Skip Navigation
Skip to contents

J Pathol Transl Med : Journal of Pathology and Translational Medicine

OPEN ACCESS
SEARCH
Search

Search

Page Path
HOME > Search
9 "Seung-Ho Choi"
Filter
Filter
Article category
Keywords
Publication year
Authors
Original Articles
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
  • 1,419 View
  • 94 Download
  • 1 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  
  • 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
Primary squamous cell carcinoma of the salivary gland: immunohistochemical analysis and comparison with metastatic squamous cell carcinoma
Uiree Jo, Joon Seon Song, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Kyung-Ja Cho
J Pathol Transl Med. 2020;54(6):489-496.   Published online August 31, 2020
DOI: https://doi.org/10.4132/jptm.2020.07.19
  • 5,209 View
  • 156 Download
  • 11 Web of Science
  • 13 Crossref
AbstractAbstract PDFSupplementary Material
Background
Primary squamous cell carcinoma (SCC) of the salivary gland is a rare disease, and distinguishing primary SCC from metastatic SCC is difficult. This study investigated the histological and immunohistochemical differences between primary and metastatic salivary gland SCC to improve the accuracy of diagnosis and to explore the pathogenesis of this disease.
Methods
Data of 16 patients who underwent surgery for SCC of salivary glands between 2000 and 2018 at Asan Medical Center were retrieved. Eight patients had a history of SCC at other sites, and eight patients had only salivary gland SCC. Immunostaining for p16, p53, androgen receptor (AR), gross cystic disease fluid protein 15 (GCDFP-15), and c-erbB2, as well as mucicarmine staining, were compared between the two groups.
Results
Most tumors were located in the center of the salivary glands with extraparenchymal extension. The histology of primary SCC of the salivary gland was consistent with moderately differentiated SCC with extensive desmoplastic reaction and peritumoral inflammation. Involvement of the salivary gland ducts and transition into the ductal epithelium were observed in two cases. Metastatic SCC resembled the primary tumor histologically and was associated with central necrosis. Both groups exhibited negative mucin staining. Two, one, and one primary SCC case exhibited AR, GCDFP-15, and c-erbB2 positivity, respectively.
Conclusions
A subset of primary SCCs originated in salivary ducts or was related to salivary duct carcinoma. Distinguishing primary from metastatic SCC of the salivary gland is difficult using histologic features and immunoprofiles. A comprehensive review of the medical history is essential.

Citations

Citations to this article as recorded by  
  • Primary salivary gland squamous cell carcinoma with sialolithiasis in the submandibular gland: A case report and literature review
    Sawako Ono, Katsutoshi Hirose, Yuji Hirata, Marie Yamada, Satoko Nakamura, Hidetaka Yamamoto
    Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2024;[Epub]     CrossRef
  • A case of primary squamous cell carcinoma of the parotid gland and review of the literature
    Jingli Zhao, Xinrong Nan, Chuhuan Zhou, Nan Jiang, Liangliang Tian
    Journal of Case Reports and Images in Oncology.2024; 10(1): 7.     CrossRef
  • Metastatic cutaneous squamous cell carcinoma accounts for nearly all squamous cell carcinomas of the parotid gland
    Patrick J. Bradley, Göran Stenman, Lester D. R. Thompson, Alena Skálová, Roderick H. W. Simpson, Pieter J. Slootweg, Alessandro Franchi, Nina Zidar, Alfons Nadal, Henrik Hellquist, Michelle D. Williams, Ilmo Leivo, Abbas Agaimy, Alfio Ferlito
    Virchows Archiv.2024;[Epub]     CrossRef
  • Salivary gland fine needle aspiration: a focus on diagnostic challenges and tips for achieving an accurate diagnosis
    Carla Saoud, Hansen Lam, Sandra I. Sanchez, Zahra Maleki
    Diagnostic Histopathology.2023; 29(8): 357.     CrossRef
  • Salivary gland pathologies: evolution in classification and association with unique genetic alterations
    Michał Żurek, Łukasz Fus, Kazimierz Niemczyk, Anna Rzepakowska
    European Archives of Oto-Rhino-Laryngology.2023; 280(11): 4739.     CrossRef
  • A retrospective study of nonneoplastic and neoplastic disorders of the salivary glands
    Sorin Vamesu, Oana Andreea Ursica, Ana Maria Gurita, Raluca Ioana Voda, Mariana Deacu, Mariana Aschie, Madalina Bosoteanu, Georgeta Camelia Cozaru, Anca Florentina Mitroi, Cristian Ionut Orasanu
    Medicine.2023; 102(42): e35751.     CrossRef
  • Pembrolizumab as a first line therapy in a patient with extensive mucoepidermoid salivary gland carcinoma. A complete clinical, radiological and pathological response. A very specific case
    Raed Farhat, Noam Asna, Yaniv Avraham, Ashraf Khater, Majd Asakla, Alaa Safia, Sergio Szvalb, Nidal Elkhatib, Shlomo Merchavy
    Discover Oncology.2022;[Epub]     CrossRef
  • Morphologic CT and MRI features of primary parotid squamous cell carcinoma and its predictive factors for differential diagnosis with mucoepidermoid carcinoma
    Xiaohua Ban, Huijun Hu, Yue Li, Lingjie Yang, Yu Wang, Rong Zhang, Chuanmiao Xie, Cuiping Zhou, Xiaohui Duan
    Insights into Imaging.2022;[Epub]     CrossRef
  • A Rare Case of Primary Squamous Cell Carcinoma of the Submandibular Salivary Gland: Brief Overview of Diagnostic Ambiguity and Treatment Challenges
    Pawan Hingnikar, Anendd Jadhav, Nitin D Bhola
    Cureus.2022;[Epub]     CrossRef
  • Necrotizing Sialometaplasia of the Hard Palate: Diagnosis and Treatment
    Sangeun Lee, Yun Sung Lim, Kyuho Lee, Bo Hae Kim
    Journal of Clinical Otolaryngology Head and Neck Surgery.2022; 33(4): 236.     CrossRef
  • Parotid Salivary Duct Carcinoma With a Prominent Squamous Component: Immunohistochemical Profile, Diagnostic Pitfalls, and Therapeutic Implications
    Naomi Hardy, Joshua Thompson, Ranee Mehra, Cinthia B. Drachenberg, Kyle Hatten, John C. Papadimitriou
    International Journal of Surgical Pathology.2021; 29(7): 726.     CrossRef
  • Intrasalivary Thymic Carcinoma: A Case Report and Literature Review
    Michał Kunc, Alexandra Kamieniecki, Grzegorz Walczak, Tomasz Nowicki, Bartosz Wasąg, Bogusław Mikaszewski, Dominik Stodulski, Wojciech Biernat
    Head and Neck Pathology.2021; 16(3): 857.     CrossRef
  • Cancer Stem Cell Markers in Squamous Cell Carcinomas of the Salivary Glands
    Mattis Bertlich, Julia Kitz, Marie Kruizenga, Jennifer Lee Spiegel, Martin Canis, Friedrich Ihler, Frank Haubner, Bernhard G. Weiss, Mark Jakob
    Oncology.2021; 99(6): 402.     CrossRef
Comparison of Squamous Cell Carcinoma of the Tongue between Young and Old Patients
Gyuheon Choi, Joon Seon Song, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Jong-Lyel Roh, Bu-Kyu Lee, Kyung-Ja Cho
J Pathol Transl Med. 2019;53(6):369-377.   Published online October 11, 2019
DOI: https://doi.org/10.4132/jptm.2019.09.16
  • 5,694 View
  • 177 Download
  • 6 Web of Science
  • 9 Crossref
AbstractAbstract PDFSupplementary Material
Background
The worldwide incidence of squamous cell carcinoma of the tongue (SCCOT) in young patients has been increasing. We investigated clinicopathologic features of this unique population and compared them with those of SCCOT in the elderly to delineate its pathogenesis.
Methods
We compared clinicopathological parameters between patients under and over 45 years old. Immunohistochemical assays of estrogen receptor, progesterone receptor, androgen receptor, p53, p16, mdm2, cyclin D1, and glutathione S-transferase P1 were also compared between them.
Results
Among 189 cases, 51 patients (27.0%) were under 45 years of age. A higher proportion of women was seen in the young group, but was not statistically significant. Smoking and drinking behaviors between age groups were similar. Histopathological and immunohistochemical analysis showed no significant difference by age and sex other than higher histologic grades observed in young patients.
Conclusions
SCCOT in young adults has similar clinicopathological features to that in the elderly, suggesting that both progress via similar pathogenetic pathways.

