Calcifying epithelial odontogenic tumors (CEOTs) and ghost cell odontogenic tumors (GCOTs) are characteristic odontogenic origin epithelial tumors which produce calcifying materials from transformed epithelial tumor cells. CEOT is a benign odontogenic tumor composed of polygonal epithelial tumor cells that show retrogressive calcific changes, amyloid-like deposition, and clear cytoplasm. Differentially, GCOTs are a group of transient tumors characterized by ghost cell presence, which comprise calcifying cystic odontogenic tumor (CCOT), dentinogenic ghost cell tumor (DGCT), and ghost cell odontogenic carcinoma (GCOC), all derived from calcifying odontogenic cysts (COCs). There is considerable confusion about COCs and GCOTs terminology, but these lesions can be classified as COCs or GCOTs, based on their cystic or tumorous natures, respectively. GCOTs include ameloblastomatous tumors derived from dominant odontogenic cysts classified as CCOTs, ghost cell-rich tumors producing dentinoid materials as DGCTs, and the GCOT malignant counterpart, GCOCs. Many authors have reported CEOTs and GCOTs variably express keratins, β-catenin, BCL-2, BSP, RANKL, OPG, Notch1, Jagged1, TGF-β, SMADs, and other proteins. However, these heterogeneous lesions should be differentially diagnosed to allow for accurate tumor progression and prognosis prediction.

Citations

Citations to this article as recorded by  

• A Calcifying Odontogenic Cyst With Compound Odontoma in the Maxillary Sinus: A Case Report in a Pediatric Patient
  Rodrigo A Oliveira, Ana C Maurício, Maria L Sacramento, Jorge Pinheiro, Mariana Moreira
  Cureus.2024;[Epub]     CrossRef
• A Current Review of Machine Learning and Deep Learning Models in Oral Cancer Diagnosis: Recent Technologies, Open Challenges, and Future Research Directions
  Shriniket Dixit, Anant Kumar, Kathiravan Srinivasan
  Diagnostics.2023; 13(7): 1353.     CrossRef
• Giant calcifying epithelial odontogenic tumor after I-125 seed implantation: A case report
  Yanchen Li, Kuo Wan, Mu Wang, Geping Cui, Bo Chen, Lijiang Yu, Yindong Liu, Haitao Dong, Zhihui Zhu, Ruiqi Zhao, Tao Zhang
  Heliyon.2023; 9(7): e17087.     CrossRef
• Calcifying odontogenic cyst mimicking odontogenic keratocyst: A diagnostic challenge
  Tanha Khan, Arpan Manna, MysoreK Sunil
  Amrita Journal of Medicine.2023; 19(3): 143.     CrossRef
• Calcifying epithelial odontogenic tumor- Review of literature
  Sivaramakrishnan Muthanandam, Akshitha Achuthan, A Santhadevy, Vezhavendhan N, Vidhyalakshmi, Umamaheswari G
  International Dental Journal of Student's Research.2023; 11(3): 103.     CrossRef
• Case report: Ghost cell odontogenic carcinoma in a dog: diagnostics and surgical outcome
  Chun-Geun Kim, Ga-Won Lee, Hyun Sil Kim, Seung-Yong Han, Dawool Han, Hee-Myung Park
  Frontiers in Veterinary Science.2023;[Epub]     CrossRef
• Immunohistochemical expression of Ki-67 and Glypican-3 to distinguish aggressive from nonaggressive benign odontogenic tumors
  TP Chaturvedi, Kanupriya Gupta, Rahul Agrawal, PG Naveen Kumar, Jatin Gupta
  Journal of Cancer Research and Therapeutics.2022; 18(9): 205.     CrossRef
• A novel parotid carcinoma with a prominent ghost cell population: a masquerading tumor or “salivary ghost cell carcinoma”?
  Hiroshi Harada, Mitsuo P. Sato, Naoki Otsuki, Mao Kawamura, Akira Kurose, Takao Satou
  Medical Molecular Morphology.2022; 55(1): 76.     CrossRef
• Ghost cells unveiled: A comprehensive review
  Aarushi Garg, Rewa Malhotra, Aadithya B. Urs
  Journal of Oral Biosciences.2022; 64(2): 202.     CrossRef
• Ghost Cell Odontogenic Carcinoma Arising in a Previous Calcifying Odontogenic Cyst: A Case Report and Review of Literature
  Ioana Ghita, Michael Y. Nagai, Joshua E. Lubek, Kristen M. Stashek, John R. Basile, Jeffery B. Price, John C. Papadimitriou, Donita Dyalram, Rania H. Younis
  Head and Neck Pathology.2022; 16(3): 828.     CrossRef
• Useful diagnostic histogenetic features of ectopic odontogenic ghost cell tumours
  Yuri Noda, Chisato Ohe, Mitsuaki Ishida, Kimiaki Okano, Kaori Sando, Naoya Hada, Yusuke Ebisu, Takuo Fujisawa, Masao Yagi, Hiroshi Iwai, Koji Tsuta
  BMC Oral Health.2022;[Epub]     CrossRef
• Histopathologic Feature of Hyalinization Predicts Recurrence of Conventional/Solid Multicystic Ameloblastomas
  Dominic Augustine, Roopa S. Rao, Lakshminarayana Surendra, Shankargouda Patil, Thuckanaickenpalayam Ragunathan Yoithapprabhunath, Sarah Albogami, Shaheen Shamsuddin, Sulphi Abdul Basheer, Shan Sainudeen
  Diagnostics.2022; 12(5): 1114.     CrossRef
• Multidisciplinary Case Management in Mesiodens Impacted Cases with Calcifying Odontogenic Cyst
  Tania Saskianti, Udijanto Tedjosaongko, Regina Ayu Pramudita, Nita Naomi, Alit Rahma Restu, Darko Macan
  Case Reports in Dentistry.2022; 2022: 1.     CrossRef
• Das Spektrum odontogener Zysten – ein Update
  S. Höller, N. Rupp
  Der MKG-Chirurg.2021; 14(2): 96.     CrossRef
• Dentinogenic Ghost Cell Tumor in a Sumatran Rhinoceros
  Annas Salleh, Zainal Z. Zainuddin, Reza M. M. Tarmizi, Chee K. Yap, Chian-Ren Jeng, Mohd Zamri-Saad
  Animals.2021; 11(4): 1173.     CrossRef
• GHOST CELLS UNDER MICROSCOPE: A PERPLEXED HYPOTHESIS
  Reema Raina, Nikita Gulati, Saurabh Juneja, Devi Charan Shetty
  INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH.2021; : 76.     CrossRef
• Ameloblastic fibro-odontoma in the mandible – Clinical, radiological and surgical aspect
  Divya Bharat, Jayesh Vahanwala, Ashok Dabir, Prachi Jobanputra
  Advances in Oral and Maxillofacial Surgery.2021; 2: 100066.     CrossRef
• Calcifying odontogenic cysts: A 20-year retrospective clinical and radiological review
  Chané Nel, Liam Robinson, Ana Luiza Oliveira Corrêa Roza, Pablo Agustin Vargas, Christoffel Johannes Nortjé, Willie FP van Heerden
  Dentomaxillofacial Radiology.2021; 50(6): 20200586.     CrossRef
• Case report and review of calcifying epithelial odontogenic tumor
  Jayarathi Ishwarya K S, V. Ramesh, P. D. Balamurali, Karthikshree V Prashad
  International Journal of Oral Health Dentistry.2021; 7(3): 206.     CrossRef
• Calcifying odontogenic cyst: A case report
  C. Mulvihill, S. Ni Mhaolcatha, P. Brady, J. McKenna, D. Sleeman, J. Fitzgibbon
  Oral Surgery.2020; 13(2): 177.     CrossRef
• Differential diagnosis of ameloblastic fibro-odontoma: case report and literature review
  Takayuki Kurimoto, Tadashi Yamanishi, Takeshi Harada, Keiko Matsuoka, Setsuko Uematsu, Yuri Yamamoto, Yuki Arimura, Takeshi Togawa, Naoko Inoue, Juntaro Nishio
  Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2019; 31(1): 38.     CrossRef
• Odontogenic Cysts and Tumors
  Dana Rioux-Forker, Allyson C. Deziel, Larry S. Williams, Arshad R. Muzaffar
  Annals of Plastic Surgery.2019; 82(4): 469.     CrossRef
• Perfil clínico e histopatológico do cisto odontogênico calcificante: relato de caso
  Hugo Leite Rodrigues Neto, Daniel Amaral Alves Marlière, Marcelo Galindo Silvares, Luciana Asprino, Rodrigo Alvitos Pereira
  HU Revista.2019; 43(4): 415.     CrossRef
• Ghost cell odontogenic carcinoma with suspected cholesterol granuloma of the maxillary sinus in a patient treated with combined modality therapy
  You Qin, Yanwei Lu, Liduan Zheng, Hong Liu
  Medicine.2018; 97(7): e9816.     CrossRef
• Calcifying odontogenic cyst, dentinogenic ghost cell tumor, and ghost cell odontogenic carcinoma: A systematic review
  José Alcides Almeida de Arruda, João Luiz Gomes Carneiro Monteiro, Lucas Guimarães Abreu, Leni Verônica de Oliveira Silva, Lauren Frenzel Schuch, Mariana Saturnino de Noronha, Gerhilde Callou, Amália Moreno, Ricardo Alves Mesquita
  Journal of Oral Pathology & Medicine.2018; 47(8): 721.     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
• Ghost Cell Tumors
  Jason Sheikh, Molly D. Cohen, Naomi Ramer, Ali Payami
  Journal of Oral and Maxillofacial Surgery.2017; 75(4): 750.     CrossRef
• Ghost cell odontogenic carcinoma on right mandible and its respective surgical reconstruction: a case report
  Sang Yoon Park, Joonhyoung Park, Do Hyun Kwon, Jae ho Jeon, Soung Min Kim, Hoon Myoung, Jong Ho Lee
  Journal of the Korean Association of Oral and Maxillofacial Surgeons.2017; 43(6): 415.     CrossRef
• Histologic Variants of Calcifying Odontogenic Cyst: A Study of 52 Cases
  Soussan Irani, Forough Foroughi
  The Journal of Contemporary Dental Practice.2017; 18(8): 688.     CrossRef
• Pediatric Odontogenic Cysts of the Jaws
  Kevin Arce, Christopher S. Streff, Kyle S. Ettinger
  Oral and Maxillofacial Surgery Clinics of North America.2016; 28(1): 21.     CrossRef
• Metastatic Ghost Cell Odontogenic Carcinoma: Description of a Case and Search for Actionable Targets
  Maximilien J. Rappaport, Darion L. Showell, William J. Edenfield
  Rare Tumors.2015; 7(3): 96.     CrossRef
• The Diagnostic Usefulness of Immunohistochemistry for Odontogenic Lesions
  Keith D. Hunter, Paul M. Speight
  Head and Neck Pathology.2014; 8(4): 392.     CrossRef

