min Han, Joo Sung Kim
    Digestive Endoscopy.2022; 34(1): 180.     CrossRef
  • Clinicopathological and molecular analyses of hyperplastic lesions including microvesicular variant and goblet cell rich variant hyperplastic polyps and hyperplastic nodules—Hyperplastic nodule is an independent histological entity
    Noriyuki Uesugi, Yoichi Ajioka, Tomio Arai, Yoshihito Tanaka, Tamotsu Sugai
    Pathology International.2022; 72(2): 128.     CrossRef
  • Comprehensive clinicopathologic, molecular, and immunologic characterization of colorectal carcinomas with loss of three intestinal markers, CDX2, SATB2, and KRT20
    Ji Ae Lee, Mi-Kyoung Seo, Seung-Yeon Yoo, Nam-Yun Cho, Yoonjin Kwak, Kyoungbun Lee, Jung Ho Kim, Gyeong Hoon Kang
    Virchows Archiv.2022; 480(3): 543.     CrossRef
  • Serrated Colorectal Lesions: An Up-to-Date Review from Histological Pattern to Molecular Pathogenesis
    Martino Mezzapesa, Giuseppe Losurdo, Francesca Celiberto, Salvatore Rizzi, Antonio d’Amati, Domenico Piscitelli, Enzo Ierardi, Alfredo Di Leo
    International Journal of Molecular Sciences.2022; 23(8): 4461.     CrossRef
  • Arterial stiffness is associated with high-risk colorectal adenomas and serrated lesions: A cross-sectional study in a Taiwanese population
    Hung-Yu Chen, Wen-Huang Lee, Hung-Lung Hsu, Yu-Tsung Chou, Fei-Lin Su, I-Hsuan Wu, Ting-Hsing Chao
    Journal of Cardiology.2022; 80(2): 139.     CrossRef
  • Morphological and molecular characterization of colorectal sessile serrated lesions with dysplasia
    Filippo Cappello, Valentina Angerilli, Luca Dal Santo, Giada Munari, Marianna Sabbadin, Marcello Lo Mele, Gianmaria Pennelli, Claudio Luchini, Paola Parente, Stefano Lazzi, Matteo Fassan
    Pathology - Research and Practice.2022; 240: 154214.     CrossRef
  • Serrated polyposis: an overview
    Jonathan Fawkes
    Gastrointestinal Nursing.2022; 20(9): 24.     CrossRef
  • Sessile serrated lesion presenting as large pedunculated polyp in the rectum: A case report
    Shin Ju Oh, Jung-Wook Kim, Chi Hyuk Oh
    Medicine.2022; 101(51): e32287.     CrossRef
  • WHICH LESIONS ARE AT HIGHER RISK OF DEVELOPING COLORECTAL CARCINOMAS: SUPERFICIALLY ELEVATED SERRATED LESIONS OR DEPRESSED LESIONS?
    Artur Adolfo PARADA, Filadelfio Euclydes VENCO, Miguel Reynaldo VARCA-NETO, Roberto EL IBRAHIM, Paula Bechara POLETTI, Helcio Pedrosa BRITO, Heloisa de Fátima SARE, Osvaldo MALAFAIA
    ABCD. Arquivos Brasileiros de Cirurgia Digestiva (São Paulo).2022;[Epub]     CrossRef
  • WNT5a in Colorectal Cancer: Research Progress and Challenges
    Guangshun Sun, Liangliang Wu, Guoqiang Sun, Xuesong Shi, Hongyong Cao, Weiwei Tang
    Cancer Management and Research.2021; Volume 13: 2483.     CrossRef
  • Endoscopic diagnosis for colorectal sessile serrated lesions
    Toshihiro Nishizawa, Shuntaro Yoshida, Akira Toyoshima, Tomoharu Yamada, Yoshiki Sakaguchi, Taiga Irako, Hirotoshi Ebinuma, Takanori Kanai, Kazuhiko Koike, Osamu Toyoshima
    World Journal of Gastroenterology.2021; 27(13): 1321.     CrossRef
  • NTRK oncogenic fusions are exclusively associated with the serrated neoplasia pathway in the colorectum and begin to occur in sessile serrated lesions
    Jung Ho Kim, Jeong Hoon Hong, Yoon‐La Choi, Ji Ae Lee, Mi‐kyoung Seo, Mi‐Sook Lee, Sung Bin An, Min Jung Sung, Nam‐Yun Cho, Sung‐Su Kim, Young Kee Shin, Sangwoo Kim, Gyeong Hoon Kang
    The Journal of Pathology.2021; 255(4): 399.     CrossRef
  • Differential pre-malignant programs and microenvironment chart distinct paths to malignancy in human colorectal polyps
    Bob Chen, Cherie’ R. Scurrah, Eliot T. McKinley, Alan J. Simmons, Marisol A. Ramirez-Solano, Xiangzhu Zhu, Nicholas O. Markham, Cody N. Heiser, Paige N. Vega, Andrea Rolong, Hyeyon Kim, Quanhu Sheng, Julia L. Drewes, Yuan Zhou, Austin N. Southard-Smith, Y
    Cell.2021; 184(26): 6262.     CrossRef
  • Molecular Insights Into Colorectal Carcinoma
    Domenika Ortiz Requena, Monica Garcia-Buitrago
    Archives of Medical Research.2020; 51(8): 839.     CrossRef
Original Articles
Article image
Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
Yo Han Jeon, Ji Hyun Ahn, Hee Kyung Chang
J Pathol Transl Med. 2020;54(2):135-145.   Published online January 29, 2020
DOI: https://doi.org/10.4132/jptm.2019.11.06
  • 9,730 View
  • 255 Download
  • 2 Web of Science
  • 2 Crossref
AbstractAbstract PDF
Background
Colorectal epithelial neoplasm extending into the submucosal gut-associated lymphoid tissue (GALT) can cause difficulties in the differential diagnosis. Regarding GALT-associated epithelial neoplasms, a few studies favor the term “GALT carcinoma” while other studies have mentioned the term “GALT-associated pseudoinvasion/epithelial misplacement (PEM)”.
Methods
The clinicopathologic characteristics of 11 cases of colorectal epithelial neoplasm associated with submucosal GALT diagnosed via endoscopic submucosal dissection were studied.
Results
Eight cases (72.7%) were in males. The median age was 59 years, and age ranged from 53 to 73. All cases had a submucosal tumor component more compatible with GALT-associated PEM. Eight cases (72.7%) were located in the right colon. Ten cases (90.9%) had a non-protruding endoscopic appearance. Nine cases (81.8%) showed continuity between the submucosal and surface adenomatous components. Nine cases showed (81.8%) focal defects or discontinuation of the muscularis mucosae adjacent to the submucosal GALT. No case showed hemosiderin deposits in the submucosa or desmoplastic reaction. No case showed single tumor cells or small clusters of tumor cells in the submucosal GALT. Seven cases (63.6%) showed goblet cells in the submucosa. No cases showed oncocytic columnar cells lining submucosal glands.
Conclusions
Our experience suggests that pathologists should be aware of the differential diagnosis of GALT-associated submucosal extension by colorectal adenomatous neoplasm. Further studies are needed to validate classification of GALT-associated epithelial neoplasms.

Citations

Citations to this article as recorded by  
  • Family adenomatous polyposis come across dome type adenocarcinoma: a case report and literature review
    Ying-Ying Chang, Xiao-Long Zhang, Yao-Hui Wang, Ting-Sheng Ling
    Diagnostic Pathology.2025;[Epub]     CrossRef
  • Radiation-induced injury and the gut microbiota: insights from a microbial perspective
    Qiaoli Wang, Guoqiang Xu, Ouying Yan, Shang Wang, Xin Wang
    Therapeutic Advances in Gastroenterology.2025;[Epub]     CrossRef
PLAG1, SOX10, and Myb Expression in Benign and Malignant Salivary Gland Neoplasms
Ji Hyun Lee, Hye Ju Kang, Chong Woo Yoo, Weon Seo Park, Jun Sun Ryu, Yuh-Seog Jung, Sung Weon Choi, Joo Yong Park, Nayoung Han
J Pathol Transl Med. 2019;53(1):23-30.   Published online November 14, 2018
DOI: https://doi.org/10.4132/jptm.2018.10.12
  • 12,652 View
  • 382 Download
  • 27 Web of Science
  • 34 Crossref
AbstractAbstract PDF
Background
Recent findings in molecular pathology suggest that genetic translocation and/oroverexpression of oncoproteins is important in salivary gland tumorigenesis and diagnosis. Weinvestigated PLAG1, SOX10, and Myb protein expression in various salivary gland neoplasm tissues.
Methods
A total of 113 cases of surgically resected salivary gland neoplasms at the NationalCancer Center from January 2007 to March 2017 were identified. Immunohistochemical stainingof PLAG1, SOX10, and Myb in tissue samples was performed using tissue microarrays.
Results
Among the 113 cases, 82 (72.6%) were benign and 31 (27.4%) were malignant. PLAG1 showednuclear staining and normal parotid gland was not stained. Among 48 cases of pleomorphicadenoma, 29 (60.4%) were positive for PLAG1. All other benign and malignant salivary glandneoplasms were PLAG1-negative. SOX10 showed nuclear staining. In normal salivary gland tissuesSOX10 was expressed in cells of acinus and intercalated ducts. In benign tumors, SOX10 expressionwas observed in all pleomorphic adenoma (48/48), and basal cell adenoma (3/3), but not inother benign tumors. SOX10 positivity was observed in nine of 31 (29.0%) malignant tumors.Myb showed nuclear staining but was not detected in normal parotid glands. Four of 31 (12.9%)malignant tumors showed Myb positivity: three adenoid cystic carcinomas (AdCC) and onemyoepithelial carcinoma with focal AdCC-like histology.
Conclusions
PLAG1 expression is specificto pleomorphic adenoma. SOX10 expression is helpful to rule out excretory duct origin tumor,but its diagnostic value is relatively low. Myb is useful for diagnosing AdCC when histology isunclear in the surgical specimen.