Citations

Citations to this article as recorded by  
  • High Failure Rates in Young Nonsmoker Nondrinkers With Squamous Cell Carcinoma of the Oral Tongue
    Brianna M. Jones, Dillan F. Villavisanis, Eric J. Lehrer, Daniel R. Dickstein, Kunal K. Sindhu, Krzysztof J. Misiukiewicz, Marshall Posner, Jerry T. Liu, Vishal Gupta, Sonam Sharma, Scott A. Roof, Marita Teng, Eric M. Genden, Richard L. Bakst
    The Laryngoscope.2023; 133(5): 1110.     CrossRef
  • Characteristics of oral squamous cell carcinoma focusing on cases unaffected by smoking and drinking: A multicenter retrospective study
    Hiroyuki Harada, Masahiro Kikuchi, Ryo Asato, Kiyomi Hamaguchi, Hisanobu Tamaki, Masanobu Mizuta, Ryusuke Hori, Tsuyoshi Kojima, Keigo Honda, Takashi Tsujimura, Yohei Kumabe, Kazuyuki Ichimaru, Yoshiharu Kitani, Koji Ushiro, Morimasa Kitamura, Shogo Shino
    Head & Neck.2023; 45(7): 1812.     CrossRef
  • Genetic characteristics of advanced oral tongue squamous cell carcinoma in young patients
    Sehui Kim, Chung Lee, Hyangmi Kim, Sun Och Yoon
    Oral Oncology.2023; 144: 106466.     CrossRef
  • Oral Squamous Cell Carcinoma Frequency in Young Patients from Referral Centers Around the World
    Rafael Ferreira e Costa, Marina Luiza Baião Leão, Maria Sissa Pereira Sant’Ana, Ricardo Alves Mesquita, Ricardo Santiago Gomez, Alan Roger Santos-Silva, Syed Ali Khurram, Artysha Tailor, Ciska-Mari Schouwstra, Liam Robinson, Willie F. P. van Heerden, Rami
    Head and Neck Pathology.2022; 16(3): 755.     CrossRef
  • Early-onset oral cancer as a clinical entity: aetiology and pathogenesis
    E.S. Kolegova, M.R. Patysheva, I.V. Larionova, I.K. Fedorova, D.E. Kulbakin, E.L. Choinzonov, E.V. Denisov
    International Journal of Oral and Maxillofacial Surgery.2022; 51(12): 1497.     CrossRef
  • The effect of age on the clinicopathological features of oral squamous cell carcinoma
    Alaa S Saeed, Bashar H Abdullah
    Journal of Baghdad College of Dentistry.2022; 34(1): 25.     CrossRef
  • Survival Outcomes in Oral Tongue Cancer: A Mono-Institutional Experience Focusing on Age
    Mohssen Ansarin, Rita De Berardinis, Federica Corso, Gioacchino Giugliano, Roberto Bruschini, Luigi De Benedetto, Stefano Zorzi, Fausto Maffini, Fabio Sovardi, Carolina Pigni, Donatella Scaglione, Daniela Alterio, Maria Cossu Rocca, Susanna Chiocca, Sara
    Frontiers in Oncology.2021;[Epub]     CrossRef
  • A meta-analysis of oral squamous cell carcinoma in young adults with a comparison to the older group patients (2014–2019)
    Khadijah Mohideen, C Krithika, Nadeem Jeddy, Thayumanavan Balakrishnan, R Bharathi, SLeena Sankari
    Contemporary Clinical Dentistry.2021; 12(3): 213.     CrossRef
  • Modern perspectives of oral squamous cell carcinoma
    A.A. Ivina
    Arkhiv patologii.2020; 82(3): 55.     CrossRef
Basaloid Squamous Cell Carcinoma of the Head and Neck: Subclassification into Basal, Ductal, and Mixed Subtypes Based on Comparison of Clinico-pathologic Features and Expression of p53, Cyclin D1, Epidermal Growth Factor Receptor, p16, and Human Papillomavirus
Kyung-Ja Cho, Se Un Jeong, Sung Bae Kim, Sang-wook Lee, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim
J Pathol Transl Med. 2017;51(4):374-380.   Published online June 8, 2017
DOI: https://doi.org/10.4132/jptm.2017.03.03
  • 13,737 View
  • 378 Download
  • 9 Web of Science
  • 11 Crossref
AbstractAbstract PDF
Background
Basaloid squamous cell carcinoma (BSCC) is a rare variant of squamous cell carcinoma with distinct pathologic characteristics. The histogenesis of BSCC is not fully understood, and the cancer has been suggested to originate from a totipotent primitive cell in the basal cell layer of the surface epithelium or in the proximal duct of secretory glands.
Methods
Twenty-six cases of head and neck BSCC from Asan Medical Center, Seoul, Korea, reported during a 14-year-period were subclassified into basal, ductal, and mixed subtypes according to the expression of basal (cytokeratin [CK] 5/6, p63) or ductal markers (CK7, CK8/18). The cases were also subject to immunohistochemical study for CK19, p53, cyclin D1, epidermal growth factor receptor (EGFR), and p16 and to in situ hybridization for human papillomavirus (HPV), and the results were clinico-pathologically compared.
Results
Mixed subtype (12 cases) was the most common, and these cases showed hypopharyngeal predilection, older age, and higher expression of CK19, p53, and EGFR than other subtypes. The basal subtype (nine cases) showed frequent comedo-necrosis and high expression of cyclin D1. The ductal subtype (five cases) showed the lowest expression of p53, cyclin D1, and EGFR. A small number of p16- and/or HPV-positive cases were not restricted to one subtype. BSCC was the cause of death in 19 patients, and the average follow-up period for all patients was 79.5 months. Overall survival among the three subtypes was not significantly different.
Conclusions
The results of this study suggest a heterogeneous pathogenesis of head and neck BSCC. Each subtype showed variable histology and immunoprofiles, although the clinical implication of heterogeneity was not determined in this study.

Citations

Citations to this article as recorded by  
  • HPV-associated oropharyngeal cancer: epidemiology, molecular biology and clinical management
    Matt Lechner, Jacklyn Liu, Liam Masterson, Tim R. Fenton
    Nature Reviews Clinical Oncology.2022; 19(5): 306.     CrossRef
  • Neoadjuvant treatment combined with planned endoscopic surgery in locally advanced sphenoid sinus basaloid squamous cell carcinoma
    Yinghong Zhang, Suqing Tian, Yali Du, Qiang Zuo, Li Zhu, Furong Ma
    Medicine: Case Reports and Study Protocols.2022; 3(6): e0044.     CrossRef
  • Cetuximab and paclitaxel combination therapy for recurrent basaloid squamous cell carcinoma in the ethmoid sinus
    Satoshi Koyama, Kazunori Fujiwara, Tsuyoshi Morisaki, Taihei Fujii, Yosuke Nakamura, Takahiro Fukuhara, Hiromi Takeuchi
    Auris Nasus Larynx.2021; 48(6): 1189.     CrossRef
  • Constitutive Hedgehog/GLI2 signaling drives extracutaneous basaloid squamous cell carcinoma development and bone remodeling
    Marina Grachtchouk, Jianhong Liu, Mark E Hutchin, Paul W Harms, Dafydd Thomas, Lebing Wei, Aiqin Wang, Donelle Cummings, Lori Lowe, Jonathan Garlick, James Sciubba, Arul M Chinnaiyan, Monique E Verhaegen, Andrzej A Dlugosz
    Carcinogenesis.2021; 42(8): 1100.     CrossRef
  • Conjunctival ‘mucoepidermoid carcinoma’ revisited: a revision of terminology, based on morphologic, immunohistochemical and molecular findings of 14 cases, and the 2018 WHO Classification of Tumours of the Eye
    Hardeep S. Mudhar, Tatyana Milman, Paul J.L. Zhang, Carol L. Shields, Ralph C. Eagle, Sara E. Lally, Jerry A. Shields, Sachin M. Salvi, Paul A. Rundle, Jennifer Tan, Ian G. Rennie
    Modern Pathology.2020; 33(7): 1242.     CrossRef
  • Basaloid squamous cell carcinoma with adenoid cystic‐like features of the head and neck region: A report of two cases
    Kimihide Kusafuka, Haruna Yagi, Satoshi Baba, Hiroshi Inagaki, Chinatsu Tsuchiya, Kazuki Hirata, Aya Muramatsu, Makoto Suzuki, Kazumori Arai, Tadashi Terada
    Pathology International.2020; 70(10): 767.     CrossRef
  • Association study of cell cycle proteins and human papillomavirus in laryngeal cancer in Chinese population
    Lifang Cui, Congling Qu, Honggang Liu
    Clinical Otolaryngology.2019; 44(3): 323.     CrossRef
  • Liver metastatic basaloid squamous cell carcinoma with negative expression of pancytokeratin: a case report and literature review
    Linxiu Liu, Xuemin Xue, Liyan Xue
    Diagnostic Pathology.2019;[Epub]     CrossRef
  • Basaloid Squamous Cell Carcinoma at the Floor of the Mouth and Mandible: A Case Report
    Jun-Sang Lee, Uk-Kyu Kim, Dae-Seok Hwang, Jun-Ho Lee, Hong-Seok Choi, Na-Rae Choi, Mi Heon Ryu, Gyoo Cheon Kim
    The Korean Journal of Oral and Maxillofacial Pathology.2019; 43(5): 197.     CrossRef
  • p53 and p16 expression in oral cavity squamous cell and basaloid squamous cell carcinoma
    Allisson Filipe Lopes Martins, Carlos Henrique Pereira, Marília Oliveira Morais, Paulo Otávio Carmo Souza, Lucas Borges Fleury Fernandes, Aline Carvalho Batista, Elismauro Francisco Mendonça
    Oral Cancer.2018; 2(1-2): 7.     CrossRef
  • Expression and role of EGFR, cyclin�D1 and KRAS in laryngocarcinoma tissues
    Xinsheng Lin, Guofeng Wen, Shuangle Wang, Hangui Lu, Chuangwei Li, Xin Wang
    Experimental and Therapeutic Medicine.2018;[Epub]     CrossRef
Accuracy of Core Needle Biopsy Versus Fine Needle Aspiration Cytology for Diagnosing Salivary Gland Tumors
In Hye Song, Joon Seon Song, Chang Ohk Sung, Jong-Lyel Roh, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Jeong Hyun Lee, Jung Hwan Baek, Kyung-Ja Cho
J Pathol Transl Med. 2015;49(2):136-143.   Published online March 12, 2015
DOI: https://doi.org/10.4132/jptm.2015.01.03
  • 10,599 View
  • 185 Download
  • 66 Web of Science
  • 63 Crossref
AbstractAbstract PDF
Background
Core needle biopsy is a relatively new technique used to diagnose salivary gland lesions, and its role in comparison with fine needle aspiration cytology needs to be refined. Methods: We compared the results of 228 ultrasound-guided core needle biopsy and 371 fine needle aspiration procedures performed on major salivary gland tumors with their postoperative histological diagnoses. Results: Core needle biopsy resulted in significantly higher sensitivity and more accurate tumor subtyping, especially for malignant tumors, than fine needle aspiration. No patient developed major complications after core needle biopsy. Conclusions: We recommend ultrasoundguided core needle biopsy as the primary diagnostic tool for the preoperative evaluation of patients with salivary gland lesions, especially when malignancy is suspected.