Citations

Citations to this article as recorded by  

• Lymphangioleiomyomatosis with Tuberous Sclerosis Complex—A Case Study
  Aleksandra Marciniak, Jolanta Nawrocka-Rutkowska, Agnieszka Brodowska, Andrzej Starczewski, Iwona Szydłowska
  Journal of Personalized Medicine.2023; 13(11): 1598.     CrossRef
• A case of lymphangioleiomyomatosis with endometrial cancer diagnosed by retroperitoneoscopic para-aortic lymph node dissection
  Aiko Ogasawara, Shogo Yamaguchi, Hiroaki Inui, Mieko Hanaoka, Daisuke Shintani, Sho Sato, Masanori Yasuda, Akira Yabuno
  JAPANESE JOURNAL OF GYNECOLOGIC AND OBSTETRIC ENDOSCOPY.2022; 38(1): 158.     CrossRef
• Primary retroperitoneal PEComa: an incidental finding
  Bárbara Monteiro Marinho, António Gâmboa Canha, Donzília Sousa Silva, José Davide Pinto Silva
  BMJ Case Reports.2022; 15(11): e250466.     CrossRef
• Imaging Findings of Thoracic Lymphatic Abnormalities
  Jingshuo (Derek) Sun, Thomas Shum, Fardad Behzadi, Mark M. Hammer
  RadioGraphics.2022; 42(5): 1265.     CrossRef
• Extrapulmonary uterine lymphangioleiomyomatosis (LAM) and dysfunctional uterine bleeding: the first presentation of LAM in a tuberous sclerosis complex patient
  Lucy Grant, Saliya Chipwete, San Soo Hoo, Anjali Bhatnagar
  BMJ Case Reports.2019; 12(2): e226358.     CrossRef
• Summary of the Japanese Respiratory Society statement for the treatment of lung cancer with comorbid interstitial pneumonia
  Takashi Ogura, Nagio Takigawa, Keisuke Tomii, Kazuma Kishi, Yoshikazu Inoue, Eiki Ichihara, Sakae Homma, Kazuhisa Takahashi, Hiroaki Akamatsu, Satoshi Ikeda, Naohiko Inase, Tae Iwasawa, Yuichiro Ohe, Hiromitsu Ohta, Hiroshi Onishi, Isamu Okamoto, Kazumasa
  Respiratory Investigation.2019; 57(6): 512.     CrossRef
• Incidental lymphangioleiomyomatosis in the lymph nodes of gynecologic surgical specimens
  Ikumi Kuno, Hiroshi Yoshida, Hanako Shimizu, Takashi Uehara, Masaya Uno, Mitsuya Ishikawa, Tomoyasu Kato
  European Journal of Obstetrics & Gynecology and Reproductive Biology.2018; 231: 93.     CrossRef
• Solitary extrapulmonary lymphangioleiomyomatosis of the liver: A case report and literature review
  Weiwei Fu, Yujun Li, Hong Li, Ping Yang, Xiaoming Xing
  Experimental and Therapeutic Medicine.2016; 12(3): 1499.     CrossRef
• Incidental Pelvic and Para-aortic Lymph Node Lymphangioleiomyomatosis Detected During Surgical Staging of Pelvic Cancer in Women Without Symptomatic Pulmonary Lymphangioleiomyomatosis or Tuberous Sclerosis Complex
  Joseph T. Rabban, Brandie Firetag, Ankur R. Sangoi, Miriam D. Post, Charles J. Zaloudek
  American Journal of Surgical Pathology.2015; 39(8): 1015.     CrossRef