Citations

Citations to this article as recorded by  
  • PLEOMORPHIC ADENOMA: A COMPREHENSIVE REVIEW
    Wilson Duplessis, Jason K. Wasserman
    Seminars in Diagnostic Pathology.2026; : 150991.     CrossRef
  • Pleomorphic adenoma gene 1 (PLAG1) protects p53-/- myoepithelial cells from mitochondria-related apoptosis caused by hypoxia
    Nodoka Kindaichi, Yoshiki Mukudai, Yuzo Abe, Masataka Watanabe, Maki Nara, Konomi Yamada, Asami Houri, Toshikazu Shimane, Tatsuo Shirota
    Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2025; 37(4): 654.     CrossRef
  • Retrospective Clinicopathological Study of 33 Cases of Pleomorphic Salivary Adenoma Diagnosed in Benghazi
    Siraj S. Najem, Elhoni Ashour, Rehab Elmaddani, Ali M. Elmurtadi
    Libyan Journal of Dentistry .2025; 8(2): 29.     CrossRef
  • Pleomorphic adenoma of palatal minor salivary glands
    Afrah Aldelaimi, Tahrir Aldelaimi, Suzan Abdulkareem
    Revista Española de Cirugía Oral y Maxilofacial.2025;[Epub]     CrossRef
  • Immunohistochemical Characterization of a Large Cohort of Triple Negative Breast Cancer
    Rachel Han, Sharon Nofech-Mozes, Dina Boles, Hannah Wu, Nikolina Curcin, Elzbieta Slodkowska
    International Journal of Surgical Pathology.2024; 32(2): 239.     CrossRef
  • Proceedings of the 2024 North American Society of Head and Neck Pathology Companion Meeting, Baltimore, MD, March 24, 2024: Navigating Ancillary Studies in Basaloid/Blue Salivary Tumors
    Kristine S. Wong
    Head and Neck Pathology.2024;[Epub]     CrossRef
  • Insights into the molecular alterations of PLAG1 and HMGA2 associated with malignant phenotype acquisition in pleomorphic adenoma
    Reydson Alcides de Lima-Souza, Gustavo de Souza Vieira, Talita de Carvalho Kimura, João Figueira Scarini, Luccas Lavareze, Tayná Figueiredo Maciel, Moisés Willian Aparecido Gonçalves, Erika Said Abu Egal, Albina Altemani, Fernanda Viviane Mariano
    Critical Reviews in Oncology/Hematology.2024; 204: 104494.     CrossRef
  • Expanding the Molecular Spectrum of Carcinoma Ex Pleomorphic Adenoma
    Reydson Alcides de Lima-Souza, Albina Altemani, Michal Michal, Fernanda Viviane Mariano, Ilmo Leivo, Alena Skálová
    American Journal of Surgical Pathology.2024; 48(12): 1491.     CrossRef
  • Utility of SOX10 and estrogen receptor immunohistochemical expression in endometrial carcinoma of Egyptian patients
    Mona A. Kora, Alyaa A. Moselhy, Rania A. Abdallah
    Egyptian Journal of Pathology.2024; 44(2): 190.     CrossRef
  • Exploring Advanced Diagnostic Techniques for Salivary Gland Disorders: A Narrative Overview
    Chuan-Xiang Li-, Liu Zhang, Ya-Ru Yan, Yong-Jie Ding, Ying-Ni Lin, Jian-Ping Zhou, Ning Li, Hong-Peng Li, Shi-Qi Li, Xian-Wen Sun, Qing-Yun Li
    Asian journal of Current Research in Clinical Cancer.2024; 4(1): 1.     CrossRef
  • The Challenge of “Monomorphic” Mucoepidermoid Carcinoma—Report of a Rare Case with Pure Spindle-Clear Cell Morphology
    Xinyi Qu, Edwin Jun Chen Chew, Sathiyamoorthy Selvarajan, Bingcheng Wu, Abbas Agaimy, Fredrik Petersson
    Head and Neck Pathology.2023; 17(3): 864.     CrossRef
  • SOX10
    Albert L Sy, Mai P Hoang
    Journal of Clinical Pathology.2023; 76(10): 649.     CrossRef
  • Activating Transcription Factor 1 (ATF1) Immunohistochemical Marker Distinguishes HCCC from MEC
    Wafaey Badawy, Asmaa S. Abdelfattah, Haneen A. Sallam
    Journal of Molecular Pathology.2023; 4(3): 178.     CrossRef
  • Rare case of pleomorphic adenoma presenting as peritonsilar tumor
    Anđelina Jovanović, Svetlana Valjarević, Milan Jovanović
    Medicinska istrazivanja.2023; 56(3): 95.     CrossRef
  • Pleomorphic Adenoma of a Minor Salivary Gland of the Hard Palate: A Case Report
    Ishank Panchal, Anil Wanjari
    Cureus.2023;[Epub]     CrossRef
  • Advanced Diagnostic Methods for Salivary Glands Diseases: A Narrative Review Study
    Malak Mohammed AlOsaimi, Abdulaziz Mohammed AlSubaheen, Taif Saleh Jameel, Rand Abdulrahman AlSalamah, Dalal Naseh AlAnzi, Norah Ameen AlOushan, Fahad Fadhel AlShammari, Cristalle Soman
    Clinical Cancer Investigation Journal.2023; 12(4): 19.     CrossRef
  • Clinical Significance of SOX10 Expression in Human Pathology
    Hisham F. Bahmad, Aran Thiravialingam, Karthik Sriganeshan, Jeffrey Gonzalez, Veronica Alvarez, Stephanie Ocejo, Alvaro R. Abreu, Rima Avellan, Alejandro H. Arzola, Sana Hachem, Robert Poppiti
    Current Issues in Molecular Biology.2023; 45(12): 10131.     CrossRef
  • NR4A3 Immunostain Is a Highly Sensitive and Specific Marker for Acinic Cell Carcinoma in Cytologic and Surgical Specimens
    Kartik Viswanathan, Shaham Beg, Bing He, Taotao Zhang, Richard Cantley, Daniel J Lubin, Qiuying Shi, Zahra Maleki, Saeed Asiry, Rema Rao, Nora Katabi, Masato Nakaguro, William C Faquin, Peter M Sadow, Momin T Siddiqui, Theresa Scognamiglio
    American Journal of Clinical Pathology.2022; 157(1): 98.     CrossRef
  • Recent Advances on Immunohistochemistry and Molecular Biology for the Diagnosis of Adnexal Sweat Gland Tumors
    Nicolas Macagno, Pierre Sohier, Thibault Kervarrec, Daniel Pissaloux, Marie-Laure Jullie, Bernard Cribier, Maxime Battistella
    Cancers.2022; 14(3): 476.     CrossRef
  • Diagnostic accuracy of human transcriptional activator (Myb) expression by ELISA technique versus immunohistochemistry in detecting salivary gland carcinomas
    Yousra Refaey, OlfatGamil Shaker, Ayman Abdelwahab, ImanAdel Mohamed Abdelmoneim, Fat’heyaMohamed Zahran
    Journal of International Oral Health.2022; 14(1): 61.     CrossRef
  • SLUG is a key regulator of epithelial-mesenchymal transition in pleomorphic adenoma
    Hyesung Kim, Seung Bum Lee, Jae Kyung Myung, Jeong Hwan Park, Eunsun Park, Dong Il Kim, Cheol Lee, Younghoon Kim, Chul-Min Park, Min Bum Kim, Gil Chai Lim, Bogun Jang
    Laboratory Investigation.2022; 102(6): 631.     CrossRef
  • Assessment of MEF2C as a novel myoepithelial marker using normal salivary gland and pleomorphic adenoma: An immunohistochemical study
    Ikuko Takakura, Satoko Kujiraoka, Rika Yasuhara, Junichi Tanaka, Fumio Ide, Kenji Mishima
    Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2022; 34(4): 523.     CrossRef
  • Update on selective special types of breast neoplasms: Focusing on controversies, differential diagnosis, and molecular genetic advances
    Shi Wei
    Seminars in Diagnostic Pathology.2022; 39(5): 367.     CrossRef
  • Cutaneous Melanomas: A Single Center Experience on the Usage of Immunohistochemistry Applied for the Diagnosis
    Costantino Ricci, Emi Dika, Francesca Ambrosi, Martina Lambertini, Giulia Veronesi, Corti Barbara
    International Journal of Molecular Sciences.2022; 23(11): 5911.     CrossRef
  • Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
    Juan Ji, Fang Zhang, Fanglei Duan, Hong Yang, Jun Hou, Yang Liu, Jie Dai, Qiong Liao, Xian Chen, Qingsong Liu
    Scientific Reports.2022;[Epub]     CrossRef
  • NR4A3 fluorescence in situ hybridization analysis in cytologic and surgical specimens of acinic cell carcinoma
    Qiuying Shi, Bin Zhang, Caroline Bsirini, Liqiong Li, Ellen J. Giampoli, Kelly R. Magliocca, Michelle Reid, Zhongren Zhou
    Human Pathology.2022; 127: 86.     CrossRef
  • Evaluation of NR4A3 immunohistochemistry (IHC) and fluorescence in situ hybridization and comparison with DOG1 IHC for FNA diagnosis of acinic cell carcinoma
    John M. Skaugen, Raja R. Seethala, Simion I. Chiosea, Michael S. Landau
    Cancer Cytopathology.2021; 129(2): 104.     CrossRef
  • MYB-NFIB Translocation by FISH in Adenoid Cystic Carcinoma of the Head and Neck in Nigerian Patients: A Preliminary Report
    Adepitan A. Owosho, Olufunlola M. Adesina, Oluwole Odujoko, Olujide O. Soyele, Akinwumi Komolafe, Robert Bauer, Kallie Holte, Kurt F. Summersgill
    Head and Neck Pathology.2021; 15(2): 433.     CrossRef
  • Liquid-based cytology of oral brushings in a case of adenoid cystic carcinoma arising from the palate
    Ryo MAKINO, Akihiko KAWAHARA, Hideyuki ABE, Yorihiko TAKASE, Chihiro FUKUMITSU, Kazuya MURATA, Tomoko YOSHIDA, Yukako SHINODA, Yoshiki NAITO, Jun AKIBA
    The Journal of the Japanese Society of Clinical Cytology.2021; 60(1): 33.     CrossRef
  • MYB Translocations in Both Myoepithelial and Ductoglandular Epithelial Cells in Adenoid Cystic Carcinoma: A Histopathologic and Genetic Reappraisal in Six Primary Cutaneous Cases
    Keisuke Goto, Kazuyoshi Kajimoto, Takashi Sugino, Shin-ichi Nakatsuka, Makoto Yoshida, Mai Noto, Michihiro Kono, Toshihiro Takai
    The American Journal of Dermatopathology.2021; 43(4): 278.     CrossRef
  • Co-expression of Myoepithelial and Melanocytic Features in Carcinoma Ex Pleomorphic Adenoma
    Costantino Ricci, Federico Chiarucci, Francesca Ambrosi, Tiziana Balbi, Barbara Corti, Ottavio Piccin, Ernesto Pasquini, Maria Pia Foschini
    Head and Neck Pathology.2021; 15(4): 1385.     CrossRef
  • Juvenile onset pleomorphic adenoma presenting as giant tumor of parotid gland in a young female
    Surender Verma, Shivika Aggarwal, Pradeep Garg, Anjali Verma, Mridul Gera, Swaran S. Yadav
    Journal of Dr. NTR University of Health Sciences.2021; 10(4): 286.     CrossRef
  • Cytopathology and diagnostics of Warthin's tumour
    Mirna Sučić, Nives Ljubić, Leila Perković, Dunja Ivanović, Leo Pažanin, Tena Sučić Radovanović, Dubravka Župnić‐Krmek, Fabijan Knežević
    Cytopathology.2020; 31(3): 193.     CrossRef
  • Clear cell papillary neoplasm of the breast with MAML2 gene rearrangement: Clear cell hidradenoma or low-grade mucoepidermoid carcinoma?
    Raima A. Memon, Carlos N Prieto Granada, Shi Wei
    Pathology - Research and Practice.2020; 216(10): 153140.     CrossRef
Case Studies
Squamous Metaplasia in Pleomorphic Adenoma: A Diagnostic and Prognostic Enigma
Swati Sharma, Monica Mehendiratta, Nivedita Chaudhary, Vineet Gupta, Maulshree Kohli, Anjana Arora
J Pathol Transl Med. 2018;52(6):411-415.   Published online October 1, 2018
DOI: https://doi.org/10.4132/jptm.2018.07.15
  • 9,407 View
  • 144 Download
  • 11 Web of Science
  • 19 Crossref
AbstractAbstract PDF
Pleomorphic adenoma (PA) is the most common benign salivary gland tumor. Histologically, squamous metaplasia has been reported in PA, but has rarely been documented as being extensive enough to cause significant misdiagnosis. Here, we present an unusual case of PA in a 50-year-old female patient presenting with swelling on the postero-lateral aspect of the palate for a week. Histopathologically, the tumor exhibited the features of conventional PA with extensive squamous metaplasia and giant keratotic lamellae in cyst-like areas. Such exuberant squamous metaplasia and keratin can be a diagnostic and prognostic pitfall and lead to overtreatment of the patient.

Citations

Citations to this article as recorded by  
  • Retrospective Clinicopathological Study of 33 Cases of Pleomorphic Salivary Adenoma Diagnosed in Benghazi
    Siraj S. Najem, Elhoni Ashour, Rehab Elmaddani, Ali M. Elmurtadi
    Libyan Journal of Dentistry .2025; 8(2): 29.     CrossRef
  • Fine‐Needle Aspiration Cytology Diagnosis of Pleomorphic Adenoma With Spontaneous Infarction in the Salivary Gland: A Multicenter Retrospective Study
    Jie‐Qiong Wang, Ge Li, Shao‐Hua Wang, Bo Yang, Yun Liu, Yu Wan, Cong‐Gai Huang, Fan Li
    Cytopathology.2025; 36(5): 484.     CrossRef
  • Keratocystoma: Molecular insights and diagnostic challenges in a rare salivary gland tumor
    Yoshitaka Utsumi, Masato Nakaguro, Justin A. Bishop, Toshitaka Nagao
    Seminars in Diagnostic Pathology.2025; 42(5): 150940.     CrossRef
  • Bronchial pleomorphic adenoma successfully diagnosed and resected with left lower sleeve lobectomy; a case report and literature review
    Katsuhiro Itogawa, Tomohiro Oba, Mitsuru Maki, Masako Amano, Akiko Adachi, Hidekazu Matsushima
    Respiratory Medicine Case Reports.2025; 57: 102253.     CrossRef
  • Effective Management of a Giant Deforming Pleomorphic Adenoma With Airway Displacement in a 93-Year-Old Patient: A Case Report
    Julio A Palomino-Payan, Jessica Guillen-Valles, Daniel A Meza-Martinez, Fernanda Urias, Luis D Montes de Oca-Gordoa
    Cureus.2024;[Epub]     CrossRef
  • ECTOPIC PLEOMORPHIC ADENOMA OF BUCCAL SPACE: CASE REPORT WITH REVIEW OF LITERATURE
    SANCHIT BAJPAI
    UP STATE JOURNAL OF OTOLARYNGOLOGY AND HEAD AND NECK SURGERY.2024; VOLUME 12(ISSUE 1): 55.     CrossRef
  • Pleomorphic adenoma with extensive squamous metaplasia and keratinizing cysts: Diagnostic and clinical pitfalls – A report of two cases and review of literature
    Mahadevi B. Hosur, Rudrayya S. Puranik, Satyajit G. Dandagi, Vivekanand M. Patil
    Journal of Oral and Maxillofacial Pathology.2024; 28(4): 689.     CrossRef
  • Pleomorphic adenoma of the upper lip: A rare site for a common tumor- Case report
    Prasath Sathiah, Sujaya Mazumder, Santosh Tummidi, Vijay Kannaujiya
    SN Comprehensive Clinical Medicine.2023;[Epub]     CrossRef
  • Variable metaplastic entities in pleomorphic adenoma a review of a rare case report with a note on its significance
    N. Mahapatra, L. Bhuyan, Dash Chandra, P. Mishra
    Archive of Oncology.2023; 29(2): 18.     CrossRef
  • Pleomorphic adenoma with extensive oncocytic papillary cystic areas and trichilemmal keratinisation – A unique presentation
    CV Aiswarya, Raghunath Vandana, Kamal Firoz, Meda Samatha
    Journal of Oral and Maxillofacial Pathology.2023; 27(3): 562.     CrossRef
  • Pleomorphic Adenoma with Extensive Squamous and Adipocytic Metaplasia Mimicking as Low Grade Mucoepidermoid Carcinoma on FNAC
    Anu Singh, Ravi Hari Phulware, Arvind Ahuja, Ankur Gupta, Manju Kaushal
    Indian Journal of Otolaryngology and Head & Neck Surgery.2022; 74(S2): 2132.     CrossRef
  • Aspiration cytology of pleomorphic adenoma with squamous metaplasia: A case series and literature review illustrating diagnostic challenges
    Joshua J. X. Li, Joanna K. M. Ng, Eric H. L. Lau, Amy B. W. Chan
    Diagnostic Cytopathology.2022; 50(2): 64.     CrossRef
  • Pleomorphic adenoma with extensive squamous metaplasia: The first well-documented case involving the submandibular gland
    David A. Gaskin, Alain Reid, Pamela S. Gaskin
    Human Pathology Reports.2022; 27: 300600.     CrossRef
  • Salivary Gland Pleomorphic Adenomas Presenting With Extremely Varied Clinical Courses. A Single Institution Case-Control Study†
    Krzysztof Piwowarczyk, Ewelina Bartkowiak, Paweł Kosikowski, Jadzia Tin-Tsen Chou, Małgorzata Wierzbicka
    Frontiers in Oncology.2021;[Epub]     CrossRef
  • A case report of pleomorphic adenoma squamous metaplasia resembling metastatic oral squamous cell carcinoma
    E. Donohoe, R. Courtney, S. Phelan, P.J. McCann
    Advances in Oral and Maxillofacial Surgery.2021; 2: 100074.     CrossRef
  • Extensive squamous metaplasia in minor salivary gland neoplasm mimicking squamous cell carcinoma: Diagnostic dilemma in aspiration cytology
    Renu Sukumaran, Nileena Nayak, RariP Mony
    Clinical Cancer Investigation Journal.2021; 10(5): 257.     CrossRef
  • Navigating small biopsies of salivary gland tumors: a pattern-based approach
    J. Stephen Nix, Lisa M. Rooper
    Journal of the American Society of Cytopathology.2020; 9(5): 369.     CrossRef
  • Giant Parotid Pleomorphic Adenoma with Atypical Histological Presentation and Long‐Term Recurrence‐Free Follow‐Up after Surgery: A Case Report and Review of the Literature
    Mohammed AlKindi, Sundar Ramalingam, Lujain Abdulmajeed Hakeem, Manal A. AlSheddi, Pravinkumar G. Patil
    Case Reports in Dentistry.2020;[Epub]     CrossRef
  • Pleomorphic adenoma of soft palate with extensive squamous metaplasia – A diagnostic enigma
    Rashmi Patnayak, Sandip Mohanty, Anjan Kumar Sahoo, Adya Kinkara Panda, Amitabh Jena
    Journal of Dr. NTR University of Health Sciences.2019; 8(4): 268.     CrossRef
Hepatocellular Carcinoma Arising in a Huge Hepatocellular Adenoma with Bone Marrow Metaplasia
Hyo Jeong Kang, Hui Jeong Jeong, So-Woon Kim, Eunsil Yu, Young-Joo Lee, So Yeon Kim, Jihun Kim
J Pathol Transl Med. 2018;52(4):226-231.   Published online December 27, 2017
DOI: https://doi.org/10.4132/jptm.2017.11.12
  • 8,703 View
  • 152 Download
  • 5 Web of Science
  • 6 Crossref
AbstractAbstract PDF
Hepatocellular adenoma (HCA) is the most common type of benign liver tumor, and its major complication is malignant transformation to hepatocellular carcinoma (HCC). Here, we report a case of HCC arising in HCA with bone marrow metaplasia in a 24-year-old Korean woman who presented with abdominal discomfort. A huge liver mass was found on abdominal ultrasonography. She underwent surgical hepatic resection, and the resected specimen was entirely involved by a 20-cm-sized tumor. Histological review revealed a well differentiated HCC arising from inflammatory HCA with β-catenin nuclear positivity and bone marrow metaplasia that contained hematopoietic cells. This case was unique because malignant transformation, inflammatory type HCA, β-catenin nuclear staining, and bone marrow metaplasia were simultaneously observed. Additionally, it should be noted that a large HCA with β-catenin activation can undergo malignant transformation and should be surgically resected in a timely manner.