Citations

Citations to this article as recorded by  
  • Giant Pleomorphic Adenoma of Submandibular Gland
    Harendra Kumar, Qazi Saquib Rizwan, Mayank Gupta, Tarun Kumar
    Indian Journal of Otolaryngology and Head & Neck Surgery.2024; 76(1): 1361.     CrossRef
  • CT-guided core needle biopsies of head and neck tumors: a comprehensive monocenter analysis of safety and outcomes
    Thomas Joseph Vogl, Heinrich Johannes Ketelsen, Scherwin Mahmoudi, Jan-Erik Scholtz, Vitali Koch, Leon David Grünewald, Peter Wild, Timo Stoever, Simon Bernatz
    European Radiology.2024;[Epub]     CrossRef
  • Indications for Submandibulectomy Within a 20-Year Period
    Amir Bolooki, Anna Stenzl, Christopher Weusthof, Benedikt Hofauer
    Ear, Nose & Throat Journal.2024;[Epub]     CrossRef
  • The Usefulness of Ultrasound-Guided Core Needle Biopsy Compared to Fine Needle Aspiration in Pre-Operative Diagnosis of Cystic-Predominant Parotid Tumors
    Youn Jin Cho, Young Rok Jo, Hyun Jun Hong, Hye Ran Lee
    Korean Journal of Otorhinolaryngology-Head and Neck Surgery.2023; 66(8): 532.     CrossRef
  • The Value of Ultrasound-guided Core Needle Biopsy in Differentiating Benign from Malignant Salivary Gland Lesions
    Mohammad Ali Kazemi, Farzaneh Amini, Bita Kargar, Maryam Lotfi, Keyvan Aghazadeh, Hashem Sharifian, Behnaz Moradi, Javid Azadbakht
    Indian Journal of Otolaryngology and Head & Neck Surgery.2023; 75(2): 266.     CrossRef
  • Schnellschnittdiagnostik bei Tumoren des Trigonum submandibulare
    S. Riemann, A. Knopf
    HNO.2023; 71(3): 164.     CrossRef
  • Myoepithelial Carcinoma Ex Pleomorphic Adenoma of the Submandibular Gland: A Case Report
    Georgia Syrnioti, Antonia Syrnioti, Alharith Abdullah, Xuehui Lui, Ernesto Mendoza
    Cureus.2023;[Epub]     CrossRef
  • Intraductal Carcinoma: The Carcinoma In Situ of the Salivary Gland
    Rhema Thomas, Tijjani Umar, Farzad Borumandi
    Journal of Craniofacial Surgery.2023; 34(5): e432.     CrossRef
  • Fine-Needle Aspiration Cytology for Parotid Tumors
    Masataka Taniuchi, Tetsuya Terada, Ryo Kawata
    Life.2022; 12(11): 1897.     CrossRef
  • Utility of the Milan System for Reporting Salivary Gland Cytology, with focus on the incidence and histologic correlates of atypia of undetermined significance (AUS) and salivary gland neoplasm of uncertain malignant potential (SUMP): A 3‐year institution
    Christopher M. Cormier, Shweta Agarwal
    Cancer Cytopathology.2022; 130(4): 303.     CrossRef
  • Percutaneous CT-Guided Core Needle Biopsies of Head and Neck Masses: Review of 184 Cases at a Single Academic Institution, Common and Special Techniques, Diagnostic Yield, and Safety
    R.W. Jordan, D.P. Shlapak, J.C. Benson, F.E. Diehn, D.K. Kim, V.T. Lehman, G.B. Liebo, A.A. Madhavan, J.M. Morris, P.P. Morris, J.T. Verdoorn, C.M. Carr
    American Journal of Neuroradiology.2022; 43(1): 117.     CrossRef
  • Nodular fasciitis of the submandibular gland
    Ting Suen Wong, Richard Wei Chern Gan, Laszlo Karsai, Bun Yin Winson Wong
    BMJ Case Reports.2022; 15(4): e245584.     CrossRef
  • Validation of the Milan system for reporting salivary gland cytopathology: a single institution’s 10-year experience
    Christopher Felicelli, Joseph Reznicek, Yevgen Chornenkyy, Lucy Jager, Daniel Johnson
    Journal of the American Society of Cytopathology.2022; 11(5): 264.     CrossRef
  • Application of the Milan system for reporting salivary gland cytopathology using cell blocks
    Grégoire B. Morand, Raihanah Alsayegh, Alex M. Mlynarek, Marianne Plourde, Tiffany Mach, Marco A. Mascarella, Michael P. Hier, Livia Florianova, Marc P. Pusztaszeri
    Virchows Archiv.2022; 481(4): 575.     CrossRef
  • Comparisons among the Ultrasonography Prediction Model, Real-Time and Shear Wave Elastography in the Evaluation of Major Salivary Gland Tumors
    Ping-Chia Cheng, Wu-Chia Lo, Chih-Ming Chang, Ming-Hsun Wen, Po-Wen Cheng, Li-Jen Liao
    Diagnostics.2022; 12(10): 2488.     CrossRef
  • A Novel Sonographic Scoring Model in the Prediction of Major Salivary Gland Tumors
    Wu‐Chia Lo, Chih‐Ming Chang, Chi‐Te Wang, Po‐Wen Cheng, Li‐Jen Liao
    The Laryngoscope.2021;[Epub]     CrossRef
  • Assessing the diagnostic accuracy for pleomorphic adenoma and Warthin tumor by employing the Milan System for Reporting Salivary Gland Cytopathology: An international, multi‐institutional study
    Derek B. Allison, Alexander P. Smith, Daniel An, James Adam Miller, Khurram Shafique, Sharon Song, Kartik Viswanathan, Elizabeth Eykman, Rema A. Rao, Austin Wiles, Güliz A. Barkan, Ritu Nayar, Guido Fadda, Celeste N. Powers, Esther Diana Rossi, Momin T. S
    Cancer Cytopathology.2021; 129(1): 43.     CrossRef
  • Magnetic resonance imaging of salivary gland tumours: Key findings for imaging characterisation
    Davide Maraghelli, Michele Pietragalla, Cesare Cordopatri, Cosimo Nardi, Anna Julie Peired, Giandomenico Maggiore, Stefano Colagrande
    European Journal of Radiology.2021; 139: 109716.     CrossRef
  • The Milan System, from Its Introduction to Its Current Adoption in the Diagnosis of Salivary Gland Cytology
    Esther Diana Rossi
    Journal of Molecular Pathology.2021; 2(2): 114.     CrossRef
  • Utility of the Milan system for reporting salivary gland cytopathology during rapid on‐site evaluation (ROSE) of salivary gland aspirates
    Aanchal Kakkar, Mukin Kumar, Priyadarsani Subramanian, Arshad Zubair, Rajeev Kumar, Alok Thakar, Deepali Jain, Sandeep R. Mathur, Venkateswaran K. Iyer
    Cytopathology.2021; 32(6): 779.     CrossRef
  • Contribution of small tissue biopsy and flow cytometry to preoperative cytological categorization of salivary gland fine needle aspirates according to the Milan System: Single center experience on 287 cases
    Tolga Bağlan, Serpil Dizbay Sak, Cevriye Cansız Ersöz, Koray Ceyhan
    Diagnostic Cytopathology.2021; 49(4): 509.     CrossRef
  • Is Milan for kids?: The Milan System for Reporting Salivary Gland Cytology in pediatric patients at an academic children's hospital with cytologic‐histologic correlation
    Swati P. Satturwar, Maren Y. Fuller, Sara E. Monaco
    Cancer Cytopathology.2021; 129(11): 884.     CrossRef
  • Radiographic Interpretation in Oral Medicine and Hospital Dental Practice
    Katherine France, Anwar A.A.Y. AlMuzaini, Mel Mupparapu
    Dental Clinics of North America.2021; 65(3): 509.     CrossRef
  • Carcinoma ex pleomorphic adenoma of major salivary glands: CT and MR imaging findings
    Can Wang, Qiang Yu, Siyi Li, Jingjing Sun, Ling Zhu, Pingzhong Wang
    Dentomaxillofacial Radiology.2021; 50(7): 20200485.     CrossRef
  • Salivary gland carcinoma in children and adolescents: The EXPeRT/PARTNER diagnosis and treatment recommendations
    Aurore Surun, Dominik T. Schneider, Andrea Ferrari, Teresa Stachowicz‐Stencel, Jelena Rascon, Anna Synakiewicz, Abbas Agaimy, Kata Martinova, Denis Kachanov, Jelena Roganovic, Ewa Bien, Gianni Bisogno, Ines B. Brecht, Frédéric Kolb, Juliette Thariat, Anto
    Pediatric Blood & Cancer.2021;[Epub]     CrossRef
  • A Call for Universal Acceptance of the Milan System for Reporting Salivary Gland Cytopathology
    Eric Barbarite, Sidharth V. Puram, Adeeb Derakhshan, Esther D. Rossi, William C. Faquin, Mark A. Varvares
    The Laryngoscope.2020; 130(1): 80.     CrossRef
  • Preoperative biopsy in parotid malignancies: Variation in use and impact on surgical margins
    Liliya Benchetrit, Sina J. Torabi, Elliot Morse, Saral Mehra, Rahmatullah Rahmati, Heather A. Osborn, Benjamin L. Judson
    The Laryngoscope.2020; 130(6): 1450.     CrossRef
  • α‐Synuclein Real‐Time Quaking‐Induced Conversion in the Submandibular Glands of Parkinson's Disease Patients
    Sireesha Manne, Naveen Kondru, Huajun Jin, Vellareddy Anantharam, Xuemei Huang, Arthi Kanthasamy, Anumantha G. Kanthasamy
    Movement Disorders.2020; 35(2): 268.     CrossRef
  • The Accessory Parotid Gland and its Clinical Significance
    Mateusz A. Rosa, Dominik P. Łazarz, Jakub R. Pękala, Bendik Skinningsrud, Sigurd S. Lauritzen, Bernard Solewski, Przemysław A. Pękala, Jerzy A. Walocha, Krzysztof A. Tomaszewski
    Journal of Craniofacial Surgery.2020; 31(3): 856.     CrossRef
  • Comparison of core needle biopsy and fine‐needle aspiration in diagnosis of ma lignant salivary gland neoplasm: Systematic review and meta‐analysis
    Jungheum Cho, Junghoon Kim, Ji Sung Lee, Choong Guen Chee, Youngjune Kim, Sang Il Choi
    Head & Neck.2020; 42(10): 3041.     CrossRef
  • The Milan system for reporting salivary gland cytopathology: The clinical impact so far. Considerations from theory to practice
    Esther Diana Rossi, William C. Faquin
    Cytopathology.2020; 31(3): 181.     CrossRef
  • The role of core needle biopsy in parotid glands lesions with inconclusive fine needle aspiration
    Farrokh Heidari, Firouzeh Heidari, Benyamin Rahmaty, Neda Jafari, Kayvan Aghazadeh, Saeed Sohrabpour, Ebrahim Karimi
    American Journal of Otolaryngology.2020; 41(6): 102718.     CrossRef
  • Role of Fine Needle Aspiration Cytology in the Diagnosis of Parotid Gland Tumors: Analysis of 193 Cases
    Rahim Dhanani, Haissan Iftikhar, Muhammad Sohail Awan, Nida Zahid, Sehrish Nizar Ali Momin
    International Archives of Otorhinolaryngology.2020; 24(04): e508.     CrossRef