Citations

Citations to this article as recorded by  

• Reference genes for gene expression profiling in mouse models of Listeria monocytogenes infection
  Lethicia Souza Tavares, Roberta Lane Oliveira-Silva, Marcelo Tigre Moura, Jéssica Barboza da Silva, Ana Maria Benko-Iseppon, José Vitor Lima-Filho
  BioTechniques.2024; 76(3): 104.     CrossRef
• Sarcolipin relates to fattening, but not sarco/endoplasmic reticulum Ca2+-ATPase uncoupling, in captive migratory gray catbirds
  Cory R. Elowe, Maria Stager, Alexander R. Gerson
  Journal of Experimental Biology.2024;[Epub]     CrossRef
• Assessment of the alpha 7 nicotinic acetylcholine receptor as an imaging marker of cardiac repair-associated processes using NS14490
  Victoria J. M. Reid, Wesley K. X. McLoughlin, Kalyani Pandya, Holly Stott, Monika Iškauskienė, Algirdas Šačkus, Judit A. Marti, Dominic Kurian, Thomas M. Wishart, Christophe Lucatelli, Dan Peters, Gillian A. Gray, Andrew H. Baker, David E. Newby, Patrick
  EJNMMI Research.2024;[Epub]     CrossRef
• Identification of differentially expressed genes at different post-natal development stages of longissimus dorsi muscle in Tianzhu white yak
  Bingang Shi, Xuehong Shi, Zhi Zuo, Shijie Zhao, Zhidong Zhao, Jiqing Wang, Huitong Zhou, Yuzhu Luo, Jiang Hu, Jon G.H. Hickford
  Gene.2022; 823: 146356.     CrossRef
• Specialized androgen synthesis in skeletal muscles that actuate elaborate social displays
  Eric R. Schuppe, Daniel Tobiansky, Franz Goller, Matthew J. Fuxjager
  Journal of Experimental Biology.2022;[Epub]     CrossRef
• Deep-ultraviolet laser ablation sampling for proteomic analysis of tissue
  Remilekun O. Lawal, Luke T. Richardson, Chao Dong, Fabrizio Donnarumma, Touradj Solouki, Kermit K. Murray
  Analytica Chimica Acta.2021; 1184: 339021.     CrossRef
• Protective effects of grape seed proanthocyanidins against iron overload-induced renal oxidative damage in rats
  Shaojun Yun, Dongyang Chu, Xingshuai He, Wenfang Zhang, Cuiping Feng
  Journal of Trace Elements in Medicine and Biology.2020; 57: 126407.     CrossRef
• Gene Expression Variation of Candidate Endogenous Control Genes Across Latitudinal Populations of the Bank Vole (Clethrionomys glareolus)
  Lucie Němcová, Silvia Marková, Petr Kotlík
  Frontiers in Ecology and Evolution.2020;[Epub]     CrossRef
• High-Fat Diet Alters the Expression of Reference Genes in Male Mice
  Xiuqin Fan, Hongyang Yao, Xuanyi Liu, Qiaoyu Shi, Liang Lv, Ping Li, Rui Wang, Tiantian Tang, Kemin Qi
  Frontiers in Nutrition.2020;[Epub]     CrossRef
• The applicability of forensic time since death estimation methods for buried bodies in advanced decomposition stages
  Stefan Pittner, Valentina Bugelli, M. Eric Benbow, Bianca Ehrenfellner, Angela Zissler, Carlo P. Campobasso, Roelof-Jan Oostra, Maurice C. G. Aalders, Richard Zehner, Lena Lutz, Fabio C. Monticelli, Christian Staufer, Katharina Helm, Vilma Pinchi, Joseph
  PLOS ONE.2020; 15(12): e0243395.     CrossRef
• Doublecortin-like Kinase 1 Regulates α-Synuclein Levels and Toxicity
  Gabriel E. Vázquez-Vélez, Kristyn A. Gonzales, Jean-Pierre Revelli, Carolyn J. Adamski, Fatemeh Alavi Naini, Aleksandar Bajić, Evelyn Craigen, Ronald Richman, Sabrina M. Heman-Ackah, Matthew J.A. Wood, Maxime W.C. Rousseaux, Huda Y. Zoghbi
  The Journal of Neuroscience.2020; 40(2): 459.     CrossRef
• The role of extracellular matrix stiffness in regulating cytoskeletal remodeling via vinculin in synthetic smooth muscle cells
  Kai Shen, Harshavardhan Kenche, Hua Zhao, Jinping Li, Jasimine Stone
  Biochemical and Biophysical Research Communications.2019; 508(1): 302.     CrossRef
• Combined proteomic and miRNome analyses of mouse testis exposed to an endocrine disruptors chemicals mixture reveals altered toxicological pathways involved in male infertility
  Julio Buñay, Eduardo Larriba, Daniel Patiño-Garcia, Paulina Urriola-Muñoz, Ricardo D Moreno, Jesús del Mazo
  MHR: Basic science of reproductive medicine.2019; 25(3): 156.     CrossRef
• Postmortem proteomics to discover biomarkers for forensic PMI estimation
  Kyoung-Min Choi, Angela Zissler, Eunjung Kim, Bianca Ehrenfellner, Eunji Cho, Se-in Lee, Peter Steinbacher, Ki Na Yun, Jong Hwan Shin, Jin Young Kim, Walter Stoiber, Heesun Chung, Fabio Carlo Monticelli, Jae-Young Kim, Stefan Pittner
  International Journal of Legal Medicine.2019; 133(3): 899.     CrossRef
• Aging‐associated changes in hippocampal glycogen metabolism in mice. Evidence for and against astrocyte‐to‐neuron lactate shuttle
  Dominika Drulis‐Fajdasz, Agnieszka Gizak, Tomasz Wójtowicz, Jacek R. Wiśniewski, Dariusz Rakus
  Glia.2018; 66(7): 1481.     CrossRef
• New insights into the distribution, protein abundance and subcellular localisation of the endogenous peroxisomal biogenesis proteins PEX3 and PEX19 in different organs and cell types of the adult mouse
  Claudia Colasante, Jiangping Chen, Barbara Ahlemeyer, Rocio Bonilla-Martinez, Srikanth Karnati, Eveline Baumgart-Vogt, Stephan N. Witt
  PLOS ONE.2017; 12(8): e0183150.     CrossRef
• Identification of valid endogenous control genes for determining gene expression in C6 glioma cell line treated with conditioned medium from adipose-derived stem cell
  I.C. Iser, R.P. de Campos, A.P.S. Bertoni, M.R. Wink
  Biomedicine & Pharmacotherapy.2015; 75: 75.     CrossRef
• Sclerosing Mucoepidermoid Carcinoma in the Parotid Gland: Literature Review
  Chang-Ki Woo, Bae-Hyun Kim, Byung-Joo Lee, Jin-Choon Lee
  Korean Journal of Otorhinolaryngology-Head and Neck Surgery.2012; 55(8): 508.     CrossRef