Citations

Citations to this article as recorded by  
  • Adult Hepatocellular Carcinoma Coexisting with Extramedullary Hematopoiesis
    Hirotsugu Noguchi, Michiyo Higashi, Ryo Desaki, Takashi Tasaki, Mari Kirishima, Ikumi Kitazono, Kazuhiro Tabata, Akihide Tanimoto
    International Journal of Surgical Pathology.2022; 30(3): 339.     CrossRef
  • Spontaneous Occurrence of Various Types of Hepatocellular Adenoma in the Livers of Metabolic Syndrome-Associated Steatohepatitis Model TSOD Mice
    Wenhua Shao, Orgil Jargalsaikhan, Mayuko Ichimura-Shimizu, Qinyi Cai, Hirohisa Ogawa, Yuko Miyakami, Kengo Atsumi, Mitsuru Tomita, Mitsuko Sutoh, Shunji Toyohara, Ryoji Hokao, Yasusei Kudo, Takeshi Oya, Koichi Tsuneyama
    International Journal of Molecular Sciences.2022; 23(19): 11923.     CrossRef
  • Bilateral Diffuse Nodular Pulmonary Ossification Mimicking Metastatic Disease in a Patient with Fibrolamellar Hepatocellular Carcinoma
    Pattamon Sutthatarn, Cara E. Morin, Jessica Gartrell, Wayne L. Furman, Max R. Langham, Teresa Santiago, Andrew J. Murphy
    Children.2021; 8(3): 226.     CrossRef
  • Malignant transformation of liver fatty acid binding protein-deficient hepatocellular adenomas: histopathologic spectrum of a rare phenomenon
    Juan Putra, Linda D. Ferrell, Annette S.H. Gouw, Valerie Paradis, Arvind Rishi, Christine Sempoux, Charles Balabaud, Swan N. Thung, Paulette Bioulac-Sage
    Modern Pathology.2020; 33(4): 665.     CrossRef
  • Hepatocellular carcinoma arising from hepatic adenoma in a young woman
    Haythem Yacoub, Hela Kchir, Dhouha Cherif, Hajer Hassine, Slim Haouet, Asma Ayari, Habiba Mizouni, Saber Mannai, Mohamed Tahar Khalfallah, Nadia Maamouri
    Clinical Case Reports.2020; 8(9): 1659.     CrossRef
  • Metanephric adenoma with osseous metaplasia and bone marrow elements
    Alessandro Pietro Aldera, Jeff John, Dharshnee Chetty, Dhirendra Govender
    Human Pathology: Case Reports.2019; 17: 200316.     CrossRef
Mucinous Cystadenoma of the Testis: A Case Report with Immunohistochemical Findings
Gilhyang Kim, Dohee Kwon, Hee Young Na, Sehui Kim, Kyung Chul Moon
J Pathol Transl Med. 2017;51(2):180-184.   Published online February 13, 2017
DOI: https://doi.org/10.4132/jptm.2016.08.30
  • 10,626 View
  • 126 Download
  • 5 Web of Science
  • 8 Crossref
AbstractAbstract PDF
Mucinous cystadenoma of the testis is a very rare tumor. Herein, we report a case of mucinous cystadenoma arising in the testis of a 61-year-old man, along with a literature review. Computed tomography showed a 2.5-cm-sized poorly enhancing cystic mass. Grossly, the tumor was a unilocular cystic mass filled with mucinous material and confined to the testicular parenchyma. Histologically, the cyst had a fibrotic wall lined by mucinous columnar epithelium without atypia. Immunohistochemical staining was positive for cytokeratin 20 and CDX2, as well as focally positive for cytokeratin 7. The pathologic diagnosis was mucinous cystadenoma.

Citations

Citations to this article as recorded by  
  • Review of Paratesticular Appendageal Tumors, Morphology, Immunohistochemistry, and Recent Molecular Advances
    Mathew Vega, Muhammad T. Idrees
    Surgical Pathology Clinics.2025; 18(1): 119.     CrossRef
  • Cistoadenoma Mucinoso Paratesticular: Caso Interesante en el Instituto Guatemalteco de Seguridad Social
    Edgar Estuardo González López, Carlos Gonzalo Estrada Pazos
    Revista Guatemalteca de Urología.2023; 10(2): 16.     CrossRef
  • Primary borderline mucinous tumor of the testis with postoperative metastasis: A rare case report
    Yingyu Shi, Ling Song, Yan Luo
    Radiology Case Reports.2023; 18(9): 3203.     CrossRef
  • Case report: Misdiagnosis of primary mucinous cystadenoma of the testicle by ultrasound
    Linlin Zhang, Jianyuan Xuan, Manxi Li, Mei Zhang, Yu Song, Ziang Pan, Bo Fan, Lin Lu, Hongyan Zhou, Yang Li
    Frontiers in Oncology.2023;[Epub]     CrossRef
  • Primary Borderline Mucinous Testicular Tumor: A Case Report and Literature Review
    Changjuan Hao, Chunsong Kang, Xiaoyan Kang, Zhuanzhuan Yu, Tingting Li, Jiping Xue
    Frontiers in Oncology.2021;[Epub]     CrossRef
  • Ovarian-type Tumors (Mullerian Tumors) of the Testis: Clinicopathologic Findings with Recent Advances
    Michelle S Lin, Alberto G Ayala, Jae Y Ro
    annals of urologic oncology.2019; : 1.     CrossRef
  • Borderline Mucinous Testicular Tumour: Diagnostic and Management difficulties
    Krishan Pratap, Marlon Perera, Frances Malczewski, Rachel Esler
    BMJ Case Reports.2018; 2018: bcr-2017-223787.     CrossRef
  • Mucinous tumor arising in a giant sacrococcygeal teratoma
    Fengtian Zhang, Xiaolong Yu, Jin Zeng, Min Dai
    Medicine.2017; 96(47): e8759.     CrossRef
Oncocytic Lipoadenoma: A Rare Case of Parotid Gland Tumor and Review of the Literature
Chen-lin Chi, Tseng-tong Kuo, Li-yu Lee
J Pathol Transl Med. 2015;49(2):144-147.   Published online March 12, 2015
DOI: https://doi.org/10.4132/jptm.2014.02.10
  • 11,086 View
  • 69 Download
  • 8 Web of Science
  • 8 Crossref
AbstractAbstract PDF
Oncocytic lipoadenoma is a rare tumor, with only 18 cases having been reported since the first in 1998. We encountered a case of oncocytic lipoadenoma presenting as a slowly growing parotid mass in a 71-year-old man. This tumor is characteristically comprised of a mixture of oncocytes and adipocytes. The present case is one of five reported cases of oncocytic lipoadenoma showing sebaceous differentiation. The results of immunohistochemical study with DOG1 antibody supported the origination of this tumor in the striated duct.

Citations

Citations to this article as recorded by  
  • Oncocytic lipoadenoma of the parotid gland: a case report and a review of the literature
    Jood K Alotaibi, Turki Mohammed Almuhaimid, Ghada Abdallah Moumneh
    Journal of Surgical Case Reports.2024;[Epub]     CrossRef
  • Oncocytic sialolipoma of parotid gland: Case report and literature review
    VenuPatel Sureja, KoyyeRavindranath Tagore
    Indian Journal of Pathology and Microbiology.2023; 66(3): 591.     CrossRef
  • Complex Component of Oncocytic and Non-Oncocytic Lipoadenomas in the Parotid Gland: A Case Report
    Fuyuki Sato, Takashi Nakajima, Takashi Sugino
    Diagnostics.2021; 11(8): 1478.     CrossRef
  • Oncocyitic lipoadenoma of the parotid gland
    Renato PIANTANIDA, Alberto CARANTI, Adele CHIESA, Jessica BARIZZI, Ulrike PERRIARD, Filippo BARUCCA, Antonio PELLANDA
    Otorinolaringologia.2021;[Epub]     CrossRef
  • A case of oncocytic lipoadenoma of the submandibular gland and its diagnostic cytology challenges
    Khaled A. Murshed, Ammar Khalafalla, Belal Alani, Hanan Farghaly, Moustafa Alkhalil
    Diagnostic Cytopathology.2020; 48(4): 364.     CrossRef
  • An extremely rare case of giant oncocytic adenolipoma of the parotid gland
    Dipesh Shakya, Ajit Nepal
    Clinical Case Reports.2020; 8(12): 2390.     CrossRef
  • A rare cause of primary hyperparathyroidism: Parathyroid lipoadenoma
    Sabri Özden, Servet Güreşci, Barış Saylam, Gül Dağlar
    Auris Nasus Larynx.2018; 45(6): 1245.     CrossRef
  • Oncocytic osteolipoadenoma of the submandibular gland
    Domenico Corradi, Rodolfo Monaco, Giulia D'Angelo, Paola Bini, Teore Ferri, Enrico M Silini
    Histopathology.2016; 69(1): 148.     CrossRef
Brief Case Report
Cytokeratin-Positive Gastrointestinal Stromal Tumor of Biphasic Morphology: A Case Report
Sung Sun Kim, Yoo Duk Choi, Jae Hyuk Lee, Chan Choi
Korean J Pathol. 2014;48(5):375-378.   Published online October 27, 2014
DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.5.375
  • 8,719 View
  • 39 Download
  • 2 Crossref
PDF

Citations

Citations to this article as recorded by  
  • CYTOKERATINS: NOT AN EPITHELIAL ENTITY ANYMORE?
    Geetpriya Kaur, Devicharan Shetty, Seema Sikka, Aparna Pathak
    INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH.2022; : 15.     CrossRef
  • Gastrointestinal stromal tumors of the stomach in a 10-year-old child
    Saeed Nasher, Fayed Al-Yousofy, Faisal Ahmed
    Journal of Pediatric Surgery Case Reports.2021; 74: 102044.     CrossRef
Case Study
Development of Six Tumors in a Sebaceus Nevus of Jadassohn: Report of a Case
Serap Gozel, Melahat Donmez, Noyan Can Akdur, Hulya Yikilkan
Korean J Pathol. 2013;47(6):569-574.   Published online December 24, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.6.569
  • 10,700 View
  • 94 Download
  • 22 Crossref
AbstractAbstract PDF

Nevus sebaceus of Jadassohn is a congenital cutaneous hamartoma comprised of multiple skin structures. It has the potential to develop into variety of neoplasms of various epidermal adnexal origins. While multiple tumors may occasionally arise, it is unusual for more than four tumors to arise simultaneously within a single sebaceus nevus. Here in, we report a case of a 70-year-old woman with six neoplastic proliferations including a syringocystadenoma papilliferum, pigmented trichoblastoma, tubular apocrine adenoma, sebaceoma, tumors of follicular infundibulum and superficial epithelioma with sebaceus differentiation arising in a long standing nevus sebaceus on the scalp. Our case is extraordinary because a single nevus sebaceus contained six neoplastic proliferations with differentiation toward the folliculosebaceous-apocrine unit.

Citations

Citations to this article as recorded by  
  • Melanotrichoblastoma Arising on Nevus Sebaceous: A Rare Occurence
    Apaopa J. Thekho, Deepika Uikey, Shanta Passi, V. Ramesh
    Indian Journal of Dermatology.2025; 70(2): 105.     CrossRef
  • Co-occurrence of Tubular Apocrine Adenoma and Syringocystadenoma Papilliferum over the Hypogastrium: A Rare Case Report
    R Raghunatha Reddy, Mukunda Ranga Swaroop, Yogesh Devaraj, Greeshma Jagadish, Namratha Govindaraju
    Clinical Dermatology Review.2025; 9(1): 69.     CrossRef
  • Tumor of follicular infundibulum – reappraisal in a series of 28 patients with critical review of the literature
    Michael Wilk, Bettina G. Zelger, Bernhard Zelger
    JDDG: Journal der Deutschen Dermatologischen Gesellschaft.2024; 22(2): 223.     CrossRef
  • Tumor des follikulären Infundibulums – Neubewertung in einer Serie von 28 Patienten mit kritischer Analyse der Literatur
    Michael Wilk, Bettina G. Zelger, Bernhard Zelger
    JDDG: Journal der Deutschen Dermatologischen Gesellschaft.2024; 22(2): 223.     CrossRef
  • Adnexal neoplasms of the eye
    Roman Drozdowski, Jane M. Grant-Kels, Madina Falcone, Campbell L. Stewart
    Clinics in Dermatology.2024; 42(4): 321.     CrossRef
  • Melanotrichoblastoma: sixth case report in the literature
    Juliana Polizel Ocanha-Xavier, José Cândido Caldeira Xavier-Júnior
    Anais Brasileiros de Dermatologia.2023; 98(6): 871.     CrossRef
  • Multiple secondary neoplasms in nevus sebaceus excision
    Travis S. Dowdle, David A. Mehegran, Dylan Maldonado, Cort D. McCaughey
    Baylor University Medical Center Proceedings.2022; 35(2): 241.     CrossRef
  • Congenital tumors arising from nevus sebaceous in 2 neonates
    Lynette Wei Yi Wee, Bori Born, Sharon Mun Yee Wong, Hui-Ling Chia, Sithach Mey, Suresh Chandran, Mark Jean Aan Koh
    JAAD Case Reports.2022; 21: 70.     CrossRef
  • Development of seven secondary neoplasms in a nevus sebaceous: a case report and literature review
    Yi-Wen Kuo, Jung-Chia Lin, Wei-Hsuan Tsai
    Archives of Craniofacial Surgery.2022; 23(2): 83.     CrossRef
  • Multiple rare neoplasms arising from the nevus sebaceous of the scalp: A case report
    Deepthi Shetty, Anilkumar Desai, Niranjan Kumar, Dinesh U.S., Aditya Agnihotri, Saurav Bhaduri
    Gulhane Medical Journal.2022; 64(2): 197.     CrossRef
  • Syringocystadenoma Papilliferum and Basal Cell Carcinoma Arising in Nevus Sebaceous
    Jingjing Jiang, Yujuan Chen, Qi He, Jiao Yang, Zhengzhong Zhang, Hao Yang, Huan Zhang, Chuan Yang
    Clinical, Cosmetic and Investigational Dermatology.2022; Volume 15: 2021.     CrossRef
  • Eyelid trichoblastoma – A case series
    Gunja Chowdhury, Meghana Tanwar, Usha Kim, Shanthi R. Krishnan
    Journal of Clinical Ophthalmology and Research.2021; 9(3): 123.     CrossRef
  • Trilogy Revisited
    Anand Bardia, Debajyoti Chatterjee, Keshavamurthy Vinay
    Indian Dermatology Online Journal.2021; 12(4): 577.     CrossRef
  • Trichilemmoma coexisting with sebaceous nevus
    AngooriG Rao, VangaliS Reddy, M Tejal, M Divya
    Indian Dermatology Online Journal.2020; 11(2): 253.     CrossRef
  • Syndromic sebaceous nevus: current findings
    Oumama El Ezzi, Anthony S. de Buys Roessingh, Michèle Bigorre, Guillaume Captier
    International Journal of Dermatology.2018; 57(5): 599.     CrossRef
  • Syringocystadenoma papilliferum and trichoblastoma arising in the nevus sebaceous
    Feifei Wang, Yatong Wu, Zhancai Zheng, Yanping Bai
    Indian Journal of Pathology and Microbiology.2018; 61(1): 106.     CrossRef
  • Dermoscopic Analysis of Nevus Sebaceus of Jadassohn: A Study of 13 Cases
    Awatef Kelati, Hanane Baybay, Salim Gallouj, Fatima Zahra Mernissi
    Skin Appendage Disorders.2017; 3(2): 83.     CrossRef
  • Secondary neoplasms arising from nevus sebaceus: A retrospective study of 450 cases in Taiwan
    Ming‐Chun Hsu, Jau‐Yu Liau, Jin‐Liern Hong, Yin Cheng, Yi‐Hua Liao, Jau‐Shiuh Chen, Yi‐Shuan Sheen, Jin‐Bon Hong
    The Journal of Dermatology.2016; 43(2): 175.     CrossRef
  • A Histological Snapshot of Hypothetical Multistep Progression From Nevus Sebaceus to Invasive Syringocystadenocarcinoma Papilliferum
    Vishwas Parekh, Cesar E. Guerrero, Charles F. Knapp, Craig A. Elmets, Kristopher M. McKay
    The American Journal of Dermatopathology.2016; 38(1): 56.     CrossRef
  • Trichoblastoma, syringocystadenoma papilliferum, desmoplastic trichilemmoma and tumor of the follicular infundibulum with signet‐ring cells, all arising in nevus sebaceus
    Emilie Dore, Megan H. Noe, Brian L. Swick
    Journal of Cutaneous Pathology.2015; 42(9): 645.     CrossRef
  • Ceruminous adenoma (ceruminoma) arising in a nevus sebaceus of Jadassohn within the external auditory canal of a 3 year-old boy – A case report
    Elżbieta Niemczyk, Kazimierz Niemczyk, Jadwiga Małdyk, Lidia Zawadzka-Głos
    International Journal of Pediatric Otorhinolaryngology.2015; 79(11): 1932.     CrossRef
  • Fehlbildungen und Nävi des behaarten Kopfes
    V. Behle, H. Hamm
    Der Hautarzt.2014; 65(12): 1022.     CrossRef
Original Article
Clinicopathological Analysis of Hepatocellular Adenoma According to New Bordeaux Classification: Report of Eight Korean Cases
Hyunchul Kim, Ja-June Jang, Dong-Sik Kim, Beom Woo Yeom, Nam Hee Won
Korean J Pathol. 2013;47(5):411-417.   Published online October 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.5.411
  • 9,979 View
  • 49 Download
  • 7 Crossref
AbstractAbstract PDF
Background