  • Cytohistological correlation of salivary gland tumours with emphasis on Milan system for reporting: A novel step towards internal quality assurance
    Anandraj Vaithy.K, ATM Venkat Raghava, E S Keerthika Sri, K R Umadevi
    IP Archives of Cytology and Histopathology Research.2020; 5(4): 283.     CrossRef
  • Diagnosing Recently Defined and Uncommon Salivary Gland Lesions in Limited Cellularity Specimens: Cytomorphology and Ancillary Studies
    Esther Diana Rossi, Zubair Baloch, William Faquin, Liron Pantanowitz
    AJSP: Reviews and Reports.2020; 25(5): 210.     CrossRef
  • Peripheral T Cell Lymphoma of Parotid Gland: A Diagnostic Challenge
    J. G. Aishwarya, Satish Nair, C. N. Patil, Swarna Shivakumar, N. Shrivalli, Ashish Shah
    Indian Journal of Otolaryngology and Head & Neck Surgery.2019; 71(S1): 533.     CrossRef
  • Potential utility of core needle biopsy in the diagnosis of IgG4-related dacryoadenitis and sialadenitis
    Kenichi Takano, Tsuyoshi Okuni, Keisuke Yamamoto, Ryuta Kamekura, Ryoto Yajima, Motohisa Yamamoto, Hiroki Takahashi, Tetsuo Himi
    Modern Rheumatology.2019; 29(2): 393.     CrossRef
  • Retrospective assessment of the effectiveness of the Milan system for reporting salivary gland cytology: A systematic review and meta‐analysis of published literature
    Sahar J Farahani, Zubair Baloch
    Diagnostic Cytopathology.2019; 47(2): 67.     CrossRef
  • Values of fine‐needle aspiration cytology of parotid gland tumors: A review of 996 cases at a single institution
    Manabu Suzuki, Ryo Kawata, Masaaki Higashino, Shuji Nishikawa, Tetsuya Terada, Shin‐Ichi Haginomori, Yoshitaka Kurisu, Yoshinobu Hirose
    Head & Neck.2019; 41(2): 358.     CrossRef
  • Positive Surgical Margins in Submandibular Malignancies: Facility and Practice Variation
    Liliya Benchetrit, Elliot Morse, Benjamin L. Judson, Saral Mehra
    Otolaryngology–Head and Neck Surgery.2019; 161(4): 620.     CrossRef
  • The growth rate and the positive prediction of needle biopsy of clinically diagnosed Warthin’s tumor
    Jungirl Seok, Woo-Jin Jeong, Soon-Hyun Ahn, Young Ho Jung
    European Archives of Oto-Rhino-Laryngology.2019; 276(7): 2091.     CrossRef
  • The Difference in the Clinical Features Between Carcinoma ex Pleomorphic Adenoma and Pleomorphic Adenoma
    Jungirl Seok, Se Jin Hyun, Woo-Jin Jeong, Soon-Hyun Ahn, Hyojin Kim, Young Ho Jung
    Ear, Nose & Throat Journal.2019; 98(8): 504.     CrossRef
  • Fine‐needle aspiration cytology and radiological imaging in parotid gland tumours: Our experience in 103 patients
    Clare Perkins, Edward Toll, Philip Reece
    Clinical Otolaryngology.2019; 44(6): 1124.     CrossRef
  • Ultrasound‐guided core needle biopsy in salivary glands: A meta‐analysis
    Hee Joon Kim, Jong Seung Kim
    The Laryngoscope.2018; 128(1): 118.     CrossRef
  • Accuracy and effectiveness of ultrasound-guided core-needle biopsy in the diagnosis of focal lesions in the salivary glands
    Jose Luis del Cura, Gloria Coronado, Rosa Zabala, Igone Korta, Ignacio López
    European Radiology.2018; 28(7): 2934.     CrossRef
  • The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC): an ASC-IAC–sponsored system for reporting salivary gland fine-needle aspiration
    Esther Diana Rossi, Zubair Baloch, Marc Pusztaszeri, William C. Faquin
    Journal of the American Society of Cytopathology.2018; 7(3): 111.     CrossRef
  • Routine and Advanced Ultrasound of Major Salivary Glands
    Kunwar Suryaveer Singh Bhatia, Yuk-Ling Dai
    Neuroimaging Clinics of North America.2018; 28(2): 273.     CrossRef
  • The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC): An ASC-IAC-Sponsored System for Reporting Salivary Gland Fine-Needle Aspiration
    Esther Diana Rossi, Zubair W. Baloch, Marc Pusztaszeri, William C. Faquin
    Acta Cytologica.2018; 62(3): 157.     CrossRef
  • Evaluation and diagnosis of salivary gland neoplasms
    Erica Jackson Mayland, Anna M. Pou
    Operative Techniques in Otolaryngology-Head and Neck Surgery.2018; 29(3): 129.     CrossRef
  • Feasibility and Safety of Multicenter Tissue and Biofluid Sampling for α-Synuclein in Parkinson’s Disease: The Systemic Synuclein Sampling Study (S4)
    Lana M. Chahine, Thomas G. Beach, Nicholas Seedorff, Chelsea Caspell-Garcia, Christopher S. Coffey, Michael Brumm, Charles H. Adler, Geidy E. Serrano, Carly Linder, Sherri Mosovsky, Tatiana Foroud, Holly Riss, Dixie Ecklund, John Seibyl, Danna Jennings, V
    Journal of Parkinson's Disease.2018; 8(4): 517.     CrossRef
  • Preoperative diagnostic of parotid gland neoplasms: fine-needle aspiration cytology or core needle biopsy?
    Peter Zbären, Asterios Triantafyllou, Kenneth O. Devaney, Vincent Vander Poorten, Henrik Hellquist, Alessandra Rinaldo, Alfio Ferlito
    European Archives of Oto-Rhino-Laryngology.2018; 275(11): 2609.     CrossRef
  • A comparison study of the reporting systems for salivary gland fine needle aspirations: Are they really different?
    Diana Montezuma, Sule Canberk, Ozlem Aydın, Mehmet Polat Dermirhas, André F. Vieira, Süha Goksel, Ümit İnce, Fernando Schmitt
    Diagnostic Cytopathology.2018; 46(10): 859.     CrossRef
  • Pediatric salivary gland carcinomas: Diagnostic and therapeutic management
    Céleste Rebours, Vincent Couloigner, Louise Galmiche, Odile Casiraghi, Cécile Badoual, Sabah Boudjemaa, Anthony Chauvin, Monique Elmaleh, Brice Fresneau, Sylvie Fasola, Erea‐Noël Garabédian, Thierry Van Den Abeele, Daniel Orbach
    The Laryngoscope.2017; 127(1): 140.     CrossRef
  • Agreement between rapid on‐site evaluation and the final cytological diagnosis of salivary gland specimens
    S. Wangsiricharoen, S. Lekawanvijit, S. Rangdaeng
    Cytopathology.2017; 28(4): 321.     CrossRef
  • Mesenchymal neoplasms of the head and neck: a cytopathologic analysis on fine needle aspiration
    James Lee, Samia Kazmi, Christopher J. VandenBussche, Syed Z. Ali
    Journal of the American Society of Cytopathology.2017; 6(3): 105.     CrossRef
  • Clinical Results of Surgical Treatment in Parotid Tumors
    Ahmet Kara
    Journal of Otolaryngology-ENT Research.2017;[Epub]     CrossRef
  • Parotid gland metastases of distant primary tumours: A diagnostic challenge
    Achim M. Franzen, Thomas Günzel, Anja Lieder
    Auris Nasus Larynx.2016; 43(2): 187.     CrossRef
  • Modern Radiology in the Management of Head and Neck Cancer
    G.J.C. Burkill, R.M. Evans, V.V. Raman, S.E.J. Connor
    Clinical Oncology.2016; 28(7): 440.     CrossRef
  • Fine‐needle aspiration and core needle biopsy: An update on 2 common minimally invasive tissue sampling modalities
    Paul A. VanderLaan
    Cancer Cytopathology.2016; 124(12): 862.     CrossRef
  • Staging and follow-up of high-grade malignant salivary gland tumours: The role of traditional versus functional imaging approaches – A review
    Nicole Freling, Flavio Crippa, Roberto Maroldi
    Oral Oncology.2016; 60: 157.     CrossRef
  • Biopsy of parotid masses: Review of current techniques
    Sananda Haldar, Joseph D Sinnott, Kemal M Tekeli, Samuel S Turner, David C Howlett
    World Journal of Radiology.2016; 8(5): 501.     CrossRef
  • Review on the applications of ultrasonography in dentomaxillofacial region
    Şehrazat Evirgen
    World Journal of Radiology.2016; 8(1): 50.     CrossRef
  • Comprehensive Cytomorphologic Analysis of Pulmonary Adenoid Cystic Carcinoma: Comparison to Small Cell Carcinoma and Non-pulmonary Adenoid Cystic Carcinoma
    Seokhwi Kim, Jinah Chu, Hojoong Kim, Joungho Han
    Journal of Pathology and Translational Medicine.2015; 49(6): 511.     CrossRef
Mdm2 and p53 Expression in Radiation-Induced Sarcomas of the Head and Neck: Comparison with De Novo Sarcomas
Min Jeong Song, Joon Seon Song, Jong-Lyel Roh, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Sung Bae Kim, Sang-wook Lee, Kyung-Ja Cho
Korean J Pathol. 2014;48(5):346-350.   Published online October 27, 2014
DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.5.346
  • 6,820 View
  • 41 Download
  • 3 Crossref
AbstractAbstract PDF
Background: The pathogenesis of radiation-induced sarcomas (RISs) is not well known. In RIS, TP53 mutations are frequent, but little is known about Mdm2-p53 interaction, which is a recent therapeutic target of sarcomas. Methods: We studied the immunohistochemical expression of Mdm2 and p53 of 8 RISs. The intervals between radiation therapy and diagnosis of secondary sarcomas ranged from 3 to 17 years. Results: Mdm2 expression was more common in de novo sarcomas than RISs (75% vs 37.5%), and p53 expression was more common in RISs than in de novo cases (75% vs 37.5%). While half of the RISs were Mdm2(–)/p53(+), none of de novo cases showed such combination; while half of de novo sarcomas were Mdm2(+)/p53(–), which are a candidate group of Mdm2 inhibitors, only 1 RIS showed such a combination. Variable immunoprofiles observed in both groups did not correlate with tumor types, except that all of 2 myxofibrosarcomas were Mdm2(+)/p53(+). Conclusions: In conclusion, we speculated that both radiation- induced and de novo sarcomagenesis are not due to a unique genetic mechanism. Mdm2- expression without p53 overexpression in 1 case of RIS decreases the future possibility of applying Mdm2 inhibitors on a subset of these difficult tumors.