Citations

Citations to this article as recorded by  

• External validation of a deep learning-based algorithm for detection of tall cells in papillary thyroid carcinoma: A multicenter study
  Sebastian Stenman, Sylvain Bétrisey, Paula Vainio, Jutta Huvila, Mikael Lundin, Nina Linder, Anja Schmitt, Aurel Perren, Matthias S. Dettmer, Caj Haglund, Johanna Arola, Johan Lundin
  Journal of Pathology Informatics.2024; 15: 100366.     CrossRef
• Focal Tall Cell Change in Papillary Thyroid Carcinoma: Lessons Learned from Practices Adopting Rigid Criteria (Height to Width Ratio of 3)
  Esther Diana Rossi, Liron Pantanowitz
  Endocrine Pathology.2024; 35(1): 80.     CrossRef
• Papillary Thyroid Carcinomas with Tall Cell Features: An Intermediate Entity Between Classic and Tall Cell Subtypes
  Athanasios Bikas, Kristine Wong, Theodora Pappa, Sara Ahmadi, Craig B. Wakefield, Ellen Marqusee, Pingping Xiang, Benjamin Altshuler, Jacob Haase, Justine A. Barletta, Iñigo Landa, Erik K. Alexander
  Thyroid.2023; 33(6): 697.     CrossRef
• A novel nomogram for identifying high-risk patients among active surveillance candidates with papillary thyroid microcarcinoma
  Li Zhang, Peisong Wang, Kaixuan Li, Shuai Xue
  Frontiers in Endocrinology.2023;[Epub]     CrossRef
• The Impact of BRAF V600E Mutation Allele Frequency on the Histopathological Characteristics of Thyroid Cancer
  Mawaddah Abdulhaleem, Saruchi Bandargal, Marc Philippe Pusztaszeri, Mohannad Rajab, Hannah Greenspoon, Joshua Ross Krasner, Sabrina Daniela Da Silva, Véronique-Isabelle Forest, Richard J. Payne
  Cancers.2023; 16(1): 113.     CrossRef
• Protruding Huge Thyroid Mass Concurrent Hemorrhage and Skin Necrosis: A Case Report
  Solji An, Joonseon Park, Kwangsoon Kim, Ja Seong Bae, Jeong Soo Kim
  Journal of Endocrine Surgery.2023; 23(4): 143.     CrossRef
• CD56 Expression in Papillary Thyroid Carcinoma Is Highly Dependent on the Histologic Subtype: A Potential Diagnostic Pitfall
  Uiju Cho, Yourha Kim, Sora Jeon, Chan Kwon Jung
  Applied Immunohistochemistry & Molecular Morphology.2022; 30(5): 389.     CrossRef
• Aggressive histopathological variants of papillary thyroid carcinoma, diagnostic challenge, and clinical significance—A case series
  PK Pravanya, KR Anila, Shaji Thomas, A Sreekumar, K Jayasree
  Medical Journal of Dr. D.Y. Patil Vidyapeeth.2022;[Epub]     CrossRef
• Tall cell variant papillary thyroid carcinoma impacts disease-free survival at the 10 % cut-point on multivariate analysis
  Shabnam Samankan, Leah Militello, Gabriella Seo, Sedef Everest, Quinn O'Malley, Sarah L. Spaulding, Monica Xing, Ammar Matloob, John Beute, Raymond Chai, Scott Doyle, Mark L. Urken, Margaret Brandwein-Weber
  Pathology - Research and Practice.2022; 236: 154012.     CrossRef
• A population-based study of the three major variants of papillary thyroid carcinoma
  Junming Xu, Yingying Zhang, Jun Liu, Shenglong Qiu, Min Wang
  Journal of International Medical Research.2021; 49(2): 030006052098461.     CrossRef
• Tall cell percentage alone in PTC without aggressive features should not guide patients’ clinical management
  Anello Marcello Poma, David Viola, Elisabetta Macerola, Agnese Proietti, Eleonora Molinaro, Dario De Vietro, Rossella Elisei, Gabriele Materazzi, Paolo Miccoli, Fulvio Basolo, Clara Ugolini
  The Journal of Clinical Endocrinology & Metabolism.2021; 106(10): e4109.     CrossRef
• Molecular Pathology of Non-familial Follicular Epithelial–Derived Thyroid Cancer in Adults: From RAS/BRAF-like Tumor Designations to Molecular Risk Stratification
  Paula Soares, Antónia Afonso Póvoa, Miguel Melo, João Vinagre, Valdemar Máximo, Catarina Eloy, José Manuel Cameselle-Teijeiro, Manuel Sobrinho-Simões
  Endocrine Pathology.2021; 32(1): 44.     CrossRef
• Deep Neck Infection: Atypical Presentation of Papillary Thyroid Cancer
  Apichana Mahattanapreut, Rangsima Aroonroch, Chalermchai Chintrakarn, Chutintorn Sriphrapradang, Dinesh K. Chhetri
  Case Reports in Otolaryngology.2021; 2021: 1.     CrossRef
• The evolving concept of aggressive histological variants of differentiated thyroid cancer
  Juan C. Hernandez-Prera
  Seminars in Diagnostic Pathology.2020; 37(5): 228.     CrossRef
• Papillary Thyroid Cancer—Aggressive Variants and Impact on Management: A Narrative Review
  Andrés Coca-Pelaz, Jatin P. Shah, Juan C. Hernandez-Prera, Ronald A. Ghossein, Juan P. Rodrigo, Dana M. Hartl, Kerry D. Olsen, Ashok R. Shaha, Mark Zafereo, Carlos Suarez, Iain J. Nixon, Gregory W. Randolph, Antti A. Mäkitie, Luiz P. Kowalski, Vincent Van
  Advances in Therapy.2020; 37(7): 3112.     CrossRef
• Contemporary evaluation and management of tall cell variant of papillary thyroid carcinoma
  Sara Cartwright, Abbey Fingeret
  Current Opinion in Endocrinology, Diabetes & Obesity.2020; 27(5): 351.     CrossRef
• Le carcinome papillaire de la thyroïde avec contingent à cellules hautes : facteurs pronostiques