Hepatocellular adenoma (HCA) is a rare benign tumor of the liver. A subtype classification of HCA (hepatocyte nuclear factor 1α [HNF1α]-mutated, β-catenin-mutated HCA, inflammatory HCA, and unclassified HCA) has recently been established based on a single institutional review of a HCA series by the Bordeaux group.

Methods

We used histologic and immunohistochemical parameters to classify and evaluate eight cases from our institution. We evaluated the new classification method and analyzed correlations between our results and those of other reports.

Results

Seven of our eight cases showed histologic and immunohistochemical results consistent with previous reports. However, one case showed overlapping histologic features, as previously described by the Bordeaux group. Four cases showed glutamine synthetase immunohistochemical staining inconsistent with their classification, indicating that glutamine synthetase staining may not be diagnostic for β-catenin-mutated HCA. HNF1α-mutated HCA may be indicated by the absence of liver fatty acid binding protein expression. Detection of amyloid A may indicate inflammatory HCA. HCA with no mutation in the HNF1α or β-catenin genes and no inflammatory protein expression is categorized as unclassified HCA.

Conclusions

Although the new classification is now generally accepted, validation through follow-up studies is necessary.

Citations

Citations to this article as recorded by  
  • Perinatal Management of Hepatic Adenomas
    Megan A. Nocita, Carla W. Brady, Jeffrey A. Kuller, Luke A. Gatta
    Obstetrical & Gynecological Survey.2024; 79(12): 735.     CrossRef
  • Relevance of morphological features for hepatocellular adenoma classification in pathology practice
    Carla Henriques Agostini, Osmar Damasceno Ribeiro, Arlete Fernandes, Adriana Caroli-Bottino, Vera Lucia Pannain
    Surgical and Experimental Pathology.2020;[Epub]     CrossRef
  • The molecular functions of hepatocyte nuclear factors – In and beyond the liver
    Hwee Hui Lau, Natasha Hui Jin Ng, Larry Sai Weng Loo, Joanita Binte Jasmen, Adrian Kee Keong Teo
    Journal of Hepatology.2018; 68(5): 1033.     CrossRef
  • Hepatocellular adenoma: Classification, variants and clinical relevance
    Paulette Bioulac-Sage, Christine Sempoux, Charles Balabaud
    Seminars in Diagnostic Pathology.2017; 34(2): 112.     CrossRef
  • A Limited Immunohistochemical Panel Can Subtype Hepatocellular Adenomas for Routine Practice
    Brent K. Larson, Maha Guindi
    American Journal of Clinical Pathology.2017; 147(6): 557.     CrossRef
  • Hepatocellular Neoplasms Arising in Association With Androgen Use
    Sounak Gupta, Bita V. Naini, Richard Munoz, Rondell P. Graham, Benjamin R. Kipp, Michael S. Torbenson, Taofic Mounajjed
    American Journal of Surgical Pathology.2016; 40(4): 454.     CrossRef
  • Pigmented hepatocellular adenomas have a high risk of atypia and malignancy
    Taofic Mounajjed, Saba Yasir, Patrice A Aleff, Michael S Torbenson
    Modern Pathology.2015; 28(9): 1265.     CrossRef
Case Study
Sebaceous Carcinoma Arising in Mature Cystic Teratoma of Ovary
Hyo Jeong An, Yong Han Jung, Hye Kyoung Yoon, Soo Jin Jung
Korean J Pathol. 2013;47(4):383-387.   Published online August 26, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.4.383
  • 8,925 View
  • 69 Download
  • 11 Crossref
AbstractAbstract PDF

Roughly 1% of mature cystic teratomas undergo malignant transformation. In particular, cutaneous-type adnexal neoplasms may occur in mature cystic teratomas. Sebaceous carcinomas, which arise from mature cystic teratomas, have rarely been observed, with only seven cases previously reported. Here, we present a case of a 69-year-old female who had pelvic pain for two weeks and who subsequently underwent bilateral salpingo-oophorectomy and hysterectomy. Her left ovary showed a unilocular cyst, measuring 22.0 cm in diameter, filled with sebaceous material and a few hairs. A luminally-protruding solid mass measuring 4.0 cm in diameter was also noted. Microscopic findings revealed lobular or diffusely arranged basophilic, atypical sebaceous cells connected to a typical mature cystic teratoma. Tumor cells demonstrated positive immunoreactivity for high molecular weight cytokeratin, cytokeratin 7, cytokeratin 19, epithelial membrane antigen, and carcinoembryonic antigen. Here, we present a case of sebaceous carcinoma arising from a mature cystic teratoma along with a review of previously published reports.

Citations

Citations to this article as recorded by  
  • How can we best manage ovarian sebaceous carcinomas arising from mature cystic teratomas?
    Hong Min Shaye Peng, Sung Hock Chew, Yang Huang Grace Ng, Felicia Hui Xian Chin
    BMJ Case Reports.2025; 18(2): e264651.     CrossRef
  • Genetic Profiling of Sebaceous Carcinoma Arising from an Ovarian Mature Teratoma: A Case Report
    Sumika Zaitsu, Yoko Aoyagi, Haruto Nishida, Kohei Nakamura, Mitsutake Yano, Eiji Kobayashi
    International Journal of Molecular Sciences.2024; 25(12): 6351.     CrossRef
  • Extraocular sebaceous carcinoma arising in a mature cystic teratoma of ovary: A case report and review of literature
    Sara Pakbaz, Tanya Chawla, Marcus Q Bernardini, Liat Hogen, Marjan Rouzbahman
    Human Pathology Reports.2022; 27: 300592.     CrossRef
  • Sebaceous adenoma occurring within an intracranial dermoid cyst
    Takashi Minamisaka, Johji Imura, Keitaro Shiraishi, Kohji Takagi, Takahiko Tomia, Sinichi Tanaka, Akira Noguchi, Takuya Akai, Kyo Noguchi, Satoshi Kuroda
    Neuropathology.2022; 42(4): 289.     CrossRef
  • Malignant transformation of mature cystic teratoma of the ovary
    Doaa Atwi, Maria Kamal, Michael Quinton, Lewis A. Hassell
    Journal of Obstetrics and Gynaecology Research.2022; 48(12): 3068.     CrossRef
  • Sebaceous Carcinoma Arising in Ovarian Teratoma: First Report Associated With Germline Mismatch Repair Gene Mutation
    Jacinta Murray, Patrick McIlwaine, Patrick J. Morrison, W. Glenn McCluggage
    International Journal of Gynecological Pathology.2022; 41(6): 608.     CrossRef
  • Impact of surgery and adjuvant treatment on the outcome of extraocular sebaceous carcinoma: a systematic review and individual patient's data analysis of 206 cases
    Prashanth Giridhar, Lakhan Kashyap, Supriya Mallick, Ashish Dutt Upadhyay, Goura K. Rath
    International Journal of Dermatology.2020; 59(4): 494.     CrossRef
  • Mismatch repair deficiency is implicated in carcinoma arising from ovarian teratoma
    Alvin Ho-Kwan Cheung, Chit Chow, Mei-Yung Yu, Wendy Wai-Tak Law, Peggy Pui-Ying Law, Paul Cheung-Lung Choi, Wei Kang, Ka-Fai To
    Pathology.2019; 51(1): 67.     CrossRef
  • Malignant transformation of an ovary mature cystic teratoma: case report and review of the literature
    Elkin Fabián Dorado-Roncancio, Oscar Joel Carrillo-Garibaldi
    Obstetrics & Gynecology International Journal.2019;[Epub]     CrossRef
  • A case of ovarian clear cell carcinoma arising from ovarian mature cystic teratoma
    Kazuya Maeda, Yoshito Terai, Shinichi Terada, Hiroshi Maruoka, Yuhei Kogata, Keisuke Ashihara, Yoshimichi Tanaka, Tomohito Tanaka, Hiroshi Sasaki, Satoshi Tsunetoh, Takashi Yamada, Masahide Ohmichi
    Journal of Ovarian Research.2018;[Epub]     CrossRef
  • Sebaceous carcinoma arising within an ovarian mature cystic teratoma: A case report with discussion of clinical management and genetic evaluation
    Alyssa Wield, Melissa Hodeib, Mohammad Khan, Lindsay Gubernick, Andrew J. Li, Shivani Kandukuri
    Gynecologic Oncology Reports.2018; 26: 37.     CrossRef
Review
Current Concepts and Occurrence of Epithelial Odontogenic Tumors: I. Ameloblastoma and Adenomatoid Odontogenic Tumor
Suk Keun Lee, Yeon Sook Kim
Korean J Pathol. 2013;47(3):191-202.   Published online June 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.3.191
  • 31,444 View
  • 491 Download
  • 41 Crossref
AbstractAbstract PDF

Ameloblastomas and adenomatoid odontogenic tumors (AOTs) are common epithelial tumors of odontogenic origin. Ameloblastomas are clinico-pathologically classified into solid/multicystic, unicystic, desmoplastic, and peripheral types, and also divided into follicular, plexiform, acanthomatous, granular types, etc., based on their histological features. Craniopharyngiomas, derived from the remnants of Rathke's pouch or a misplaced enamel organ, are also comparable to the odontogenic tumors. The malignant transformation of ameloblastomas results in the formation of ameloblastic carcinomas and malignant ameloblastomas depending on cytological dysplasia and metastasis, respectively. AOTs are classified into follicular, extrafollicular, and peripheral types. Ameloblastomas are common, have an aggressive behavior and recurrent course, and are rarely metastatic, while AOTs are hamartomatous benign lesions derived from the complex system of the dental lamina or its remnants. With advances in the elucidation of molecular signaling mechanisms in cells, the cytodifferentiation of epithelial tumor cells in ameloblastomas and AOTs can be identified using different biomarkers. Therefore, it is suggested that comprehensive pathological observation including molecular genetic information can provide a more reliable differential diagnosis for the propagation and prognosis of ameloblastomas and AOTs. This study aimed to review the current concepts of ameloblastomas and AOTs and to discuss their clinico-pathological features relevant to tumorigenesis and prognosis.

Citations

Citations to this article as recorded by  
  • Metabolic Analysis of Tumor Cells Within Ameloblastoma at the Single‐Cell Level
    Rui‐Fang Li, Yi Zhao, Qi‐Wen Man
    Oral Diseases.2025; 31(7): 2206.     CrossRef
  • Granular cell ameloblastoma: A rare case report with public health implications
    Shyamkumar Sriram, Shamimul Hasan, Mambakkam Jayakanth, Syed Ansar Ahmad, Anoop Kumar Narayanan
    Medicine.2025; 104(19): e41992.     CrossRef
  • Exploratory Advanced Radiotherapies for Ameloblastoma and Ameloblastic Carcinoma—A Concise Review
    Heba Turkstani, Afrah Alfaifi, Sunday O. Akintoye
    Oral Diseases.2025; 31(10): 2848.     CrossRef
  • An incidentally discovered interradicular radiolucency of the anterior mandible
    Joshua S. Goldfaden, Joanne L. Prasad, Husniye Demirturk, Steven C. Licht, Richard J. Vargo
    The Journal of the American Dental Association.2025;[Epub]     CrossRef
  • Adenomatoid odontogenic tumor: clinicopathological analysis of 34 cases from Karachi, Pakistan
    Summaya Zafar, Sehar Sulaiman, Madeeha Nisar, Poonum Khan, Nasir Ud Din
    Journal of Pathology and Translational Medicine.2025; 59(6): 390.     CrossRef
  • Differential Profile of Primary and Recurrent Ameloblastomas Among Afro-descendants and Non-Afro-descendants—a Systematic Review
    Parth Patel, Olajumoke A. Effiom, Abdul-Warith O. Akinshipo, Sunday O. Akintoye
    Journal of Racial and Ethnic Health Disparities.2024; 11(1): 92.     CrossRef
  • Adenomatoid Odontogenic Tumor: A 33-Year Retrospective Study with SEM Insight
    Sandhya Tamgadge, Avinash Tamgadge, Treville Pereira, Hritika Mehta, Divya More
    Journal of Microscopy and Ultrastructure.2024;[Epub]     CrossRef
  • Hybrid Ameloblastoma of Jaw-A Case Report
    Sudipa Ghosh, Shivaprasad S., Ashok L., Shambulingappa P.
    Journal of Indian Dental Association.2024;[Epub]     CrossRef
  • Role of HIF-1α in Ameloblastoma: A Systematic Review
    Ayushi Jain, Pooja Sharma, N Sivakumar, Priya Devi, Shalini Gupta, Shaleen Chandra
    Indian Journal of Otolaryngology and Head & Neck Surgery.2023; 75(4): 3136.     CrossRef
  • Machine learning-based radiomics for predicting BRAF-V600E mutations in ameloblastoma
    Wen Li, Yang Li, Xiaoling Liu, Li Wang, Wenqian Chen, Xueshen Qian, Xianglong Zheng, Jiang Chen, Yiming Liu, Lisong Lin
    Frontiers in Immunology.2023;[Epub]     CrossRef
  • Clinicopathological relevance of BRAF and SMO mutations in Chinese patients with ameloblastoma
    Chen Ruixue, Li Hexiang, Hou Yali, Li Xiangjun, Sun Xu, Wang Jie, Zhang Xudong
    All Life.2023;[Epub]     CrossRef
  • Immunohistochemical expression of Ki-67 and Glypican-3 to distinguish aggressive from nonaggressive benign odontogenic tumors
    T. P. Chaturvedi, Kanupriya Gupta, Rahul Agrawal, P. G. Naveen Kumar, Jatin Gupta
    Journal of Cancer Research and Therapeutics.2022; 18(Suppl 2): S205.     CrossRef
  • Hypoxia enhances basal autophagy of epithelial‐derived ameloblastoma cells
    Anwar A. A. Y. AlMuzaini, Kathleen Boesze‐Battaglia, Faizan Alawi, Sunday O. Akintoye
    Oral Diseases.2022; 28(8): 2175.     CrossRef
  • Giant ameloblastoma
    Muthuvel Ramesh, A. N. Gurumoorthy, Jeevan G. Sanjive
    Formosan Journal of Surgery.2022; 55(1): 27.     CrossRef
  • Hemangiomatous Ameloblastoma with Spindle Cell Proliferation: A Rare Case Report and Review of Literature
    Pavan D Puri, Abhinandh Krishna, Suchitra Gosavi, Vivek Nayyar
    Journal of Oral and Maxillofacial Pathology.2022; 26(1): 132.     CrossRef
  • Clinical, Radiographic and Histopathological Analysis of Craniopharyngiomas and Ameloblastomas: A Systematic Review
    Luana Amorim Morais da Silva, Solimar Ribeiro Carlete Filho, Marcelo Jales Diniz Saraiva, Caio Rodrigues Maia, Camila Dannyelle Fernandes Dutra Pe Santos, Pedro Paulo de Andrade Santos
    Head and Neck Pathology.2022; 16(4): 1195.     CrossRef
  • CDC7 Expression in Selected Odontogenic Tumors
    Zohreh Jaafari-Ashkavandi, Nahid Alizadeh, Luca Testarelli
    International Journal of Dentistry.2022;[Epub]     CrossRef
  • Immunohistochemical differential expression of p16 proteins in follicular type and plexiform type ameloblastoma
    Haris Budi Widodo, Anung Saptiwulan, Helmi Hirawan, Christiana Cahyani Prihastuti, Tirta Wardana
    Dental Journal (Majalah Kedokteran Gigi).2022; 55(3): 137.     CrossRef
  • Fibroblastic Growth Factor as a Diagnostic and Prognostic Marker in Odontogenic Cysts and Tumors: A Systematic Review
    Gururaj Narayana Rao, Adlin Saroja Rosaian, Gowthami Jawahar, P. Hari Nivas Raj, J. Beryl Rachel, P. Blessing Emmanuel
    Journal of Pharmacy and Bioallied Sciences.2021; 13(Suppl 1): S6.     CrossRef
  • A View of Adenomatoid Odontogenic Tumor in Ameloblastoma: A Hybrid Variant
    Priya Thomas, Sapna Chandran Lathakumari
    Journal of Health Sciences & Research.2021; 12(1): 21.     CrossRef
  • Development and Validation of a Prognostic Nomogram for Postoperative Recurrence-Free Survival of Ameloblastoma
    Yao-Cheng Yang, Jun-Jie Wang, Yun Huang, Wei-Xin Cai, Qian Tao
    Cancer Management and Research.2021; Volume 13: 4403.     CrossRef
  • Peripheral Adenomatoid Odontogenic Tumor — A Rare Cause of Gingival Enlargement: A Case Report with CBCT Findings