Citations

Citations to this article as recorded by  
  • Radiation-Induced Sarcomas of the Head and Neck: A Systematic Review
    Andrés Coca-Pelaz, Antti A. Mäkitie, Primož Strojan, June Corry, Avraham Eisbruch, Jonathan J. Beitler, Sandra Nuyts, Robert Smee, Johannes A. Langendijk, William M. Mendenhall, Cesare Piazza, Alessandra Rinaldo, Alfio Ferlito
    Advances in Therapy.2021; 38(1): 90.     CrossRef
  • Genomic Characterization of Radiation-Induced Intracranial Undifferentiated Pleomorphic Sarcoma
    Christopher S. Hong, Edwin Partovi, James Clune, Anita Huttner, Henry S. Park, Sacit Bulent Omay, Balraj Mittal
    Case Reports in Genetics.2021; 2021: 1.     CrossRef
  • Radiation-Induced Sarcoma of the Head and Neck: A Review of the Literature
    Lorenzo Giannini, Fabiola Incandela, Marco Fiore, Alessandro Gronchi, Silvia Stacchiotti, Claudia Sangalli, Cesare Piazza
    Frontiers in Oncology.2018;[Epub]     CrossRef
Human Papillomavirus Prevalence and Cell Cycle Related Protein Expression in Tonsillar Squamous Cell Carcinomas of Korean Patients with Clinicopathologic Analysis
Miji Lee, Sung Bae Kim, Sang-wook Lee, Jong-Lyel Roh, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Kyung-Ja Cho
Korean J Pathol. 2013;47(2):148-157.   Published online April 24, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.2.148
  • 6,877 View
  • 48 Download
  • 5 Crossref
AbstractAbstract PDF
Background

Human papillomavirus (HPV)-related tonsillar squamous cell carcinoma (TSCC) has recently been characterized as a distinct subset with a favorable prognosis. The prevalence and clinicopathologic significance of HPV-related TSCC in Koreans are not well known.

Methods

HPV in situ hybridization (ISH) accompanied by p53, p16, pRb, and cyclin D1 immunohistochemical staining were performed on 89 resection cases of TSCC from 2000 through 2010.

Results

HPV was detected by ISH in 59 of 89 cases (66.3%). HPV-positive TSCCs were more common in younger ages (p=0.005), and tumor sizes were smaller in the HPV-positive compared to the HPV-negative group (p=0.040). Positive HPV staining was significantly correlated with p16 expression (p<0.001), pRb inactivation (p=0.003), and cyclin D1 down-regulation (p<0.001) but not with p53 expression (p=0.334). Seventeen cases that showed p16-immunopositivity with HPV-negativity by ISH were retested by HPV typing; HPV DNA was not detected in all cases. There was no significant difference between HPV-positive and HPV-negative patients either in the disease-specific survival (DSS, p=0.857) or overall survival (p=0.910). Furthermore, pRb-inactivated cases showed better DSS (p=0.023), and p53-positive cases showed worse DSS (p=0.001).

Conclusions

Although high HPV prevalence was noted, it was not correlated with histopathologic findings or survival benefit. In addition to p53 expression, pRb inactivation along with p16 overexpression and down-regulation of cyclin D1 are thought to be important pathogenetic steps for developing TSCCs.

Citations

Citations to this article as recorded by  
  • Assessment of the Mutation Profile of Tonsillar Squamous Cell Carcinomas Using Targeted Next-Generation Sequencing
    Ha Young Park, Joong Seob Lee, Jee Hye Wee, Jeong Wook Kang, Eun Soo Kim, Taeryool Koo, Hee Sung Hwang, Hyo Jung Kim, Ho Suk Kang, Hyun Lim, Nan Young Kim, Eun Sook Nam, Seong Jin Cho, Mi Jung Kwon
    Biomedicines.2023; 11(3): 851.     CrossRef
  • Clinicopathologic characterization of cervical metastasis from an unknown primary tumor: a multicenter study in Korea
    Miseon Lee, Uiree Jo, Joon Seon Song, Youn Soo Lee, Chang Gok Woo, Dong-Hoon Kim, Jung Yeon Kim, Sun Och Yoon, Kyung-Ja Cho
    Journal of Pathology and Translational Medicine.2023; 57(3): 166.     CrossRef
  • Negative Prognostic Implication of TERT Promoter Mutations in Human Papillomavirus–Negative Tonsillar Squamous Cell Carcinoma Under the New 8th AJCC Staging System
    Hyunchul Kim, Mi Jung Kwon, Bumjung Park, Hyo Geun Choi, Eun Sook Nam, Seong Jin Cho, Kyueng-Whan Min, Eun Soo Kim, Hee Sung Hwang, Mineui Hong, Taeryool Koo, Hyo Jung Kim
    Indian Journal of Surgical Oncology.2021; 12(S1): 134.     CrossRef
  • Prevalence of high-risk human papillomavirus and its genotype distribution in head and neck squamous cell carcinomas
    Yuil Kim, Young-Hoon Joo, Min-Sik Kim, Youn Soo Lee
    Journal of Pathology and Translational Medicine.2020; 54(5): 411.     CrossRef
  • Frequent hepatocyte growth factor overexpression and low frequency of c-Met gene amplification in human papillomavirus–negative tonsillar squamous cell carcinoma and their prognostic significances
    Mi Jung Kwon, Dong Hoon Kim, Hye-Rim Park, Hyung Sik Shin, Ji Hyun Kwon, Dong Jin Lee, Jin Hwan Kim, Seong Jin Cho, Eun Sook Nam
    Human Pathology.2014; 45(7): 1327.     CrossRef
Finding and Characterizing Mammary Analogue Secretory Carcinoma of the Salivary Gland
Min Jung Jung, Joon Seon Song, Sang Yoon Kim, Soon Yuhl Nam, Jong-Lyel Roh, Seung-Ho Choi, Sung-Bae Kim, Kyung-Ja Cho
Korean J Pathol. 2013;47(1):36-43.   Published online February 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.1.36
  • 12,020 View
  • 93 Download
  • 71 Crossref
AbstractAbstract PDF
Background

A new tumor entity of the salivary glands, mammary analogue secretory carcinoma (MASC) with ETV6-NTRK3 translocation, has recently been proposed. MASC was originally diagnosed as adenocarcinoma, not otherwise specified (ANOS), or acinic cell carcinoma (AciCC) by the current World Health Organization classification. We aimed to identify MASC cases by molecular tests, and to characterize their clinical, histological, and immunohistochemical features.

Methods

Thirty cases of MASC candidates were selected after review of 196 salivary gland tumors, and subjected to break-apart ETV6 fluorescence in situ hybridization (FISH), and immunohistochemical study for S100 protein, gross cystic disease fluid protein 15, DOG1, estrogen receptor, and progesterone receptor.

Results

Valid FISH results were obtained in 23 cases, and 13 positive cases were retrieved. MASCs were histologically varied, and the most frequent features observed in 10 cases were low-grade papillary/cystic/glandular patterns, intraluminal secretory materials, ovoid/wrinkled nuclei, and relatively abundant granular eosinophilic cytoplasms, corresponding to papillary-cystic or follicular types of AciCC. All cases showed diffuse immunopositivity for S100 protein. Three cases developed recurrences, but all patients remained alive.

Conclusions

MASC could be a molecularly well-defined salivary gland neoplasm, encompassing some portions of AciCC and ANOS, but its histological spectrum and clinical implication require further investigation.