  I. Riahi, H. Jaafoura, H. Saibi, E. Chebil, I. Ben Nacef, M. Ksentini, T. Ben Ghachem, R. Lahiani, M. Ben Salah
  Annales d'Endocrinologie.2020; 81(4): 345.     CrossRef
• Updates in the Pathologic Classification of Thyroid Neoplasms: A Review of the World Health Organization Classification
  Yanhua Bai, Kennichi Kakudo, Chan Kwon Jung
  Endocrinology and Metabolism.2020; 35(4): 696.     CrossRef
• Tall Cell Variant of Papillary Thyroid Carcinoma: Impact of Change in WHO Definition and Molecular Analysis
  Kristine S. Wong, Sara E. Higgins, Ellen Marqusee, Matthew A. Nehs, Trevor Angell, Justine A. Barletta
  Endocrine Pathology.2019; 30(1): 43.     CrossRef
• Histopatological and molecular genetic characteristics of clinically aggressive variants of papillary thyroid carcinoma
  A. V. Bogolyubova, A. Yu. Abrosimov, L. S. Selivanova, P. V. Belousov
  Arkhiv patologii.2019; 81(1): 46.     CrossRef
• Papillary Thyroid Cancers with Focal Tall Cell Change are as Aggressive as Tall Cell Variants and Should Not be Considered as Low-Risk Disease
  Pim J. Bongers, Wouter P. Kluijfhout, Raoul Verzijl, Mattan Lustgarten, Marloes Vermeer, David P. Goldstein, Karen Devon, Lorne E. Rotstein, Sylvia L. Asa, James D. Brierley, Richard W. Tsang, Shereen Ezzat, Menno R. Vriens, Ozgur Mete, Jesse D. Pasternak
  Annals of Surgical Oncology.2019; 26(8): 2533.     CrossRef
• A case-based approach to aggressive variants of papillary thyroid carcinoma with literature review
  JosephAntoine Flordelis Chatto, AnnetteLaurente Salillas
  Thyroid Research and Practice.2019; 16(3): 128.     CrossRef
• Clinically Relevant Prognostic Parameters in Differentiated Thyroid Carcinoma
  Tyler Janovitz, Justine A. Barletta
  Endocrine Pathology.2018; 29(4): 357.     CrossRef
• Prediction of novel target genes and pathways involved in tall cell variant papillary thyroid carcinoma
  Fada Xia, Bo Jiang, Yong Chen, Xin Du, Yao Peng, Wenlong Wang, Zhuolu Wang, Xinying Li
  Medicine.2018; 97(51): e13802.     CrossRef
• Papillary thyroid carcinoma with tall cell features is as aggressive as tall cell variant: a meta-analysis
  Huy Gia Vuong, Nguyen Phuoc Long, Nguyen Hoang Anh, Tran Diem Nghi, Mai Van Hieu, Le Phi Hung, Tadao Nakazawa, Ryohei Katoh, Tetsuo Kondo
  Endocrine Connections.2018; 7(12): R286.     CrossRef
• TERT Promoter Mutation in an Aggressive Cribriform Morular Variant of Papillary Thyroid Carcinoma
  Eun Ji Oh, Sohee Lee, Ja Seong Bae, Yourha Kim, Sora Jeon, Chan Kwon Jung
  Endocrine Pathology.2017; 28(1): 49.     CrossRef
• Update on the cytologic features of papillary thyroid carcinoma variants
  Marc Pusztaszeri, Manon Auger
  Diagnostic Cytopathology.2017; 45(8): 714.     CrossRef
• Molecular correlates and rate of lymph node metastasis of non-invasive follicular thyroid neoplasm with papillary-like nuclear features and invasive follicular variant papillary thyroid carcinoma: the impact of rigid criteria to distinguish non-invasive f
  Uiju Cho, Ozgur Mete, Min-Hee Kim, Ja Seong Bae, Chan Kwon Jung
  Modern Pathology.2017; 30(6): 810.     CrossRef
• BRAF-positive paucicellular variant of anaplastic carcinoma in the presence of tall cell variant papillary thyroid cancer
  O. V. Dolzhansky, E. M. Paltseva, D. N. Khmelkova, F. A. Konovalov, I. V. Kanivets, A. V. Lavrov, D. V. Pyankov, S. A. Korostelev, O. A. Levendyuk, V. M. Pominalnaya, D. N. Fedorov
  Arkhiv patologii.2017; 79(3): 27.     CrossRef
• A comparison of the clinicopathological features and prognoses of the classical and the tall cell variant of papillary thyroid cancer: a meta-analysis
  Zeming Liu, Wen Zeng, Tianwen Chen, Yawen Guo, Chao Zhang, Chunping Liu, Tao Huang
  Oncotarget.2017; 8(4): 6222.     CrossRef
• Clinical utility of TERT promoter mutations and ALK rearrangement in thyroid cancer patients with a high prevalence of the BRAF V600E mutation
  Ja Seong Bae, Yourha Kim, Sora Jeon, Se Hee Kim, Tae Jung Kim, Sohee Lee, Min-Hee Kim, Dong Jun Lim, Youn Soo Lee, Chan Kwon Jung
  Diagnostic Pathology.2016;[Epub]     CrossRef
• Tall cell variant of papillary thyroid carcinoma: current evidence on clinicopathologic features and molecular biology
  Xiaofei Wang, Wenli Cheng, Chongqing Liu, Jingdong Li
  Oncotarget.2016; 7(26): 40792.     CrossRef
• The Warthin-Like Variant of Papillary Thyroid Carcinoma: A Comparison with Classic Type in the Patients with Coexisting Hashimoto’s Thyroiditis
  Min-kyung Yeo, Ja Seong Bae, Sohee Lee, Min-Hee Kim, Dong-Jun Lim, Youn Soo Lee, Chan Kwon Jung
  International Journal of Endocrinology.2015; 2015: 1.     CrossRef
• BRAF Immunohistochemistry Using Clone VE1 is Strongly Concordant with BRAFV600E Mutation Test in Papillary Thyroid Carcinoma
  Jung-Soo Pyo, Jin Hee Sohn, Guhyun Kang
  Endocrine Pathology.2015; 26(3): 211.     CrossRef
• Pathologie de la thyroïde. Cas no 3. Carcinome papillaire de la thyroïde, variante à cellules hautes
  Emmanuelle Leteurtre
  Annales de Pathologie.2015; 35(5): 402.     CrossRef