    Arun Sadasivan, Roshni Ramesh, Nikhil M Kurien
    Clinical, Cosmetic and Investigational Dentistry.2020; Volume 12: 297.     CrossRef
  • Adenomatoid odontogenic tumour: A rare threat to orthodontic treatment planning
    Laura Han, Alison Downing, David Farr, Kaushik Dasgupta, Duncan Stewart
    Journal of Orthodontics.2019; 46(3): 259.     CrossRef
  • Recurrence of plexiform ameloblastoma as acanthomatous ameloblastoma: A rare case report
    SanatKumar Bhuyan, Ruchi Bhuyan, TapanKumar Sahoo, Pinali Das
    Contemporary Clinical Dentistry.2019; 10(1): 178.     CrossRef
  • Immunoexperssion of cancer stem cell marker (CD44) in ameloblastoma
    Manjushri Madhukar Vanje, Shahela Tanveer, Syed Afroz Ahmed, Shravan Kumar, Tejashree Vanje
    Journal of Oral and Maxillofacial Pathology.2019; 23(3): 400.     CrossRef
  • Unklare Schwellung im Bereich eines Oberkiefereckzahns
    S. H. Baum, C. Loef, D. Baumhoer, C. Mohr
    Der MKG-Chirurg.2018; 11(2): 111.     CrossRef
  • Ameloblastoma Secondary to Third Molar Extraction and Sagittal Split Ramus Osteotomy : A Case Report
    Sung-Tak Lee, Santhiya Iswarya Vinothini Udayakumar, Tae-Geon Kwon, Hong-In Shin, So-Young Choi
    The Korean Journal of Oral and Maxillofacial Pathology.2018; 42(2): 39.     CrossRef
  • Glypican‐3 distinguishes aggressive from non‐aggressive odontogenic tumors: a preliminary study
    Ramon Barreto Mendes, Rosane Borges Dias, Andreia Leal Figueiredo, Clarissa Araújo Gurgel, Manoel Santana Filho, Leonardo Araújo Melo, Marília Trierveiler, Patrícia Ramos Cury, Rosalia Leonardi, Jean Nunes Dos Santos
    Journal of Oral Pathology & Medicine.2017; 46(4): 297.     CrossRef
  • Immunoexpression of BMP-2 and BMP-4 and their receptors, BMPR-IA and BMPR-II, in ameloblastomas and adenomatoid odontogenic tumors
    Marcelo Anderson Barbosa Nascimento, Cassiano Francisco Weege Nonaka, Carlos Augusto Galvão Barboza, Roseana de Almeida Freitas, Leão Pereira Pinto, Lélia Batista de Souza
    Archives of Oral Biology.2017; 73: 223.     CrossRef
  • Rare case of ameloblastoma with pulmonary metastases
    Ivan Valkadinov, Nikolay Conev, Dian Dzhenkov, Ivan Donev
    Intractable & Rare Diseases Research.2017; 6(3): 211.     CrossRef
  • High strength oil palm shell concrete beams reinforced with steel fibres
    S. Poh-Yap, U. Johnson-Alengaram, K. Hung-Mo, M. Zamin-Jumaat
    Materiales de Construcción.2017; 67(328): e142.     CrossRef
  • A novel marker of ameloblastoma and systematic review of immunohistochemical findings
    Bacem A.E.O. Khalele, Rami A. Al-Shiaty
    Annals of Diagnostic Pathology.2016; 22: 18.     CrossRef
  • Adenoid variant of peripheral ameloblastoma with cellular atypia in the retromolar pad area: A case report
    Bacem A.E.O. Khalele
    Future Dental Journal.2016; 2(2): 91.     CrossRef
  • Ameloblastoma during pregnancy: a case report
    Helbert Eustáquio Cardoso da Silva, Erika do Socorro Ramos Costa, Antônio Carlos Quintão Medeiros, Paulo Sérgio dos Santos Pereira
    Journal of Medical Case Reports.2016;[Epub]     CrossRef
  • A case report and short review on changing trends in the site of occurrence of adenomatoid odontogenic tumor: Unravelling the past 15 years
    Sneha Sethi, Manish Kumar, Pratul Aggarwal, HS Indra Kumar, ChetanD Sugandhi, Silvie Singh
    Dental Research Journal.2016; 13(5): 462.     CrossRef
  • De novo adamantinomatous craniopharyngioma presenting anew in an elderly patient with previous normal CT and MRI studies: A case report and implications on pathogenesis
    Amy Walker, Radmehr Torabi, Michael Punsoni, Edward Stopa, Curtis Doberstein
    Interdisciplinary Neurosurgery.2015; 2(3): 149.     CrossRef
  • Understanding ameloblastomas through tooth development
    Amer Sehic
    Journal of Dentistry and Oral Care.2015;[Epub]     CrossRef
  • New Features in Mucous-Ameloblastoma. A Case Report of rare Entity
    IS Gataa
    International Journal of Oral and Craniofacial Science.2015; : 001.     CrossRef
  • Aggressive granular cell ameloblastoma: Report of a rare case
    N. Aravindha Babu, S. Leena Sankari, N. Anitha, Gouse Mohideen
    Journal of Pharmacy and Bioallied Sciences.2015; 7(Suppl 1): S276.     CrossRef
  • Adenomatoid odontogenic tumor associated with a dentigerous cyst: A case report
    Ludmila de Faro Valverde, Tássia Amaral Gomes, Maria Lúcia Neves, Rosane Borges Dias, Manuela Torres Andion Vidal, Caroline Brandi Schlaepfer Sales, Clarissa Araújo Gurgel Rocha, Jean Nunes dos Santos
    Indian Journal of Dentistry.2014; 5: 82.     CrossRef
  • Adenomatoid odontogen tumor: «To tredje-delstumoren»
    Bjarte Grung, Anne Christine Johannessen
    Den norske tannlegeforenings Tidende.2014; 124(9): 740.     CrossRef
Case Reports
Parathyromatosis: Critical Diagnosis Regarding Surgery and Pathologic Evaluation
Ayşegül Aksoy-Altinboga, Ayşegül Akder Sari, Türkan Rezanko, Mehmet Haciyanli, Aylin Orgen Calli
Korean J Pathol. 2012;46(2):197-200.   Published online April 25, 2012
DOI: https://doi.org/10.4132/KoreanJPathol.2012.46.2.197
  • 8,880 View
  • 44 Download
  • 15 Crossref
AbstractAbstract PDF

Parathyromatosis, in which several nodules of hyperfunctioning parathyroid tissue form in the neck and mediastinum, is a rare cause of recurrent hyperparathyroidism. However, there are some theories regarding the origin of parathyromatosis, and seeding after rupture of the parathyroid gland capsule during surgical removal of a parathyroid lesions is the most regarded one. Herein, we report a 41-year-old man who presented with multiple parathyroid nodules in and around the left thyroid lobe 5 years after parathyroid surgery for secondary hyperparathyroidism that was finally diagnosed as parathyromatosis. We discuss the differential diagnosis of parathyromatosis from other parathyroid tumors, particularly from parathyroid carcinoma, which is important in the management of a suspected lesion.

Citations

Citations to this article as recorded by  
  • Parathyromatosis: The Pathogenic Background (Post-Parathyroidectomy Seeding or Exceptional Embryologic Remnant) and the Importance of a Fine Clinical Index for Recurrent Primary Hyperparathyroidism (a Narrative Review)
    Ana-Maria Gheorghe, Claudiu Nistor, Mara Carsote
    Journal of Clinical Medicine.2025; 14(19): 6937.     CrossRef
  • Parathyromatosis: A Challenging Management in a Young Girl Case Report With Literature Review
    Grace Jrad, Rim Masri, Bassam Abboud, Claude Ghorra, Charbel Mourad, Kalyani Sen
    Case Reports in Endocrinology.2025;[Epub]     CrossRef
  • Intractable Parathyromatosis despite extensive surgical interventions: A case report with literature review
    Shada Khaled Bashantoof, Mansoor Abdulmajeed Alramadhan, Modhi Hamad Alawadh, Nada Abdulaziz Bin Samaih, Rania Abdullah Alshammari, Abdulsalam Aodah
    International Journal of Surgery Case Reports.2024; 114: 109172.     CrossRef
  • Late recurrence of a single gland primary hyperparathyroidism—Atypical parathyroid adenoma or misdiagnosed parathyroid carcinoma
    Jessica Kotliarevskaia, Udo Siebolts, Henning Dralle, Frank Schuppert
    Clinical Case Reports.2024;[Epub]     CrossRef
  • Parathyroid Carcinoma Complicated by Parathyromatosis and Refractory Hypercalcemia
    Yug Garg, Madhumati S Vaishnav, Nidhi Garg, Kavitha Muniraj, Sathyanarayana Srikanta
    Cureus.2024;[Epub]     CrossRef
  • Retrosternal parathyromatosis in a patient with prior total parathyroidectomy
    Tariq Saleh, Marwan Alaswad, Abdullah Otry, Waleed Saleh
    Journal of Surgical Case Reports.2023;[Epub]     CrossRef
  • Histological alterations following fine‐needle aspiration for parathyroid adenoma: Incidence and diagnostic problems
    Mitsuyoshi Hirokawa, Ayana Suzuki, Miyoko Higuchi, Toshitetsu Hayashi, Seiji Kuma, Akihiro Miya, Akira Miyauchi
    Pathology International.2021; 71(6): 400.     CrossRef
  • Parathyromatosis as a cause of recurrence primary hyperparathyroidism
    Elena A. Ilyicheva, Gleb A. Bersenev
    International Journal of Surgery Case Reports.2021; 80(C): 105689.     CrossRef
  • Seguridad y rendimiento diagnóstico de la medición de PTH en el lavado del aspirado de lesiones sospechosas de adenomas de paratiroides
    Florentino Carral, Ana Isabel Jiménez, Mariana Tomé, Javier Alvarez, Ana Díez, Concepción García, Vicente Vega, Carmen Ayala
    Endocrinología, Diabetes y Nutrición.2021; 68(7): 481.     CrossRef
  • Safety and diagnostic performance of parathyroid hormone assay in fine-needle aspirate in suspicious parathyroid adenomas
    Florentino Carral, Ana Isabel Jiménez, Mariana Tomé, Javier Alvarez, Ana Díez, Concepción García, Vicente Vega, Carmen Ayala
    Endocrinología, Diabetes y Nutrición (English ed.).2021; 68(7): 481.     CrossRef
  • Persistent secondary hyperparathyroidism caused by parathyromatosis and supernumerary parathyroid glands in a patient on haemodialysis
    Jun Yang, Jun Zhang, Ning-hu Liu, Hao Liu, Meng-jie Dong
    BMC Nephrology.2020;[Epub]     CrossRef
  • Parathyromatosis: A Rare Case of Recurrent Hyperparathyroidism Localized by Four-Dimensional Computed Tomography
    Abraham E. Wei, Matthew R. Garrett, Ankur Gupta
    AACE Clinical Case Reports.2019; 5(6): e384.     CrossRef
  • Parathyromatosis: a very rare cause of recurrent primary hyperparathyroidism – case report and review of the literature
    M Haciyanli, S Karaisli, S Gucek Haciyanli, A Atasever, D Arikan Etit, EO Gur, T Acar
    The Annals of The Royal College of Surgeons of England.2019; 101(8): e178.     CrossRef
  • Parathyromatose : une cause rare d’hyperparathyroïdie récidivante
    I. Achour, S. Charfi, M.A. Chaabouni, A. Chakroun, F. Guermazi, B. Hammami, A. Ghorbel
    La Revue de Médecine Interne.2017; 38(1): 61.     CrossRef
  • Recurrent primary hyperparathyroidism due to Type 1 parathyromatosis
    Monica Jain, David L. Krasne, Frederick R. Singer, Armando E. Giuliano
    Endocrine.2017; 55(2): 643.     CrossRef
Urachal Mucinous Tumor of Uncertain Malignant Potential: A Case Report
Jung-Woo Choi, Ju-Han Lee, Young-Sik Kim
Korean J Pathol. 2012;46(1):83-86.   Published online February 23, 2012
DOI: https://doi.org/10.4132/KoreanJPathol.2012.46.1.83
  • 11,038 View
  • 63 Download
  • 8 Crossref
AbstractAbstract PDF

Urachal mucinous tumor of uncertain malignant potential is very rare and is characterized by a multilocular cyst showing the proliferation of atypical mucin-secreting cells without stromal invasion. As in ovarian and appendiceal borderline tumors, it represents a transitional stage of mucinous carcinogenesis in the urachus. In addition, this tumor may recur locally and develop into pseudomyxoma peritonei. Due to its scarcity and diagnostic challenges, we report a mucinous tumor of uncertain malignant potential arising in the urachus.