Citations

Citations to this article as recorded by  
  • Salivary Gland Secretory Carcinoma; Review of 13 Years World‐Wide Experience and Meta‐Analysis
    Eyal Yosefof, Tomer Boldes, Daniel Dan, Eyal Robenshtok, Yulia Strenov, Gideon Bachar, Thomas Shpitzer, Aviram Mizrachi
    The Laryngoscope.2024; 134(4): 1716.     CrossRef
  • Salivary gland secretory carcinoma presenting as a cervical soft tissue mass: a case report
    Parisa Mokhles, Alireza Sadeghipour, Pegah Babaheidarian, Saleh Mohebbi, Zahra Keshtpour Amlashi, Mohammad Hadi Gharib, Mohammad Saeid Ahmadi, Zeinab Khastkhodaei
    Journal of Medical Case Reports.2024;[Epub]     CrossRef
  • Mammary analogue secretory carcinoma of the head and neck — Clinicopathological, imaging features and prognosis analysis
    Runjia Liu, Chuanzheng Sun, Likang Zhao, Shiyu Zhou, Tao Xie, Ji Zhang, Dengpeng Tang, Lei Li, Yan Xi
    Journal of Radiation Research and Applied Sciences.2024; : 100914.     CrossRef
  • Metastatic salivary gland mammary analogue secretory carcinoma (MASC) of parotid gland – A rare case report in the literature review
    Aynur Aliyeva, Ziya Karimov, Togay Muderris
    Acta Oto-Laryngologica Case Reports.2023; 8(1): 38.     CrossRef
  • Secretory carcinoma of minor salivary glands of buccal mucosa: A case report and review of the literature
    Noshad Ali Langah, Abdul Ahad, Shayan Khalid Ghaloo, Muhammad Faisal, Raza Tasawar Hussain, Fareed Akbar Shah
    International Journal of Surgery Case Reports.2023; 107: 108357.     CrossRef
  • An Underappreciated Cytomorphological Feature of Secretory Carcinoma of Salivary Gland on Fine Needle Aspiration Biopsy: Case Report with Literature Review
    Yinan Hua, Bing Leng, Kenneth E. Youens, Lina Liu
    Head and Neck Pathology.2022; 16(2): 567.     CrossRef
  • Clinicopathological investigation of secretory carcinoma cases including a successful treatment outcome using entrectinib for high-grade transformation: a case report
    Kensuke Suzuki, Hiroshi Harada, Masayuki Takeda, Chisato Ohe, Yoshiko Uemura, Akihiko Kawahara, Shunsuke Sawada, Akira Kanda, Bhaswati Sengupta, Hiroshi Iwai
    BMC Medical Genomics.2022;[Epub]     CrossRef
  • DOG1 as an Immunohistochemical Marker of Acinic Cell Carcinoma: A Systematic Review and Meta-Analysis
    Vincenzo Fiorentino, Patrizia Straccia, Pietro Tralongo, Teresa Musarra, Francesco Pierconti, Maurizio Martini, Guido Fadda, Esther Diana Rossi, Luigi Maria Larocca
    International Journal of Molecular Sciences.2022; 23(17): 9711.     CrossRef
  • Secretory carcinoma of the sinonasal cavity and pharynx: A retrospective analysis of four cases and literature review
    Changli Yue, Xiaoli Zhao, Donglin Ma, Yingshi Piao
    Annals of Diagnostic Pathology.2022; 61: 152052.     CrossRef
  • Secretory carcinoma of the salivary gland: a multi‐institutional clinicopathologic study of 90 cases with emphasis on grading and prognostic factors
    Bin Xu, Kartik Viswanathan, Kavita Umrau, Thair A. D. Al‐Ameri, Snjezana Dogan, Kelly Magliocca, Ronald A. Ghossein, Nicole A. Cipriani, Nora Katabi
    Histopathology.2022; 81(5): 670.     CrossRef
  • A systematic review of secretory carcinoma of the salivary gland: where are we?
    Lísia Daltro Borges Alves, Andreia Cristina de Melo, Thayana Alves Farinha, Luiz Henrique de Lima Araujo, Leandro de Souza Thiago, Fernando Luiz Dias, Héliton Spíndola Antunes, Ana Lucia Amaral Eisenberg, Luiz Claudio Santos Thuler, Daniel Cohen Goldember
    Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology.2021; 132(4): e143.     CrossRef
  • A case report of surgical resection of secretory carcinoma in the maxillary and ethmoid sinus
    Kurt Willis, Martin Bullock, Matthew H. Rigby
    International Journal of Surgery Case Reports.2021; 81: 105750.     CrossRef
  • High‐grade salivary gland carcinoma with the ETV6‐NTRK3 gene fusion: A case report and literature review of secretory carcinoma with high‐grade transformation
    Satsuki Asai, Shinji Sumiyoshi, Yosuke Yamada, Ichiro Tateya, Toshitaka Nagao, Sachiko Minamiguchi, Hironori Haga
    Pathology International.2021; 71(6): 427.     CrossRef
  • High-grade Transformation/Dedifferentiation in Salivary Gland Carcinomas: Occurrence Across Subtypes and Clinical Significance
    Alena Skalova, Ilmo Leivo, Henrik Hellquist, Abbas Agaimy, Roderick H.W. Simpson, Göran Stenman, Vincent Vander Poorten, Justin A. Bishop, Alessandro Franchi, Juan C. Hernandez-Prera, David Slouka, Stefan M. Willems, Kerry D. Olsen, Alfio Ferlito
    Advances in Anatomic Pathology.2021; 28(3): 107.     CrossRef
  • Radiological features of head and neck mammary analogue secretory carcinoma: 11 new cases with a systematic review of 29 cases reported in 28 publications
    Ryo Kurokawa, Mariko Kurokawa, Akira Baba, Yoshiaki Ota, Toshio Moritani, Ashok Srinivasan
    Neuroradiology.2021; 63(11): 1901.     CrossRef
  • A case of secretory carcinoma of the salivary glands in the lower lip
    Reiko OHARA, Haruki SATO, Kensuke NAGANAWA, Taihei HAYAKAWA, Tatsuya KATAOKA, Ichiro OH-IWA
    Japanese Journal of Oral and Maxillofacial Surgery.2021; 67(2): 83.     CrossRef
  • Undifferentiated and dedifferentiated head and neck carcinomas
    Alessandro Franchi, Alena Skalova
    Seminars in Diagnostic Pathology.2021; 38(6): 127.     CrossRef
  • Cytopathological Findings of Secretory Carcinoma of the Salivary Gland and the Diagnostic Utility of Giemsa Staining
    Yuria Egusa, Midori Filiz Nishimura, Satoko Baba, Kengo Takeuchi, Takuma Makino, Tomoyasu Tachibana, Asami Nishikori, Azusa Fujita, Hiroyuki Yanai, Yasuharu Sato
    Diagnostics.2021; 11(12): 2284.     CrossRef
  • Diagnosis and treatment of secretory carcinoma arising from the oral minor salivary gland
    Masaru Ogawa, Satoshi Yokoo, Takahiro Yamaguchi, Keisuke Suzuki, Mai Seki-Soda, Takahiro Shimizu, Jun Kurihara, Takaya Makiguchi
    Medicine.2021; 100(51): e28390.     CrossRef
  • A biphasic sessile mass of the buccal mucosa
    Tiffany M. Peters, James A. Phero, Brent A. Golden, Alice E. Curran
    Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology.2020; 130(6): 612.     CrossRef
  • Don't stop the champions of research now: a brief history of head and neck pathology developments
    Lester D.R. Thompson, James S. Lewis, Alena Skálová, Justin A. Bishop
    Human Pathology.2020; 95: 1.     CrossRef
  • High Grade Transformation in Mucoepidermoid Carcinoma of the Minor Salivary Gland with Polyploidy of the Rearranged MAML2 Gene
    Hyun Lee, Jong-Lyel Roh, Young-Jun Choi, Jene Choi, Kyung-Ja Cho
    Head and Neck Pathology.2020; 14(3): 822.     CrossRef
  • Pan‐Trk immunohistochemistry is a sensitive and specific ancillary tool for diagnosing secretory carcinoma of the salivary gland and detecting ETV6–NTRK3 fusion
    Bin Xu, Mohamed R Haroon Al Rasheed, Cristina R Antonescu, Deepu Alex, Denise Frosina, Ronald Ghossein, Achim A Jungbluth, Nora Katabi
    Histopathology.2020; 76(3): 375.     CrossRef
  • Characterization of novel genetic alterations in salivary gland secretory carcinoma
    Kiyong Na, Juan C. Hernandez-Prera, Jae-Yol Lim, Ha Young Woo, Sun Och Yoon
    Modern Pathology.2020; 33(4): 541.     CrossRef
  • Mammary analogue secretory carcinoma: An Indian experience of a novel entity
    Zeba Nisar, JaydeepN Pol, RakhiV Jagdale, MadhuraD Phadke, GirishA Kadkol
    Indian Journal of Pathology and Microbiology.2020; 63(5): 134.     CrossRef
  • Secretory Carcinoma of Salivary Gland with High-Grade Histology Arising in Hard Palate: A Case Report
    Kiyofumi Takabatake, Keisuke Nakano, Hotaka Kawai, Saori Yoshida, Haruka Omori, May Wathone Oo, Shan Qiusheng, Kenichiro Uchida, Katsuaki Mishima, Hitoshi Nagatsuka
    Reports — Medical Cases, Images, and Videos.2020; 3(2): 6.     CrossRef
  • Secretory carcinoma of the salivary gland (mammary analogue secretory carcinoma) in children
    I. V. Sidorov, I. S. Kletskaya, D. M. Konovalov
    Arkhiv patologii.2020; 82(2): 43.     CrossRef
  • Secretory carcinoma of the major salivary gland: Provincial population‐based analysis of clinical behavior and outcomes
    Gareth Ayre, Martin Hyrcza, Jonn Wu, Eric Berthelet, Alena Skálová, Tom Thomson
    Head & Neck.2019; 41(5): 1227.     CrossRef
  • Higher Ki67 Index, Nodal Involvement, and Invasive Growth Were High Risk Factors for Worse Prognosis in Conventional Mammary Analogue Secretory Carcinoma
    Jingjing Sun, Lizhen Wang, Zhen Tian, Yuhua Hu, Ronghui Xia, Jiang Li
    Journal of Oral and Maxillofacial Surgery.2019; 77(6): 1187.     CrossRef
  • Mammary analogue secretory carcinoma of salivary gland diagnosed on submandibular gland cytology: A case report and review of the literature
    Ethar Al‐Husseinawi, Soheila Hamidpour, Evanthia Omoscharka
    Cytopathology.2019; 30(3): 318.     CrossRef
  • Secretory Carcinoma of Minor Salivary Gland in Buccal Mucosa: A Case Report and Review of the Literature
    Durga Paudel, Michiko Nishimura, Bhoj Raj Adhikari, Daichi Hiraki, Aya Onishi, Tetsuro Morikawa, Puja Neopane, Sarita Giri, Koki Yoshida, Jun Sato, Masayuki Ono, Yoshitaka Kamino, Hiroki Nagayasu, Yoshihiro Abiko
    Case Reports in Pathology.2019; 2019: 1.     CrossRef
  • Estrogen Receptor, Progesterone Receptor, and HER-2 Expression in Recurrent Pleomorphic Adenoma
    Ana Amélia de Souza, Albina Altemani, Ney Soares de Araujo, Lucas Novaes Texeira, Vera Cavalcanti de Araújo, Andresa Borges Soares
    Clinical Pathology.2019; 12: 2632010X1987338.     CrossRef
  • Sinonasal Secretory Carcinoma of Salivary Gland with High Grade Transformation: A Case Report of this Under-Recognized Diagnostic Entity with Prognostic and Therapeutic Implications
    Bin Xu, Ruth Aryeequaye, Lu Wang, Nora Katabi
    Head and Neck Pathology.2018; 12(2): 274.     CrossRef
  • Primary mammary analogue secretory carcinoma of the lung: a case report
    Tao Huang, Jonathan B. McHugh, Gerald J. Berry, Jeffrey L. Myers
    Human Pathology.2018; 74: 109.     CrossRef
  • Salivary Secretory Carcinoma With a Novel ETV6-MET Fusion
    Lisa M. Rooper, Theodoros Karantanos, Yi Ning, Justin A. Bishop, Sarah W. Gordon, Hyunseok Kang
    American Journal of Surgical Pathology.2018; 42(8): 1121.     CrossRef
  • Secretory carcinoma: The eastern Canadian experience and literature review
    David Forner, Martin Bullock, Daniel Manders, Timothy Wallace, Christopher J. Chin, Liane B. Johnson, Matthew H. Rigby, Jonathan R. Trites, Mark S. Taylor, Robert D. Hart
    Journal of Otolaryngology - Head & Neck Surgery.2018;[Epub]     CrossRef
  • Newly described salivary gland tumors
    Alena Skalova, Michal Michal, Roderick HW Simpson