Citations

Citations to this article as recorded by  

• Cell Adhesion Molecule CD99 in Cancer Immunotherapy
  Feng Yu, Guodong Liu, Hailing Zhang, Xiaoyan Wang, Zhi Wu, Qinggang Xu, Yan Wu, Dongfeng Chen
  Current Molecular Medicine.2023; 23(10): 1028.     CrossRef
• Detection of Circulating Tumor Plasma Cells in Monoclonal Gammopathies: Methods, Pathogenic Role, and Clinical Implications
  Luzalba Sanoja-Flores, Juan Flores-Montero, Martín Pérez-Andrés, Noemí Puig, Alberto Orfao
  Cancers.2020; 12(6): 1499.     CrossRef
• Tumor suppressor CD99 is downregulated in plasma cell neoplasms lacking CCND1 translocation and distinguishes neoplastic from normal plasma cells and B-cell lymphomas with plasmacytic differentiation from primary plasma cell neoplasms
  Qi Gao, Venkata Yellapantula, Maly Fenelus, Janine Pichardo, Lu Wang, Ola Landgren, Ahmet Dogan, Mikhail Roshal
  Modern Pathology.2018; 31(6): 881.     CrossRef
• EWSR1 fusion proteins mediate PAX7 expression in Ewing sarcoma
  Gregory W Charville, Wei-Lien Wang, Davis R Ingram, Angshumoy Roy, Dafydd Thomas, Rajiv M Patel, Jason L Hornick, Matt van de Rijn, Alexander J Lazar
  Modern Pathology.2017; 30(9): 1312.     CrossRef
• Activation of the polycomb repressive complex pathway in the bone marrow resident cells of diffuse large B-cell lymphoma patients
  Eun Ji Oh, Eun Kyung Kim, Woo Ick Yang, Sun Och Yoon
  Leukemia & Lymphoma.2016; 57(8): 1921.     CrossRef
• CD99 Is Strongly Expressed in Basal Cells of the Normal Adult Epidermis and Some Subpopulations of Appendages: Comparison with Developing Fetal Skin
  Gawon Choi, Jin Roh, Chan-Sik Park
  Journal of Pathology and Translational Medicine.2016; 50(5): 361.     CrossRef
• Towards Stratified Medicine in Plasma Cell Myeloma
  Philip Egan, Stephen Drain, Caroline Conway, Anthony Bjourson, H. Alexander
  International Journal of Molecular Sciences.2016; 17(10): 1760.     CrossRef
• Human Myeloma Cell Lines Induce Osteoblast Downregulation of CD99 Which Is Involved in Osteoblast Formation and Activity
  Angela Oranger, Giacomina Brunetti, Claudia Carbone, Graziana Colaianni, Teresa Mongelli, Isabella Gigante, Roberto Tamma, Giorgio Mori, Adriana Di Benedetto, Marika Sciandra, Selena Ventura, Katia Scotlandi, Silvia Colucci, Maria Grano
  Journal of Immunology Research.2015; 2015: 1.     CrossRef
• CD99 regulates CXCL12-induced chemotaxis of human plasma cells
  Minchan Gil, Hyo-Kyung Pak, A-Neum Lee, Seo-Jung Park, Yoonkyung Lee, Jin Roh, Hyunji Lee, Yoo-Sam Chung, Chan-Sik Park
  Immunology Letters.2015; 168(2): 329.     CrossRef