Citations

Citations to this article as recorded by  
  • Exploring the Enigma of a Urachal Mucinous Cystic Tumor of Low Malignant Potential (MCTLMP): A Case Report and Literature Review
    Klaas De Corte, Ali Ramadhan
    Cureus.2025;[Epub]     CrossRef
  • Mucinous Cystadenoma of the Urachus and Review of Current Classification of Urachal Mucinous Cystic Neoplasms
    Diping Wang, Norbert Sule
    Archives of Pathology & Laboratory Medicine.2019; 143(2): 258.     CrossRef
  • Urachal Mucinous Cystic Tumor of Low Malignant Potential with Concurrent Sigmoid Colon Adenocarcinoma
    Kelly Brennan, Paul Johnson, Heather Curtis, Thomas Arnason
    Case Reports in Gastrointestinal Medicine.2019; 2019: 1.     CrossRef
  • Pseudomyxoma Peritonei Arising from Mucinous Cystadenoma of the Urachus with Postoperative Disease-Free Survival over 15 Years
    Tomoki Kobayashi, Shinichi Mizuno, Hideki Matsuba, Min Kanamori, Toshio Tamauchi, Makoto Urano
    The Japanese Journal of Gastroenterological Surgery.2019; 52(6): 307.     CrossRef
  • Urachal borderline mucinous cystadenoma
    Jingjun Wu, Ailian Liu, Anliang Chen, Pengxin Zhang
    Medicine.2017; 96(47): e8740.     CrossRef
  • Incidental Finding of a Rare Urachal Pathology: Urachal Mucinous Cystic Tumour of Low Malignant Potential
    Luke L. Wang, Heath Liddell, Sharman Tan Tanny, Briony Norris, Sree Appu, David Pan
    Case Reports in Urology.2016; 2016: 1.     CrossRef
  • A Case of Borderline Mucinous Cystadenoma Thought to be of Urachal Origin
    Kiichiro YAGUCHI, Yoshihito GOMYO, Hiroyasu SAITO, Tatsuo IKENO, Hiromi SAKAGUCHI, Hideo MIYAMOTO
    Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2014; 75(5): 1418.     CrossRef
  • An unexpected mass of the urachus: a case report
    Monica C. Pasternak, Jonathan D. Black, Natalia Buza, Masoud Azodi, Aileen Gariepy
    American Journal of Obstetrics and Gynecology.2014; 211(4): e1.     CrossRef
Original Article
Diagnostic Features of Fine Needle Aspiration Cytology of Pleomorphic Adenoma, Adenoid Cystic Carcinoma, and Mucoepidermoid Carcinoma of Salivary Gland.
Eun Sook Nam, Won Bo Jo, Jung Ho Han, Insun Kim
J Pathol Transl Med. 1990;1(1):60-67.
  • 6,768 View
  • 299 Download
AbstractAbstract PDF
The evaluate the diagnostic findings of salivary gland tumors, we reexamined aspiration cytology smears of 7 cases of pleomorphic adenoma, 3 cases of adenoid cystic carcinoma, and 3 cases of mucoepidermoid carcinoma, performed during April 1986 to March 1990, which were comfurmed by surgical excision and histologic diagnosis. The results obtained are summarized as follows : 1. All cases of pleomorphic adenoma showed branching cellular clusters of epithelial and myoepithelial cells. Acellular elements including myxomatous and chondroid components were observed. There were no cellular pleomorphism and nucleoli. Keratinizing squamous epithelial cells and keratin pearls were noted. 2. The smears of adenoid cystic carcinoma showed cell balls or cell cords containing a central hyaline core. Nuclear atypism and the nucleoli were frequently observed. There were no keratinizing squamous epithelial cells. 3. The smears of mucoepidermoid carcinoma showed mainly sheets or clusters of intermediate cells and some mucin-producing cells. Some nuclear pleomorphism was observed. Mucinous material and many inflammatory cells were present in the background.
Case Reports
Esophageal Gland Duct Adenoma.
Yoonjung Kim, Yang Soon Park, Jei So Bang, Ji Yeon Kim, Young Hyeh Ko, Cheol Keun Park, Kyoung Mee Kim
Korean J Pathol. 2011;45:S45-S47.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.S1.S45
  • 3,716 View
  • 47 Download
AbstractAbstract PDF
Benign ductal or glandular neoplasms of the esophagus unrelated to Barrett esophagus are extremely rare. Only 9 cases have been reported in the English language literature. We now report a case of esophageal gland duct adenoma incidentally found in a 73-year-old man. A 0.8 cm-sized, polypoid submucosal lesion in the distal esophagus was removed. Histologically, the lesion was well circumscribed and consisted of several ducts or cysts with focal papillary configurations. Interstitial lymphocytic infiltration with germinal centers was also observed. The lining cells of ducts or cysts were composed of two layers: an inner intensely eosinophilic luminal duct cell layer and an outer myoepithelial cell layer that was accentuated by alpha-smooth muscle actin. There was no significant nuclear atypia or mitosis. Mucin production was occasionally observed in a few goblet cells. To the best of our knowledge, this is the first case of benign ductal or glandular neoplasm of the esophagus among Koreans.
A Cutaneous Myoepithelial Carcinoma Arising in a Papillary Eccrine Adenoma.
Ji Han Jung, Soyoung Im, Seok Jin Kang, Gyong Moon Kim, Ki Taik Han, Jin Young Yoo, Chang Suk Kang
Korean J Pathol. 2011;45(6):644-649.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.6.644
  • 4,042 View
  • 22 Download
  • 4 Crossref
AbstractAbstract PDF
Cutaneous myoepithelial neoplasms and papillary eccrine adenomas (PEA) are rare conditions. Malignant tumors within a PEA are even rarer, with only one case reported to date. Herein, we present an extremely rare case of a cutaneous myoepithelial carcinoma arising in a PEA in a 70-year-old man presenting a solid mass in the left buttock. Histopathologically, most of the resected tumor revealed features consistent with the diagnosis of PEA. Some small nests and nodules were intermixed with the PEA and were present adjacent to the PEA. The tumor cells of nests and nodules showed ovoid to spindle shaped nuclei and slightly eosinophilic cytoplasm. Immunohistochemically, they were positive for both epithelial and myogenic markers, consistent with myoepithelioma. An inguinal lymph node with a metastatic lesion showed the same findings of myoepithelioma despite inconspicuous atypia. Our case showed malignant transformation of the myoepithelial cells at the outermost layers of the PEA.

Citations

Citations to this article as recorded by  
  • TRPS1::PLAG1 Fusion in a Primary Cutaneous Myoepithelial Carcinoma: A Case Report and Literature Review
    Timber Gillis, Jenika Howell, Fatemeh Jafarian
    Journal of Cutaneous Pathology.2026; 53(2): 169.     CrossRef
  • Papillary eccrine adenoma associated with syringocystadenoma papilliferum
    Neha Meena, PrafullaKumar Sharma, Sawan Kumar, Minakshi Bhardwaj
    Indian Journal of Dermatology, Venereology and Leprology.2018; 84(3): 322.     CrossRef
  • Pleural fluid metastases of myoepithelial carcinoma: A case report and review of the literature
    Alicia Calderon Bhambra, Yanhong Zhang, Eric C. Huang, John Bishop, Mahan Matin, Alaa Afify
    CytoJournal.2016; 13: 13.     CrossRef
  • Myoepithelial carcinoma of buccal mucosa: A rare tumor
    Jeevan Lata, Fahad Ahmad, Vimal Chand
    Contemporary Clinical Dentistry.2014; 5(2): 247.     CrossRef
Original Article
CpG Island Methylation According to the Histologic Patterns of Early Gastric Adenocarcinoma.
Junjeong Choi, Mee Yon Cho, So Young Jung, Khalilullah Mia Jan, Hyun Soo Kim
Korean J Pathol. 2011;45(5):469-476.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.5.469
  • 4,735 View
  • 22 Download
  • 2 Crossref
AbstractAbstract PDF
BACKGROUND
Although the importance of aberrant DNA methylation in the development of gastric adenocarcinoma has been described, the mechanism of pathogenesis has not been revealed yet. We quantitatively analyzed methylation of four CpG islands and one repetitive DNA element, according to the histologic features of adenocarcinoma with precursor lesions.
METHODS
We divided the cases as adenocarcinoma with intestinal type precursors (type A, n=19 cases) and adenocarcinoma with diffuse type precursors (type B, n=19 cases). We micro-dissected tumor cells and matched non-neoplastic gastric mucosa from the hematoxylin and eosin-stained slides.
RESULTS
A total of 20 CpG sites of long interspersed nucleotide element-1 (LINE1), RAR-related orphan receptor alpha (RORA), Kruppel-like factor 7 (KLF7), mutL homolog 1 (MLH1), MINT25, and CD133 were analyzed. Methylation was determined by bisulfate-pyro-sequencing, and hypomethylation of LINE1 and CD133 was noted in the tumors, compared to the levels in the non-neoplastic gastric mucosa (p=0.014 and p=0.015, respectively). A statistically different methylation pattern of CpG sites at CD133 and KLF7 was noted only in type B lesions, compared to that in matched non-neoplastic gastric mucosa (p=0.027 and p=0.043, respectively).
CONCLUSIONS
Given that aberrant methylation occurs in a relatively early phase of carcinogenesis, different patterns of methylation may determine the carcinoma phenotype. However, further large-scale study is required to clarify the significance of this difference.

Citations

Citations to this article as recorded by  
  • Molecular function of Krüppel-like factor 7 in biology
    Yi Mao, Yuechan Chen, Zhiwei Zhang
    Acta Biochimica et Biophysica Sinica.2023; 55(5): 713.     CrossRef
  • DNA methylation status of a distinctively different subset of genes is associated with each histologic Lauren classification subtype in early gastric carcinogenesis
    YOSEP CHONG, KHALILULLAH MIA-JAN, HOON RYU, JAMSHID ABDUL-GHAFAR, JIJGEE MUNKHDELGER, SAYAMAA LKHAGVADORJ, SO YOUNG JUNG, MIRA LEE, SUN-YOUNG JI, EUNHEE CHOI, MEE-YON CHO
    Oncology Reports.2014; 31(6): 2535.     CrossRef
Case Report
Cytologic Features and BRAF Mutation of Hyalinizing Trabecular Adenoma of the Thyroid: A Case Report with Review of the Literature.
Se Min Jang, Young Ha Oh, Yoon Kyung Jeon, Yong Wook Park, Moon Hyang Park
Korean J Pathol. 2011;45(4):428-433.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.4.428
  • 4,467 View
  • 33 Download
  • 2 Crossref
AbstractAbstract PDF
A hyalinizing trabecular adenoma (HTA) is a rare benign thyroid tumor of follicular epithelial cell origin with a trabecular-alveolar growth pattern and marked intratrabecular hyalinization. The cytological and histological features of HTA are very similar to those of papillary and medullary carcinomas of the thyroid. Therefore, an accurate diagnosis of HTA is important to avoid unnecessary and potentially harmful management of patients. However, the results of BRAF gene mutation analysis shown by many studies are distinctly different between HTAs and papillary thyroid carcinomas. Herein, we describe a rare case of HTA of the thyroid in a 49-year-old female and consider its characteristic cytological features and BRAF gene mutation analysis results with a brief review of the literature.

Citations

Citations to this article as recorded by  
  • Hyalinizing trabecular tumor, a rare histologically unique tumor of the thyroid, coexisting with papillary thyroid carcinoma
    Chiu-Hsuan Cheng
    Tzu Chi Medical Journal.2021; 33(2): 198.     CrossRef
  • A Case of Hyalinizing Trabecular Tumor of the Thyroid Gland
    Kun Woo Kim, Sang Joon Lee, Phil-Sang Chung, Junghwan Moon
    Korean Journal of Otorhinolaryngology-Head and Neck Surgery.2012; 55(12): 795.     CrossRef
Original Article
Insulin-like Growth Factor II mRNA-Binding Protein 3 Expression in Benign and Premalignant Lesions and Carcinomas of the Stomach.
Dae Hyun Song, Jung Wook Yang, Dong Chul Kim, Jong Sil Lee, Jeong Hee Lee, Sang Ho Jeong, Gyung Hyuck Ko
Korean J Pathol. 2011;45(4):379-385.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.4.379
  • 4,263 View
  • 25 Download
  • 2 Crossref
AbstractAbstract PDF
BACKGROUND
Recent studies have demonstrated that insulin-like growth factor II mRNA-binding protein 3 (IMP3) is expressed in malignant tumors of various organs but not in normal tissue. We investigated IMP3 expression in various benign lesions, premalignant lesions and carcinomas of the stomach.
METHODS
IMP3 immunohistochemical staining was performed on 24 benign gastric lesions, 24 gastric adenomas, and 322 gastric carcinomas.
RESULTS
IMP3 was not expressed in benign gastric lesions including adenomas with low-grade dysplasia, but was expressed in 17% of adenomas with high-grade dysplasia, and in 44% of carcinomas. As the carcinomas were in the advanced stage, they expressed IMP3 more frequently and strongly. Patients with IMP3-positive tumors had poorer survival than those with negative tumors.
CONCLUSIONS
IMP3 expression in gastric carcinoma may be related to tumor invasion and metastasis, and is an independent risk factor for poor prognosis.

Citations

Citations to this article as recorded by  
  • IMP3, a Promising Prognostic Marker in Clear Cell Renal Cell Carcinoma
    Ji Young Park, Misun Choe, Yuna Kang, Sang Sook Lee
    Korean Journal of Pathology.2014; 48(2): 108.     CrossRef
  • Role of combination of insulin-like growth factor II messenger RNA-binding protein 3 and claudin-1 immunostaining in differentiation between endometrial endometrioid carcinoma and uterine serous carcinoma
    Maha M. Shamloula, Dareen A. Mohamed, Ayman El-Dorf
    Egyptian Journal of Pathology.2013; 33(2): 237.     CrossRef
Case Reports
Cytologic Distinctive Features of Brenner Tumor.
Jung Sik Jang, An Na Seo, Seon Jae Lee, Ji Young Park
Korean J Pathol. 2011;45(2):223-226.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.2.223
  • 4,698 View
  • 33 Download
  • 1 Crossref
AbstractAbstract PDF
Herein, we present two cases of Brenner tumor, a rarely occurring neoplasm in the ovaries, obtained via intraoperative fine needle aspiration. The borderline Brenner tumor exhibited marked squamous metaplasia, characterized by individually distributed atypical squamous cells. A benign Brenner tumor associated with mucinous cystadenoma evidenced typical mucinous metaplastic features and transitional foci. These distinctive features may prove helpful in differential diagnosis of varied ovarian tumors, and particularly for intraoperative consultation.