    Modern Pathology.2017; 30: S27.     CrossRef
  • Diagnóstico, tratamiento y seguimiento de un tumor de reciente descripción: el carcinoma análogo secretor de mama (MASC) de glándula salival. A propósito de 2 nuevos casos
    Marina Alexandra Gavín-Clavero, M. Victoria Simón-Sanz, Ana M. López-López, Alberto Valero-Torres, Esther Saura-Fillat
    Revista Española de Cirugía Oral y Maxilofacial.2017; 39(4): 221.     CrossRef
  • Systematic review of mammary analog secretory carcinoma of salivary glands at 7 years after description
    Bacem A. Khalele
    Head & Neck.2017; 39(6): 1243.     CrossRef
  • Salivary Gland Secretory Carcinoma With High-Grade Transformation, CDKN2A/B Loss, Distant Metastasis, and Lack of Sustained Response to Crizotinib
    Nicole A. Cipriani, Elizabeth A. Blair, Joshua Finkle, Jennifer L. Kraninger, Christopher M. Straus, Victoria M. Villaflor, Daniel Thomas Ginat
    International Journal of Surgical Pathology.2017; 25(7): 613.     CrossRef
  • A systematic review including an additional pediatric case report: Pediatric cases of mammary analogue secretory carcinoma
    Amanda L. Ngouajio, Sarah M. Drejet, D. Ryan Phillips, Don-John Summerlin, John P. Dahl
    International Journal of Pediatric Otorhinolaryngology.2017; 100: 187.     CrossRef
  • Newly Described Entities in Salivary Gland Pathology
    Alena Skálová, Douglas R. Gnepp, James S. Lewis, Jennifer L. Hunt, Justin A. Bishop, Henrik Hellquist, Alessandra Rinaldo, Vincent Vander Poorten, Alfio Ferlito
    American Journal of Surgical Pathology.2017; 41(8): e33.     CrossRef
  • Mammary Analogue Secretory Carcinoma of Salivary Glands: Diagnostic Pitfall with Distinct Immunohistochemical Profile and Molecular Features
    Oliver Bissinger, Carolin Götz, Andreas Kolk, Henning A. Bier, Abbas Agaimy, Henning Frenzel, Sven Perner, Julika Ribbat-Idel, Klaus Dietrich Wolff, Wilko Weichert, Caroline Mogler
    Rare Tumors.2017; 9(3): 89.     CrossRef
  • Mammary Analogue Secretory Carcinoma of Salivary Gland. A Case Report Emphasizing its Diagnostic Histological, Immunohistochemistry and Molecular Findings
    Monalisa Hui, Shantveer G Uppin, Vamshi Krishna Thamtam, Abhiram Kalle
    International Journal of Head and Neck Surgery.2017; 8(4): 160.     CrossRef
  • A case of mammary analog secretory carcinoma of the lower lip
    Takako Aizawa, Taro Okui, Ken Kitagawa, Yoshikazu Kobayashi, Koji Satoh, Hideki Mizutani
    Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2016; 28(3): 277.     CrossRef
  • Mammary analogue secretory carcinoma of parotid: Is preoperative cytological diagnosis possible?
    Nikita Oza, Kintan Sanghvi, Tanuja Shet, Asawari Patil, Santosh Menon, Mukta Ramadwar, Shubhada Kane
    Diagnostic Cytopathology.2016; 44(6): 519.     CrossRef
  • Lysozyme Expression Can be Useful to Distinguish Mammary Analog Secretory Carcinoma from Acinic Cell Carcinoma of Salivary Glands
    Fernanda Viviane Mariano, Camila Andrea Concha Gómez, Juliana de Souza do Nascimento, Harim Tavares dos Santos, Erika Said Egal, Victor Angelo Martins Montalli, Pablo Agustin Vargas, Oslei Paes de Almeida, Albina Altemani
    Head and Neck Pathology.2016; 10(4): 429.     CrossRef
  • Cytogenetic and immunohistochemical characterization of mammary analogue secretory carcinoma of salivary glands
    Syed A. Khurram, Jemel Sultan-Khan, Neil Atkey, Paul M. Speight
    Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology.2016; 122(6): 731.     CrossRef
  • The role of DOG1 immunohistochemistry in dermatopathology
    Keisuke Goto
    Journal of Cutaneous Pathology.2016; 43(11): 974.     CrossRef
  • Extended immunologic and genetic lineage of mammary analogue secretory carcinoma of salivary glands
    Hao Ni, Xue-ping Zhang, Xiao-tong Wang, Qiu-yuan Xia, Jing-huan Lv, Xuan Wang, Shan-shan Shi, Rui Li, Xiao-jun Zhou, Qiu Rao
    Human Pathology.2016; 58: 97.     CrossRef
  • A New Hitherto Unreported Histopathologic Manifestation of Mammary Analogue Secretory Carcinoma: “Masked MASC” Associated With Low-grade Mucinous Adenocarcinoma and Low-grade In Situ Carcinoma Components
    Fredrik Petersson, Michael Michal, Dmitry V. Kazakov, Petr Grossmann, Michal Michal
    Applied Immunohistochemistry & Molecular Morphology.2016; 24(9): e80.     CrossRef
  • Papillary-cystic pattern is characteristic in mammary analogue secretory carcinomas but is rarely observed in acinic cell carcinomas of the salivary gland
    Min-Shu Hsieh, Yueh-Hung Chou, Shin-Joe Yeh, Yih-Leong Chang
    Virchows Archiv.2015; 467(2): 145.     CrossRef
  • Mammary analog secretory carcinoma, low-grade salivary duct carcinoma, and mimickers: a comparative study
    Todd M Stevens, Andra O Kovalovsky, Claudia Velosa, Qiuying Shi, Qian Dai, Randall P Owen, Walter C Bell, Shi Wei, Pamela A Althof, Jennifer N Sanmann, Larissa Sweeny, William R Carroll, Gene P Siegal, Martin J Bullock, Margaret Brandwein-Gensler
    Modern Pathology.2015; 28(8): 1084.     CrossRef
  • Aspiration cytology of mammary analogue secretory carcinoma of the salivary gland
    Min Jung Jung, Sang Yoon Kim, Soon Yuhl Nam, Jong‐Lyel Roh, Seung‐Ho Choi, Jeong Hyun Lee, Jung Hwan Baek, Kyung‐Ja Cho
    Diagnostic Cytopathology.2015; 43(4): 287.     CrossRef
  • A Unique Case of a Cutaneous Lesion Resembling Mammary Analog Secretory Carcinoma
    Jennifer Albus, Jacqueline Batanian, Bruce M. Wenig, Claudia I. Vidal
    The American Journal of Dermatopathology.2015; 37(4): e41.     CrossRef
  • Mammary analogue secretory carcinoma of salivary glands: a new entity associated with ETV6 gene rearrangement
    Hanna Majewska, Alena Skálová, Dominik Stodulski, Adéla Klimková, Petr Steiner, Czesław Stankiewicz, Wojciech Biernat
    Virchows Archiv.2015; 466(3): 245.     CrossRef
  • A comparative immunohistochemistry study of diagnostic tools in salivary gland tumors: usefulness of mammaglobin, gross cystic disease fluid protein 15, and p63 cytoplasmic staining for the diagnosis of mammary analog secretory carcinoma?
    Fabrice Projetti, Magali Lacroix‐Triki, Elie Serrano, Sebastien Vergez, Béatrice Herbault Barres, Julie Meilleroux, Marie‐Bernadette Delisle, Emmanuelle Uro‐Coste
    Journal of Oral Pathology & Medicine.2015; 44(4): 244.     CrossRef
  • Mammary Analogue Secretory Carcinoma of Salivary Glands
    Yohei Ito, Kenichiro Ishibashi, Ayako Masaki, Kana Fujii, Yukio Fujiyoshi, Hideo Hattori, Daisuke Kawakita, Manabu Matsumoto, Satoru Miyabe, Kazuo Shimozato, Toshitaka Nagao, Hiroshi Inagaki
    American Journal of Surgical Pathology.2015; 39(5): 602.     CrossRef
  • Cytopathological features of mammary analogue secretory carcinoma—Review of literature
    Maiko Takeda, Takahiko Kasai, Kohei Morita, Mao Takeuchi, Takeshi Nishikawa, Akinori Yamashita, Shinji Mikami, Hiroshi Hosoi, Chiho Ohbayashi
    Diagnostic Cytopathology.2015; 43(2): 131.     CrossRef
  • Mammary Analog Secretory Carcinoma of Salivary Glands
    Justin A. Bishop
    Pathology Case Reviews.2015; 20(1): 7.     CrossRef
  • Diagnostic utility of phosphorylated signal transducer and activator of transcription 5 immunostaining in the diagnosis of mammary analogue secretory carcinoma of the salivary gland: A comparative study of salivary gland cancers
    Akihiko Kawahara, Tomoki Taira, Hideyuki Abe, Yorihiko Takase, Takashi Kurita, Eiji Sadashima, Satoshi Hattori, Ichio Imamura, Shinji Matsumoto, Hitomi Fujisaki, Kazunobu Sueyoshi, Jun Akiba, Masayoshi Kage
    Cancer Cytopathology.2015; 123(10): 603.     CrossRef
  • A Case of Mammary Analogue Secretory Carcinoma Arising from Parotid Gland
    Hee Tae Kim, Cha Hee Lee, Han Su Kim, Hae Sang Park
    Korean Journal of Otorhinolaryngology-Head and Neck Surgery.2015; 58(8): 563.     CrossRef
  • WITHDRAWN: A biphasic sessile mass of the buccal mucosa
    Tiffany M. Peters, Jose P. Zevallos, Brent A. Golden, Alice E. Curran
    Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology.2015;[Epub]     CrossRef
  • Mammary analogue secretory carcinoma: an evaluation of its clinicopathological and genetic characteristics
    Peter P. Luk, Christina I. Selinger, Timothy J. Eviston, Trina Lum, Bing Yu, Sandra A. O’Toole, Jonathan R. Clark, Ruta Gupta
    Pathology.2015; 47(7): 659.     CrossRef
  • A case of mammary analogue secretory carcinoma arising in the submandibular region
    Kotaro ISHII, Koji NAKAMATSU, Koji SATO, Chikashi MINEMURA, Wataru KUMAMARU, Hiroyo YOSHIKAWA
    Japanese Journal of Oral and Maxillofacial Surgery.2015; 61(11): 564.     CrossRef
  • DOG1, p63, and S100 protein: a novel immunohistochemical panel in the differential diagnosis of oncocytic salivary gland neoplasms in fine-needle aspiration cell blocks
    Alessandra C. Schmitt, Ryan McCormick, Cynthia Cohen, Momin T. Siddiqui
    Journal of the American Society of Cytopathology.2014; 3(6): 303.     CrossRef
  • Salivary Gland Tumor “Wishes” to Add to the Next WHO Tumor Classification: Sclerosing Polycystic Adenosis, Mammary Analogue Secretory Carcinoma, Cribriform Adenocarcinoma of the Tongue and Other Sites, and Mucinous Variant of Myoepithelioma
    Douglas R. Gnepp
    Head and Neck Pathology.2014; 8(1): 42.     CrossRef
  • Hepatoid differentiation in renal cell carcinoma: a rare histologic pattern with clinical significance
    Jungweon Shim, Heounjeong Go, Young-Suk Lim, Kyung Chul Moon, Jae Y. Ro, Yong Mee Cho
    Annals of Diagnostic Pathology.2014; 18(6): 363.     CrossRef
  • Mammary analogue secretory carcinoma: Update on a new diagnosis of salivary gland malignancy
    Roshan Sethi, Elliott Kozin, Aaron Remenschneider, Josh Meier, Paul VanderLaan, William Faquin, Daniel Deschler, Robert Frankenthaler
    The Laryngoscope.2014; 124(1): 188.     CrossRef
  • Mammary analog secretory carcinoma of salivary gland in a 5 year old: Case report
    Matthew Keisling, Michael Bianchi, Judy Mae Pascasio
    International Journal of Pediatric Otorhinolaryngology Extra.2014; 9(4): 163.     CrossRef
  • Fine-Needle Aspiration Cytology of Mammary Analog Secretory Carcinoma Masquerading as Low-Grade Mucoepidermoid Carcinoma: Case Report with a Review of the Literature
    Jaya Bajaj, Cecilia Gimenez, Farah Slim, Mohamed Aziz, Kasturi Das
    Acta Cytologica.2014; 58(5): 501.     CrossRef
Metastatic Carcinomas to the Oral Cavity and Oropharynx
Su-Jin Shin, Jong-Lyel Roh, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Sung Bae Kim, Sang-wook Lee, Kyung-Ja Cho
Korean J Pathol. 2012;46(3):266-271.   Published online June 22, 2012
DOI: https://doi.org/10.4132/KoreanJPathol.2012.46.3.266
  • 8,338 View
  • 66 Download
  • 17 Crossref
AbstractAbstract PDF
Background