Citations

Citations to this article as recorded by  

• Transition between canonical to non-canonical Wnt signaling during interactions between mesenchymal stem cells and osteosarcomas
  Asulin Masha, Ghedalia-Peled Noa Ben, Erez Ifat Cohen, Ventura Yvonne, Vago Razi
  Open Journal of Orthopedics and Rheumatology.2020; : 037.     CrossRef
• Mesenchymal stem-cell therapy for perianal fistulas in Crohn’s disease: a systematic review and meta-analysis
  F. Cheng, Z. Huang, Z. Li
  Techniques in Coloproctology.2019; 23(7): 613.     CrossRef
• Human mesenchymal stromal cells do not promote recurrence of soft tissue sarcomas in mouse xenografts after radiation and surgery
  PAOLA A. FILOMENO, KYUNG-PHIL KIM, NARA YOON, IRAN RASHEDI, VICTOR DAYAN, RITA A. KANDEL, XING-HUA WANG, TANIA C. FELIZARDO, ELLIOT BERINSTEIN, SALOMEH JELVEH, ANDREA FILOMENO, JEFFREY A. MEDIN, PETER C. FERGUSON, ARMAND KEATING
  Cytotherapy.2018; 20(8): 1001.     CrossRef
• Review article: mesenchymal stromal cell therapy for inflammatory bowel diseases
  C. Grégoire, C. Lechanteur, A. Briquet, É. Baudoux, F. Baron, E. Louis, Y. Beguin
  Alimentary Pharmacology & Therapeutics.2017; 45(2): 205.     CrossRef
• Effect of hGC-MSCs from human gastric cancer tissue on cell proliferation, invasion and epithelial-mesenchymal transition in tumor tissue of gastric cancer tumor-bearing mice
  Lin Song, Xin Zhou, Hong-Jun Jia, Mei Du, Jin-Ling Zhang, Liang Li
  Asian Pacific Journal of Tropical Medicine.2016; 9(8): 796.     CrossRef
• BMP9 inhibits the growth and migration of lung adenocarcinoma A549 cells in a bone marrow stromal cell-derived microenvironment through the MAPK/ERK and NF-κB pathways
  JING WANG, YAGUANG WENG, MINGHAO ZHANG, YA LI, MENGTIAN FAN, YANGLIU GUO, YANTING SUN, WANG LI, QIONG SHI
  Oncology Reports.2016; 36(1): 410.     CrossRef
• Comparative proteomic analysis of fibrosarcoma and skin fibroblast cell lines
  Ogunc Meral, Hamdi Uysal
  Tumor Biology.2015; 36(2): 561.     CrossRef
• Involvement of Wnt/β-catenin signaling in the mesenchymal stem cells promote metastatic growth and chemoresistance of cholangiocarcinoma
  Weiwei Wang, Wei Zhong, Jiahui Yuan, Congcong Yan, Shaoping Hu, Yinping Tong, Yubin Mao, Tianhui Hu, Bing Zhang, Gang Song
  Oncotarget.2015; 6(39): 42276.     CrossRef

Well-differentiated papillary mesothelioma is an uncommon tumor of the testes that usually presents as a hydrocele. Here, we present the case of one patient who did not have a history of asbestos exposure. The tumor was localized in the tunica vaginalis and was composed of three pedunculated masses macroscopically. Microscopically, branching papillary structures with focal coagulative necrosis were present. In addition to immunohistochemistry, simian virus 40 DNA was also tested by polymerase chain reaction. This report presents one case of this rare entity, its clinical and macroscopic features, and follow-up results.

Citations

Citations to this article as recorded by  

• Testicular/paratesticular mesothelial tumours: Uncommon histopathologic entities in a very complex anatomical site
  Francesca Pagliuca, Stefano Lucà, Marco De Sio, Davide Arcaniolo, Gaetano Facchini, Marco De Martino, Francesco Esposito, Ferdinando DE Vita, Paolo Chieffi, Renato Franco
  Pathology - Research and Practice.2024; 253: 155069.     CrossRef
• Well-differentiated Papillary Mesothelial Tumour of the Tunica Vaginalis Testis – A Rare Lesion, but one Pathologists Should Know About Two Patient Reports and a Review of the Literature
  Johannes Kläger, Felicitas Oberndorfer, Cristophe Brunel, Julian Veser, Eva Compérat
  International Journal of Surgical Pathology.2023; 31(6): 1126.     CrossRef
• A diagnostic approach to paratesticular lesions with tubulopapillary architecture: a series of 16 serous borderline tumors/low-grade serous carcinoma and 14 well-differentiated papillary mesothelial tumors and mesothelioma
  Rabia Zafar, Lacey J. Schrader, John C. Cheville, J. Kenneth Schoolmeester, Anja C. Roden, Marie-Christine Aubry, Eunhee S. Yi, Aditya Raghunathan, Loren Herrera-Hernandez, R. Houston Thompson, Stephen A. Boorjian, Bradley C. Leibovich, Gary L. Keeney, Ra
  Human Pathology.2022; 128: 31.     CrossRef
• Mesothelioma subtypes of the tunica vaginalis: a rare case report and review of histological criteria
  Cutts Rebecca, Martin J Connor, Luxi Sun, Thomas Johnston, Rachel Gooch, John McLoughlin
  Journal of Surgical Case Reports.2019;[Epub]     CrossRef
• Well‐differentiated papillary mesothelioma of tunica vaginalis testis of unknown malignant potential: Sonographic appearance
  K.W.S. Ko, K.S. Tse, K.W. Shek, M.N. Hau, S.H. Ting
  Journal of Clinical Ultrasound.2018; 46(5): 364.     CrossRef
• Tunica Vaginalis Thickening, Hemorrhagic Infiltration and Inflammatory Changes in 8 Children with Primary Hydrocele; Reactive Mesothelial Hyperplasia? A Prospective Clinical Study
  Ioannis Patoulias, Evangelia Rachmani, Maria Kalogirou, Kyriakos Chatzopoulos, Dimitrios Patoulias
  Acta Medica (Hradec Kralove, Czech Republic).2018; 61(2): 41.     CrossRef
• A 45-year-old man presenting with chest pain
  Sheetu Singh, Arpita Jindal
  Lung India.2018; 35(2): 171.     CrossRef
• Two Case Reports of Benign Testicular Mesothelioma and Review of the Literature
  Cristobal Ramirez Sevilla, Carme Admella Salvador, Josep Feliu Canaleta, Juan Llopis Manzanera, Miguel Angel Barranco Sanz, Juan Antoni Romero Martin, Sergi Bernal Salguero
  Case Reports in Oncological Medicine.2017; 2017: 1.     CrossRef
• Well-differentiated Papillary Mesothelioma of the Tunica Vaginalis
  Wei Keith Tan, Mae-Yen Tan, Hui Meng Tan, Rajadurai Pathmanathan, Wei Phin Tan
  Urology.2016; 90: e7.     CrossRef
• Well-Differentiated Papillary Mesothelioma of the Tunica Vaginalis: Case Report and Systematic Review of Literature
  Wei Keith Tan, Mae-Yen Tan, Wei Shen Tan, Soon Ching Gan, Rajadurai Pathmanathan, Hui Meng Tan, Wei Phin Tan
  Clinical Genitourinary Cancer.2016; 14(4): e435.     CrossRef
• The legacy of the F344 rat as a cancer bioassay model (a retrospective summary of three common F344 rat neoplasms)
  Robert R. Maronpot, Abraham Nyska, Jennifer E. Foreman, Yuval Ramot
  Critical Reviews in Toxicology.2016; 46(8): 641.     CrossRef
• Malignant Mesothelioma of the Tunica Vaginalis: A Rare Neoplasm—Case Report and Literature Review
  Manuel Segura-González, Jorge Urias-Rocha, Jorge Castelán-Pedraza
  Clinical Genitourinary Cancer.2015; 13(6): e401.     CrossRef
• In vivo Optical Coherence Tomography Imaging of the Mesothelium Using Developed Window Models
  Yeh-Chan Ahn, Yu-Gyeong Chae, Sang Seok Hwang, Bong-Kwon Chun, Maan Hong Jung, Sung Jin Nam, Hae-Young Lee, Jae Min Chung, Chulho Oak, Eun-Kee Park
  Journal of the Optical Society of Korea.2015; 19(1): 69.     CrossRef