Citations

Citations to this article as recorded by  
  • Pre‐operative cytodiagnosis of an adult granulosa cell tumour: report of a case with its differential diagnosis
    S. R. Jinkala, S. E. Jacob, S. Neelaiah, B. A. Badhe
    Cytopathology.2014; 25(1): 63.     CrossRef
Functional Adrenocortical Oncocytoma: A Case Report of Rare Neoplasm of Uncertain Malignant Potential.
Jamshid Abdul-Ghafar, Keum Seok Bae, Kwang Hwa Park
Korean J Pathol. 2011;45(2):212-216.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.2.212
  • 3,769 View
  • 26 Download
AbstractAbstract PDF
Adrenocortical oncocytoma is a rare adrenal neoplasm with only 25 cases having been reported in the English medical literature, of which only seven were functional tumors. Since these adrenal tumors are usually nonfunctional, they are mostly incidentally detected, and most of them are benign. Herein, we report on a rare case of a functional adrenocortical oncocytoma of an uncertain malignant potential and this tumor was located in the left adrenal gland in a 59-year-old woman who presented with hypertension. The tumor size was large with foci of necrosis in the cut surface and it exclusively had oncocytic histologic features.
Adrenal Cortical Adenoma Developed in Adrenohepatic Fusion, a Mimicry of Hepatocellular Carcinoma: A Case Report.
Sun A Kim, Young Joo Lee, Kyoung Won Kim, Gyungyub Gong
Korean J Pathol. 2011;45(2):196-200.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.2.196
  • 5,171 View
  • 42 Download
  • 4 Crossref
AbstractAbstract PDF
Adrenohepatic fusion is the union of the liver and adrenal gland with close intermingling of their respective parenchymal cells. Adrenal cortical adenoma arising in adrenohepatic fusion tissue is extremely rare, although adrenohepatic fusion itself is relatively common. Here we report a case of a 59-year-old man with a mass in the right lobe of his liver. The mass showed slight hyperattenuation during arterial phase and hypoattenuation during portal phase on dynamic computed tomography with contrast enhancement. On pathology, the mass consisted of round to polygonal cells with clear microvesicular or eosinophilic cytoplasm, arranged in nests or in a trabecular pattern. The tumor cells were positive for inhibin and melan-A, but negative for Hep Par-1. In the periphery of the mass, adrenohepatic fusion was identified between the liver and adrenal gland, and was simultaneously resected with the mass. We report this rare case, and discuss its clinical implications, especially the differential diagnosis with hepatocellular carcinoma.

Citations

Citations to this article as recorded by  
  • An intrahepatic adrenal adenoma mimicking hepatocellular carcinoma: A case report and literature review
    Cheng-Ju Yang, Cheng-Ming Peng
    Formosan Journal of Surgery.2025; 58(5): 222.     CrossRef
  • Adrenal cortical adenoma arising in an adreno-hepatic fusion: Case report and literature review of a potential diagnostic pitfall
    Adam Stenman, Ivan Shabo, Jan Zedenius, C. Christofer Juhlin
    Human Pathology Reports.2022; 29: 300656.     CrossRef
  • Intrahepatic adrenocortical adenoma arising from adrenohepatic fusion mimicking hepatic malignancy
    Yong Soo Cho, Jin Woong Kim, Hyun Ju Seon, Ju-Yeon Cho, Jun-Hee Park, Hyung Joong Kim, Yoo Duk Choi, Young Hoe Hur
    Medicine.2019; 98(23): e15901.     CrossRef
  • Direct and indirect imaging features of adrenohepatic fusion
    Jung Jae Park, Byung Kwan Park, Chan Kyo Kim
    Abdominal Radiology.2016; 41(2): 377.     CrossRef
Coexistence of Intrapulmonary Bronchogenic Cyst and Congenital Cystic Adenomatoid Malformation: A Case Report.
Mee Hye Oh, Eun Ah Jung, Ji Hye Lee, Hyun Deuk Cho, Ki Hyun Seo, Seock Yeol Lee, Young Tong Kim
Korean J Pathol. 2011;45(1):92-95.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.1.92
  • 3,722 View
  • 23 Download
  • 1 Crossref
AbstractAbstract PDF
Congenital cystic lesions of the lung are uncommon and a conjunction of two or more lesions is very rare. We report here on a case of coexisting intrapulmonary bronchogenic cyst and congenital cystic adenomatoid malformation in a 13-year-old female with a cystic mass in the right upper lobe of the lung. Computed tomography showed a cystic lesion measuring 2.5 cm with an air fluid level and surrounding multicystic lesions in the right upper lobe. On gross examination, the cut surface showed a cystic mass containing inspissated mucinous material, and the cystic mass was surrounded by multiple small cysts. Microscopically, the larger cystic cavity was lined with pseudostratified ciliated columnar epithelium. The submucosal tissue contained mucinous glands and plates of cartilage. The surrounding smaller cysts or irregular spaces were lined with bronchiolar-type respiratory epithelium. We propose that this hybrid lung lesion may represent the missing link in a common embryologic pathway determined by the timing of mesenchymal and epithelial interactions.

Citations

Citations to this article as recorded by  
  • Case 2: Coexisting Cystic Lesions of Lung in a Term Neonate: A Management Dilemma
    Bichitrananda Raut, Aakriti Soni, Susanta Kumar Badatya, Satish Saluja, Manoj Modi, Arun Soni
    NeoReviews.2018; 19(9): e542.     CrossRef
Exuberant Smooth Muscle Cells in Fibroadenoma of the Breast: A Case Report.
Ga Eon Kim, Young Kim, Eun Hui Jeong, Jo Heon Kim, Min Ho Park, Ji Shin Lee
Korean J Pathol. 2010;44(4):431-434.
DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.4.431
  • 5,404 View
  • 74 Download
  • 2 Crossref
AbstractAbstract PDF
Smooth muscle cell metaplasia is an extremely rare form of stromal differentiation in fibroadenomas. We describe a case of fibroadenoma with exuberant smooth muscle cells in a 72-year-old woman. The mass was located in the upper central portion of the left breast. It was well circumscribed and its greatest dimension was 3 cm. Histologically, the glandular elements resembled the appearance of fibroadenoma, but the stromal elements were composed of spindle cell bundles with abundant eosinophilic cytoplasm and elongated cigar-shaped nuclei. Neither mitotic activity nor cellular atypia was seen. The stromal cells were immunohistochemically positive for smooth muscle actin, calponin, desmin, and estrogen receptor-beta, but negative for CD34, S-100 protein, p63, CD10, estrogen receptor-alpha, progesterone receptor and cytokeratin. These results proved that the stromal cells showed features of smooth muscle cells.

Citations

Citations to this article as recorded by  
  • Fibroadenomatoid Hyperplasia of the Breast with Prominent Smooth Muscle Component: An Uncommon Histopathological Encounter
    Seetu Palo, Divya Donepudi, Shrinivas Bheemrao Somalwar
    Journal of Mid-life Health.2025; 16(2): 226.     CrossRef
  • Unusual Myoid Differentiation in a Canine Benign Mixed Mammary Tumour
    Barbara Brunetti, Luisa Vera Muscatello, Louis J. DeTolla, Giancarlo Avallone, Isabel Pires
    Case Reports in Veterinary Medicine.2021; 2021: 1.     CrossRef
Original Articles
Oncocytoma and Oncocytic Carcinoma of the Salivary Glands, Single Institute Experience.
Jeong Hyeon Jo, Seung Ho Choi, Jong Lyel Roh, Soon Yuhl Nam, Sang Yoon Kim, Kyung Ja Cho
Korean J Pathol. 2010;44(4):370-375.
DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.4.370
  • 4,494 View
  • 65 Download
  • 2 Crossref
AbstractAbstract PDF
BACKGROUND
Oncocytic neoplasms of the salivary glands are rare and the differential diagnosis between oncocytic carcinomas (OCs) and oncocytomas is difficult. We present 5 cases of oncocytoma and 3 cases of OC of the salivary glands with clinicopathological and immunohistochemical comparisons.
METHODS
Eight cases of oncocytic neoplasms diagnosed at Asan Medical Center between 1998 and 2009 were reviewed for clinical data and histological features. Immunohistochemical staining for epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (Her-2), c-kit, p53, and Ki-67 was done.
RESULTS
Cytological differences between oncocytomas and OCs were not obvious, but unequivocal infiltrative growths were identified in 3 cases, rendering the diagnosis of oncocytic carcinoma. When the remaining cases were classified as oncocytomas, there was no difference in age, size, and clinical symptoms between oncocytomas and OCs. Two of 3 OCs showed strong membranous expression of c-kit, but all oncocytomas were negative. The proportion of p53-positive cells was larger in OCs than oncocytomas. Her-2 or EGFR expression was absent, and Ki-67 labeling indices were less than 1% in all cases.
CONCLUSIONS
An infiltrative growth pattern, strong membranous expression of c-kit, and an increased proportion of p53-positive cells are features that can differentiate OCs from oncocytomas of the salivary glands.

Citations

Citations to this article as recorded by  
  • Clinicopathological Study of Oncocytomas of Head and Neck Region: A Systematic Review
    João Paulo Gonçalves de Paiva, Laura Borges Kirschnick, Daniela Giraldo Roldán, Manoela Domingues Martins, Alan Roger Santos‐Silva, Ciro Dantas Soares, Jacks Jorge
    Journal of Oral Pathology & Medicine.2025; 54(8): 635.     CrossRef
  • Primary oncocytic carcinoma of ectopic salivary gland: a unique case
    E. Touli, A. Manganaris, C. Nikolaidou, I. Karasmanis
    International Journal of Oral and Maxillofacial Surgery.2022; 51(4): 463.     CrossRef
Significance of the Expression of Cathepsins B, H, & L in Colonic Epithelial Neoplasms.
Jae Young Sim, Mi Ja Lee, Keun Hong Kee
Korean J Pathol. 2009;43(5):408-412.
DOI: https://doi.org/10.4132/KoreanJPathol.2009.43.5.408
  • 3,530 View
  • 22 Download
AbstractAbstract PDF
BACKGROUND
Cathepsin is associated with tumorigenesis, tumor invasion and metastasis through its ability to induce degradation of extracellular matrix components.
METHODS
To investigate the correlation between cathepsin expression and tumor progression, invasion depth or nodal metastasis, immunohistochemical staining for cathepsins B, H and L were done on 20 hyperplastic polyps, 48 adenomas, and 67 adenocarcinomas of the colon. Evaluation of the expression of cathepsins B, H and L was based on the percentage of neoplastic cells that stained positive for any given cathepsin.
RESULTS
Cathepsin B expression was significantly higher in adenocarcinomas than adenomas (29.33 vs 5.48%), but was not associated with the degree of differentiation, depth of invasion and nodal status of the tumors. Expression of cathepsins H and L was absent or low in both adenomas and adenocarcinomas. CONCLUSIONS: We suggest that cathepsin B is involved in progression of a subset of colonic adenomas, while cathepsins H and L are not.
Functional Inactivation of pRb Associated with Cyclin D1- and Cyclin-dependent Kinase 4 Overexpression Plays A Key Role in Human Pituitary Tumorigenesis.
Na Hye Myong
Korean J Pathol. 2009;43(1):56-62.
DOI: https://doi.org/10.4132/KoreanJPathol.2009.43.1.56
  • 4,363 View
  • 28 Download
  • 1 Crossref
AbstractAbstract PDF
BACKGROUND
Human pituitary adenoma (PA) is a common intracranial tumor, but the mechanism underlying tumorigenesis has not been established. Functional inactivation of retinoblastoma protein (pRb) following cyclin D1- and cyclin-dependent kinase (CDK) 4-dependent hyperphosphorylation is one of the most important mechanisms in tumor cell proliferation. We evaluated immunohistochemical expressions of cyclin D1, CDK4 and phosphorylated pRb (p-pRb) in 50 PAs to investigate a role for functional inactivation of pRb associated with cyclin D1/CDK4 overexpression in pituitary tumorigenesis and to correlate it with clinicopathologic variables.
METHODS
Fifty human PAs were immunohistochemically stained for cyclin D1, CDK4 and p-pRb (Thr 356). Correlations between their expression and the clinicopathologic characteristics were statistically analyzed.
RESULTS
Cyclin D1 and CDK4 were overexpressed in 56% and 64%, respectively; pRb was hyperphosphorylated in 64%. Forty one cases (82%) showed one or more of these altered expressions. Overexpressions of cyclin D1 and CDK4 were correlated with functional pRb inactivation. Cyclin D1 overexpression was associated with apoplexy and growth hormone production.
CONCLUSIONS
Functional inactivation of pRb associated with the cyclin D1/CDK4 overexpression might play a key role in human pituitary tumorigenesis. CDK4 worked in concert with cyclin D1 to hyperphosphorylate pRb. Pituitary apoplexy appeared to be associated with cyclin D1 overexpression.

Citations

Citations to this article as recorded by  
  • Differential expression of cyclin D1 in human pituitary tumors: relation to MIB-1 and p27/Kip1 labeling indices
    Iman H. Hewedi, Wesam M. Osman, Manal M. El Mahdy
    Journal of the Egyptian National Cancer Institute.2011; 23(4): 171.     CrossRef
Cytologic Features of Folliculars Adenoma and Follicular Carcinoma of the Thyroid: A Study on the Likelihood of Cytologic Diagnosis by Fine Needle Aspiration Cytology.
Hee Dae Park, Woon Sun Park, Sun Hee Kim, Seock Hyun Choi, Young Hye Cho, Sung Hee Kang, Kyung Bun Lee, Dong Hoon Kim, Seoung Wan Chae, Jin Hee Shon
J Pathol Transl Med. 2008;19(2):152-159.
DOI: https://doi.org/10.3338/kjc.2008.19.2.152
  • 12,612 View
  • 218 Download
  • 2 Crossref
AbstractAbstract PDF
Fine-needle aspiration cytology (FNAC) cannot differentiate follicular adenoma from follicular carcinoma since this distinction can only be based on the presence of capsular or vascular invasion, and this cannot be detected on a cytologic smear. The goal of this study was to define the diagnostic cytologic findings of follicular neoplasm and the possibility of diagnosing follicular neoplasm by performing FNAC. The cases of histologically diagnosed follicular adenoma and follicular carcinoma on the thyroidectomy specimens were retrieved. Among them, the cases with preoperative FNAC that was done within 3 months of the operation were finally selected. Then we reviewed the FNAC and histologic slides of 19 cases: 9 follicular adenomas and 10 follicular carcinomas. Our results suggest that for cases of follicular neoplasm, the aspirates show high or abundant cellularity, frequent follicle formation and occasional cellular atypism of the follicular cells. However, the atypism is more pronounced and more frequently noticed in the cases of follicular carcinoma, which reveals more higher anisocytosis (7/10, 70%), nuclear pleomorphism (9/10, 90%), coarse clumping of chromatin (8/10, 80%) and cellular overlapping (8/10, 80%).