Metastases to the oral/oropharynx are very rare and their diagnosis is challenging.

Methods

We reviewed pathologic data for malignant tumors of the oral/oropharynx that were diagnosed at the Asan Medical Center, Seoul, Korea from 1995 until 2010.

Results

Twenty-nine cases of oral/oropharyngeal metastases were retrieved, comprising 2.0% of 1,445 malignancies. The most common primary sites were the liver and lung, followed by the stomach, colon, breast, prostate, and kidney. The gingiva was the most common metastatic site, followed by the tonsil/pillar, mandible, tongue, tongue base, palate mucosa, mouth floor, and buccal mucosa. Intervals between detection of primary tumors and metastases were variable, from -1 month to 104 months. Ten patients with lung (7 cases), liver, stomach, and kidney carcinomas manifested with oral/oropharyngeal metastases as the first sign of systemic metastases. The majority of patients had died within one year of the onset of an oral/oropharyngeal metastasis, but exceptionally long-lived cases were also present. The survival periods of patients with lung cancers were longer than those of patients with non-pulmonary tumors.

Conclusions

An awareness of the incidence, common primary sites, metastatic subsites, and metastatic courses or patterns of oral/oropharyngeal metastases is helpful in the diagnosis of metastatic carcinomas.

Citations

Citations to this article as recorded by  
  • Metastasis of leiomyosarcoma to the sublingual region
    Seiji Baba, Kyoko Ishimaru, Eiji Ito, Saki Goto, Keizo Kato, Yoichi Yamada
    Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2024; 36(1): 95.     CrossRef
  • Mandibular metastasis of follicular thyroid carcinoma: A case report along with the concise review of literature
    MK Jawanda, R Narula, S Gupta, P Gupta
    Journal of Oral and Maxillofacial Pathology.2022; 26(1): 133.     CrossRef
  • Gingival metastasis from primary hepatocellular carcinoma: a case report
    Yuan Huang, Yanqiu Bao, Dongyuan Xu, Lan Liu
    Journal of International Medical Research.2022; 50(7): 030006052211134.     CrossRef
  • Lung carcinoma presenting as bilateral metastases in the mandibular gingivae: a case report and literature review
    Nusaybah Elsherif, Predrag Jeremic, Tim Blackburn
    Dental Update.2021; 48(10): 846.     CrossRef
  • Recurrent clear cell carcinoma of the tongue base with high grade transformation in a pregnant patient
    Emad M. Al Haj Ali, Ahmed M. Ibrahim, Tamer A. Ghanem, Christian E. Keller
    Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2020; 32(2): 104.     CrossRef
  • Primary Lingual Colonic-Type Adenocarcinoma: A Rare and Emerging Distinct Entity!
    Stephen M. Smith, Matthew Old, O. Hans Iwenofu
    Head and Neck Pathology.2017; 11(2): 234.     CrossRef
  • Rare Gingival Metastasis by Hepatocellular Carcinoma
    Li-Jun Xue, Xiao-Bei Mao, Jian Geng, Ya-Nan Chen, Qian Wang, Xiao-Yuan Chu
    Case Reports in Medicine.2017; 2017: 1.     CrossRef
  • Hepatoid adenocarcinoma of the lung metastasizing to the tonsil
    Luca Valle, Joel Thomas, Chul Kim, Eva Szabo, G. Thomas Brown, Deborah Citrin, Arun Rajan
    Molecular and Clinical Oncology.2017; 6(5): 705.     CrossRef
  • Epulis-Like Presentation of Gingival Renal Cancer Metastasis
    Gianfilippo Nifosì, Hubert Bressand, Antonio Fabrizio Nifosì, Lorenzo Nifosì, Pierre Damseaux
    Case Reports in Oncology.2017; 10(2): 758.     CrossRef
  • A Case of Oral Metastasis From Hepatocellular Carcinoma Displayed on 18F-FDG PET/CT Imaging
    Lei Jiang, Taoying Gu, Fang Liu, Lijuan Luan, Hongcheng Shi
    Clinical Nuclear Medicine.2016; 41(1): 72.     CrossRef
  • A case of renal cell carcinoma diagnosed in association with a palatal mucosa mass
    Masaharu NOI, Yoshizou TSUDA, Shota SAITO, Takeshi ADACHI, Tomoki HIGO, Gaku YAMAMOTO
    Japanese Journal of Oral and Maxillofacial Surgery.2016; 62(2): 62.     CrossRef
  • Unusual Presentation of an Adenocarcinoma of the Lung Metastasizing to the Mandible, Including Molecular Analysis and a Review of the Literature
    Sibel Elif Gultekin, Burcu Senguven, Ipek Isik Gonul, Begum Okur, Reinhard Buettner
    Journal of Oral and Maxillofacial Surgery.2016; 74(10): 2007.e1.     CrossRef
  • A Case of Hepatocellular Carcinoma Presenting as a Gingival Mass
    Min Jung Kwon, Soo Hyung Ryu, Soo Yeon Jo, Chul Hoon Kwak, Won Jae Yoon, Jeong Seop Moon, Hye Kyung Lee
    The Korean Journal of Gastroenterology.2016; 68(6): 321.     CrossRef
  • Mandibular metastasis of cholangiocarcinoma: A case report
    Tae Min You, Kee-Deog Kim, Ho-Gul Jeong, Wonse Park
    Imaging Science in Dentistry.2015; 45(4): 247.     CrossRef
  • Oral Floor and Gingival Metastasis of Cholangiocarcinoma: A Case Report and Review of the Literature
    Yukihiro Nakanishi, Bo Xu, Charles LeVea
    Case Reports in Pathology.2014; 2014: 1.     CrossRef
  • Primary Squamous Cell Carcinoma of Lung Leading to Metastatic Jaw Tumor
    Chintamaneni Raja Lakshmi, M. Sudhakara Rao, Sujana Mulk Bhavana, Sivan Sathish
    Case Reports in Pulmonology.2014; 2014: 1.     CrossRef
  • A Case of Gingival Metastasis from Rectal Cancer in Which Immunohistochemistry and PET-CT Were Useful for the Diagnostic Procedure
    Masami Yamauchi, Katsunori Shinozaki, Mihoko Doi, Tomoko Nitta, Takashi Nishisaka
    Case Reports in Oncology.2014; 7(1): 246.     CrossRef

J Pathol Transl Med : Journal of Pathology and Translational Medicine