Citations

Citations to this article as recorded by  
  • Practical and challenging issue in thyroid cytopathology
    Qianqian Zhang, Belen Padial Urtueta, Elisabetta Merenda, Gabriele Rotondaro, Noemi Morelli, Alessia Piermattei, Patrizia Straccia, Federica Cianfrini, Angela Feraco, Alessia Granitto, Antonino Mule, Esther Diana Rossi
    Human Pathology.2025; : 106019.     CrossRef
  • Fine Needle Aspiration Cytology of Thyroid Follicular Neoplasm: Cytohistologic Correlation and Accuracy
    Changyoung Yoo, Hyun Joo Choi, Soyoung Im, Ji Han Jung, Kiouk Min, Chang Suk Kang, Young-Jin Suh
    Korean Journal of Pathology.2013; 47(1): 61.     CrossRef
Case Reports
Cytologic Features of Epithelial-Myoepithelial Carcinoma Occurring in External Auditory Canal: A Case Report.
Ho chang Lee, Hyung Geun Song, Young Seok Choi, Ok Jun Lee
J Pathol Transl Med. 2008;19(1):52-56.
DOI: https://doi.org/10.3338/kjc.2008.19.1.52
  • 2,790 View
  • 16 Download
AbstractAbstract PDF
Epithelial-myoepithelial carcinoma (EMC) is a low grade malignant neoplasm that commonly occurs in the parotid gland. Recently, we investigated a case of EMC that occurred in the external auditory canal (EAC) in a 35-year-old male, and this tumor was initially diagnosed as pleomorphic adenoma. The difficulty associated with diagnosing EMC by aspiration cytology arises from both the rare incidence of this tumor and the overlapping spectrum of cytological features found in various salivary gland tumors, such as pleomorphic adenoma, basal cell adenoma and adenoid cystic carcinoma.
Touch Imprint Cytology of Adenomatoid Tumor of the Tunica Albuginea: A Case Report.
Jong Im Lee
J Pathol Transl Med. 2008;19(1):47-51.
DOI: https://doi.org/10.3338/kjc.2008.19.1.47
  • 2,936 View
  • 14 Download
  • 2 Crossref
AbstractAbstract PDF
Adenomatoid tumor is a benign neoplasm of a mesothelial origin, and it usually occurs in the reproductive organs, especially in the epididymis. The author experienced a case of adenomatoid tumor involving the tunica albuginea and testicular parenchyme without any evidence of epididymis involvement. The patient was a 36-year-old man with a painless scrotal mass that he had experienced for 2 months, and this mimicked testicular neoplasia, including metastatic carcinoma, or other benign lesions. The imprint cytology of the tumor showed a hypocellular smear with mainly arranged cells in cohesive monolayered clusters along with occasional singly dispersed cells and naked nuclei in a clean background. The cellular clusters formed vague glandular and cord-like structures. The tumor cells were large polygonal to columnar cells with a relatively monomorphic appearance. The nuclei were oval to round shape and they showed vesicular, fine chromatin and inconspicuous nucleoli. The cytoplasm was moderate to abundant, and it contained fine vacuoles in some tumor cells. Mitoses and cellular pleomorphism were not present. Awareness of the cytologic finding of this lesion is necessary to screen or differentiate a testicular or paratesticular mass before and/or during surgery because the cytology may be useful as a diagnostic tool. Pathologists should be aware of the cytologic features of common lesions in this anatomic region so as to avoid performing aggressive and unnecessary surgical procedures.

Citations

Citations to this article as recorded by  
  • Adenomatoid Tumor of the Tunica Albuginea in a Boy: A Case Report and Literature Review
    Kaimin Guo, Runhui Tian, Lingyun Liu, Congqi Du, Fubiao Li, Hongliang Wang
    Case Reports in Urology.2015; 2015: 1.     CrossRef
  • Aspiration cytology of adenomatoid tumor of epididymis: An important diagnostic tool
    S. Gupta, S. Garg, R. Agarwal, R. Sen
    Journal of Surgical Case Reports.2012; 2012(4): 11.     CrossRef
Cytologic Features of Adenoma Malignum of the Uterine Cervix: A Case Report.
Hyun Joo Choi, Young Shin Kim, Kyo Young Lee, Chang Suk Kang, Sang In Shim
J Pathol Transl Med. 1998;9(2):201-206.
  • 2,285 View
  • 22 Download
AbstractAbstract PDF
Adenoma malignum is an extremely well-differentiated variant of cervical adeno carcinoma in which the cells composing the tumor lack the typical cytological features of malignancy. The prognosis of this rare tumor is poor in spite of high degree of differentiation. The cytologic characteristics are extremely bland, so frequently make a confusion of adenoma malignum with endocervical glandular hyperplasia. We report a case of adenoma malignum in a 36-year-old woman who complained of mucoid vaginal discharge and vaginal bleeding. The cervicovaginal smear showed endocervical cells exhibiting a spectrum of atypical changes. The cells were arranged in multilayered strips and monolayered sheets. Individual cells ranged from cuboidal to columnar; typically the columnar cells had abundant lacy or vacuolated cytoplasm. The smear showed the majority of only atypical cells and small numbers of frankly malignant cells.
Original Article
Cystandenoma and Primary Cystadenocarcinoma of the Liver.
Kyoung Ho Kim, Chan Il Park
Korean J Pathol. 1989;23(2):263-268.
  • 2,280 View
  • 10 Download
AbstractAbstract PDF
Primary cystic neoplasia of the liver is rare. We report a cystadenoma with mesenchymal stroma (CMS) and a cystadenocarcinoma, and make a review of literature with particular reference to their histogenesis. The CMS has many similarities to the ovarian mucinous cystadenoma; occurring almost exlusively in female, being lined by mucus-secreting epithelial cells, and containing dense ovarian-like stroma. These features suggest that CMS may arise from the ectopic ovarian tissue within the liver. Cystadenocarcinoma may have its origin in CMS or cystadenoma without mesenchymal stroma of CMS. Cholangiocarcinoma arising from the congenital hepatic cysts can be differentiated only when it contains benign epithelia.
Case Reports
Juvenile Cellular Adenofibroma of Breast: A case report.
Je G Chi, Yeon Lim Suh
Korean J Pathol. 1989;23(2):269-272.
  • 1,952 View
  • 16 Download
AbstractAbstract PDF
Juvenile cellular adenofibroma of the breast is a unique neoplasm of the breast that should be differentiated from other important benign and malignant lesions of the juvenile breasts. We report a case with it's characteristic clinical, gross and histological features. The tumor was in the right breast with the size of 20 cm in maximum extent. This patient was also associated with hemihypertrophy of the right side. Microscopically the masses were characterized by prominent stromal cellularity associated with pericanalicular duct proliferation.
Acinar Cell Cystadenoma of the Pancreas: Report of a Case with Metaplastic Ossification.
Baek Hee Kim, Seog Yun Park, Bomi Kim, Gyeong Hoon Kang
Korean J Pathol. 2007;41(3):203-206.
  • 2,208 View
  • 27 Download
AbstractAbstract PDF
Acinar cell cystadenoma (ACA) is a very rare cystic lesion of the pancreas. The lining epithelium of ACA is morphologically identical to acinar cells of the pancreas. It is uncertain whether ACA is a benign neoplasm or cystic transformation of acinar glands but it is worthy to consider ACA in the differential diagnosis of other cystic neoplasms of the pancreas. We report here a 25-year old-woman who was operated on for a cystic mass of the pancreas. Grossly, a multilocular cystic mass containing clear serous fluid was observed. There was no communication between the cysts and the pancreatic ducts. Microscopically, cysts of various size were lined by columnar, cuboidal or flattened epithelial cells with a few foci of pseudostratification. The cells had granular apical cytoplasm and basally located nuclei with minimal atypia, the same as normal acinar cells. Metaplastic ossification was noted in the stroma. Immunohistochemically, the lining epithelium was positive for cytokeratin 7, antitrypsin and antichymotrypsin.
Giant Multilocular Cystadenoma of the Prostate: A Case Report.
Chang Ohk Sung, Jinwon Seo, Sang Yong Song
Korean J Pathol. 2004;38(2):106-108.
  • 2,110 View
  • 30 Download
AbstractAbstract PDF
Large multilocular cysts and cystic neoplasms of the prostate are very rare. A healthy 52-year-old man presented with acute urinary retension. Physical examination revealed a large abdominal mass. Pelvic MRI showed a 15x10x9 cm, lobulated, and multiseptated cystic mass in the pelvic cavity. Exploration laparotomy revealed a large cytic mass that compressd and displaced the urinary bladder antero-laterally, and adhered to the prostate and the sigmoid colon. Macroscopically, the mass was grayish white colored, multilocular cysts containing reddish-brown serous fluid. Microscopically, the tumor was composed of glands and cysts lined by the prostatic-type epithelium in the fibrous stroma. The prostatic nature of the lesion was confirmed by the lining epithelium expressing prostate-specific antigen.
Retroperitoneal Mucinous Tumor: Report of two Cases.
Eun Kyung Kim, Seong Ran Hong, Hy Sook Kim, Young Hyeh Ko, Jung Dal Lee
Korean J Pathol. 1992;26(6):632-634.
  • 1,996 View
  • 15 Download
AbstractAbstract PDF
Primary retroperitoneal mucinous tumor is very rare. In the worldwide literature, only 14 cases have been reported. Herein, we report two cases of retroperitoneal mucinous tumor found at laparotomy. The patients were females, aged 24 and 21 years, respectively. They had bilateral normal ovaries. Histologically, one was mucinous cystadenoma and the other showed borderline histology. The connective tissue wall resembling ovarian stroma was noted in one case. The pathogenesis was discussed.
Mucous Gland Adenoma Presenting as a Peripheral Lung Mass: A Brief Case Report.
Ji Eun Kwon, Gou Young Kim, Joungho Han, Tae Sung Kim, Kwanmien Kim
Korean J Pathol. 2004;38(2):126-128.
  • 2,219 View
  • 17 Download
AbstractAbstract PDF
Mucous gland adenoma (MGA) of the lung is an uncommon, benign tumor that histologically resembles the mucus-secreting component of the tracheobronchial gland. The majority arises within the main, lobar or segmental bronchi. MGA presenting as a peripheral lung mass is extremely rare. We herein report a case of MGA that uniquely arose from the peripheral territory of the superior segmental bronchus of the left lower lobe in a 73-year-old male. Chest computed tomography showed a 13 mm-sized, subpleural nodule, which was easily enucleated by video-assisted thoracotomy. The mass was round and gray-tan in color with mucoid material. The tumor was composed of cysts, tubules, and glands lined by bland columnar, cuboidal or flattened, mucus secreting cells.
Original Article
Cytologic Analysis of Fibroadenomas of Breast Overdiagnosed as High Risk Group in Fine Needle Aspiration Cytology .
Sung Hye Park, Gil Sook Yoon, Misun Choi, Shin Kwang Khang
J Pathol Transl Med. 1999;10(2):127-127.
  • 2,618 View
  • 29 Download
AbstractAbstract PDF
Among total 108 cases of biopsy-proven fibroadenomas of the breast, which obtained from the files of the Asan Medical Center during one year period from October 1998 to September 1999, 23 cases cytologically diagnosed as high risk group were reviewed to retrieve the mis-leading factors. Initial cytologic diagnoses of 23 cases were proliferative breast lesion with atypia(high risk) in 21 cases(91.3%) and papillary neoplasm in 2 cases(8.7%). When we reanalysed 23 cases by Masood scoring system, they were classified as one non-proliferative breast lesion(4.3%), 16 proliferative breast lesions without atypia (69.6%), and 6 proliferative breast lesions with atypia(26.1%). None were subject to the category of carcinoma. Cytologic features leading to the overdiagnosis of high grade epithelial lesions were as follows; cellular dissociation without nuclear atypia, nuclear pleomorphism, anisonucleosis, and occasional macronucleoli without nuclear enlargement, lack of myxoid stroma, and few naked stromal cells. To avoid cytologic overdiagnosis of fibroadenoma, mild to moderate nuclear pleomorphism without nuclear enlargement, and cellular dissociation without nuclear atypia should not be regarded as criteria of high risk group.
Case Reports
Trichoadenoma: Report of a case.
Youn Soo Lee, Mi Kyung Lee, Seok Jin Gang, Byoung Kee Kim, Sun Moo Kim
Korean J Pathol. 1993;27(1):75-77.
  • 2,150 View
  • 26 Download
AbstractAbstract PDF
The clinical and pathological features of trichoadenoma are presented. Trichoadenoma is very rare, and as far as we know, no report on the trichoadenoma has been published in korea literature. We experienced a case of trichoadenoma occured in a 29 year-old male, who had a 0.9x0.7x0.4cm sized and slowly growing mass in the right buttock. The histopathological findings and histogenesis of trichoadenoma were discussed and a brief review of the literature was made.
Imprint Cytologic Features of Fibroadenoma of the Breast with Extensive Infarction: A Case Report .
Suk Jin Choi, Jong Im Lee, Jung Ran Kim, Tae Jung Jang, Ki Kwon Kim, Dong Hoon Kim, Byoung Ook Jeoung
J Pathol Transl Med. 1999;10(2):169-174.
  • 2,103 View
  • 25 Download
AbstractAbstract PDF
Spontaneous Infarction of fibroadenoma of the breast is very uncommon and may lead to difficulties in clinical and pathological diagnosis. Most reported cases occured in young women during pregnancy or lactation. This report describes imprint cytologic features of an infarcted fibroadenoma in a 19-year-old young woman without evidence of pregnancy. The smears revealed many individually scattered degenerated or necrotic epithelial or spindle stromal cells and naked nuclei on dirty necrotic background. A few sheets of cohesive uniform epithelial cells and a few fragments of stromal cells were also present. Most of the epithelial cells had pyknotic and hyperchromatic nuclei, however, cellular atypism such as pleomorphism, prominent nucleoli or mitosis were not present. Though the necrotic ductular and glandular outline of this case may bear a superficial resemblance to adenocarcinoma, obvious cytologic atypia or mitosis, even in the necrotic areas, were not present.
Fine Needle Aspiration Cytology of the Hyalinizing Trabecular Adenoma of the Thyroid Gland: A Case Report .
Seong Ho Kim, Seung Sam Paik, Moon Hyang Park
J Pathol Transl Med. 1999;10(2):175-178.
  • 1,853 View
  • 12 Download
AbstractAbstract PDF
Hyalinizing trabecular adenoma is an uncommon benign thyroid tumor that is recently described in the literature. This tumor is easily confused with medullary carcinoma on surgical specimens and with papillay carcinoma on cytologic specimens. Herein we report the cytologic characteristics of a case of histologically proven hyalinizing trabecular adenoma of the thyroid gland. Cytologically, the aspirate showed trabecular or individually dispersed polygonal cells with finely stippled chromatin pattern, nuclear grooves, and eosinophilic nuclear pseudoinclusions. No colloid materials were noted in the background.
Original Article
The Significance of Nesidiodysplasia of the Pancreas.
Soo Im Choi, Woo Hee Jeong, Chan Il Park
Korean J Pathol. 1990;24(1):10-15.
  • 1,905 View
  • 12 Download
AbstractAbstract PDF
To elucidate the significance of the nesidiodysplasia of pancreas, histological re-evaluation and immunohistochemical studies for insulin, glucagon and somatostatin were done on 16 consecutive cases (5 premature babies, 2 stillborns, 5 infants and 3 adults) in which paraffin blocks of the pancreas were available. Only one infant was hypoglycemic. All 16 pancreases showed changes of nesidiodysplasia which appeared immunohistochemically to have isulin, glucagon and /or somatostatin. The histologic patterns of nesidiodysplasia included ductoendocrine proliferation, endocrine cell dysplasia, adenomatosis, septal islet, islket cell hypertrophy and islet hypertrophy. All the patterns of nesidiodysplasia except for the adenomatosis were seen in premature babies, infants, stillborns and adults with or without hypoglycemia. The adenomatosis was found only in the hypoglycemic infant. The result suggests that all patterns of nesidiodysplasia of other than the adenomatosis does not imply the pathologic basis of hypoglycemia.

J Pathol Transl Med : Journal of Pathology and Translational Medicine
TOP