This paper reports a case of low-grade adenosquamous carcinoma (LGASC) arising in a 69-year-old woman, who presented with a 1-cm palpable mass on her right breast. Core needle biopsy diagnosed the mass as a fibroadenoma. After six months, the mass increased in size, and the patient received subsequent mammotome excision. On microscopic examination, bland-looking small glands were infiltrating into the fibrotic stroma with lymphocytic infiltrates at the periphery. Hematoxylin and eosin staining revealed relatively easily detectable myoepithelial cells along the outside in each of the glandular structures with variable degrees of squamous metaplasia. Based on histologic features, the patient was diagnosed with LGASC. LGASC is a rare variant of metaplastic carcinoma, which is characterized by a favorable prognosis. Due to the bland cytology and presence of myoepithelial cells, LGASC can be misdiagnosed as benign lesion. Additionally, inconsistent expression of myoepithelial markers could aid the diagnosis of LGASC.

Citations

Citations to this article as recorded by  

• High rate of PIK3CA mutations but no TP53 mutations in low‐grade adenosquamous carcinoma of the breast
  Guillaume Bataillon, Laetitia Fuhrmann, Elodie Girard, Emanuelle Menet, Marick Laé, Mathieu Capovilla, Isabelle Treilleux, Laurent Arnould, Frederique Penault‐Llorca, Roman Rouzier, Caterina Marchiò, Ivan Bieche, Anne Vincent‐Salomon
  Histopathology.2018; 73(2): 273.     CrossRef
• Low-grade Adenosquamous Carcinoma Coexisting with Sclerosing Adenosis of the Breast: A Case Report
  Ryoko Oi, Ichiro Maeda, Yoshio Aida, Yukari Yabuki, Toru Nishikawa, Yoshihide Kanemaki, Koichiro Tsugawa, Masayuki Takagi
  Journal of St. Marianna University.2017; 8(1): 31.     CrossRef
• Low-grade Adenosquamous Carcinoma of the Breast
  Haruko SAKAMOTO, Akihiko SHIMANA, Hideaki HORI, Kouki TOKUDA, Hitoshi TSUBOUCHI, Miki TAKENAKA, Rin YAMAGUCHI
  Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2017; 78(9): 1983.     CrossRef
• Small Glandular Proliferations of the Breast With Absent or Attenuated Myoepithelial Reactivity by Immunohistochemistry: A Review Focusing on the Differential Diagnosis and Interpretative Pitfalls
  Paula S. Ginter, Sandra J. Shin, Timothy M. D'Alfonso
  Archives of Pathology & Laboratory Medicine.2016; 140(7): 651.     CrossRef
• Bilateral synchronous low-grade adenosquamous carcinoma of the breast: A Case report with review of the current literature
  J.L. Senger, P. Meiers, R. Kanthan
  International Journal of Surgery Case Reports.2015; 14: 53.     CrossRef
• A Nation-Wide Cancer Registry-Based Study of Adenosquamous Carcinoma in Taiwan
  Yuan-Tzu Lan, Kuo-Hung Huang, Chien-An Liu, Ling-Chen Tai, Ming-Huang Chen, Yee Chao, Anna Fen-Yau Li, Shih-Hwa Chiou, Yi-Ming Shyr, Chew-Wun Wu, Wen-Liang Fang, Sheng-Nan Lu
  PLOS ONE.2015; 10(10): e0139748.     CrossRef

This study reports a case of anaplastic transformation from a well-differentiated thyroid carcinoma in a young patient. The first recurrent tissue contained poorly differentiated foci that revealed lower thyroglobulin, thyroid transcription factor 1 (TTF-1), and galectin-3 expression than the well-differentiated area. However there was no increased p53 or Ki-67 expression in the poorly differentiated foci, nor in the well-differentiated area. The tissue subsequently relapsed and revealed only anaplastic features, complete loss of thyroglobulin, TTF-1, and galectin-3 expression and revealed an increase in p53 and Ki-67 expression. The BRAF V600E and BRAF V600V mutation were found in the initially diagnosed papillary thyroid carcinoma and the poorly differentiated foci of the recurring papillary thyroid carcinoma; however, only the BRAF V600V mutation was found in the anaplastic carcinoma. These results suggest that overexpression of p53 and Ki-67 contributed to the anaplastic transformation. We also found that the BRAF type changed during the tumor relapse.

Citations

Citations to this article as recorded by  

• Immunomodulation exerted by galectins: a land of opportunity in rare cancers
  Laura Díaz-Alvarez, Georgina I. López-Cortés, Erandi Pérez-Figueroa
  Frontiers in Immunology.2023;[Epub]     CrossRef
• Coexisting well-differentiated and anaplastic thyroid carcinoma in the same primary resection specimen: immunophenotypic and genetic comparison of the two components in a consecutive series of 13 cases and a review of the literature
  Moira Ragazzi, Federica Torricelli, Benedetta Donati, Alessia Ciarrocchi, Dario de Biase, Giovanni Tallini, Eleonora Zanetti, Alessandra Bisagni, Elisabetta Kuhn, Davide Giordano, Andrea Frasoldati, Simonetta Piana
  Virchows Archiv.2021; 478(2): 265.     CrossRef
• HDAC Inhibition Induces PD-L1 Expression in a Novel Anaplastic Thyroid Cancer Cell Line
  Luca Hegedűs, Dominika Rittler, Tamás Garay, Paul Stockhammer, Ildikó Kovács, Balázs Döme, Sarah Theurer, Thomas Hager, Thomas Herold, Stavros Kalbourtzis, Agnes Bankfalvi, Kurt W. Schmid, Dagmar Führer, Clemens Aigner, Balázs Hegedűs
  Pathology & Oncology Research.2020; 26(4): 2523.     CrossRef
• EWSR1 rearrangement is a frequent event in papillary thyroid carcinoma and in carcinoma of the thyroid with Ewing family tumor elements (CEFTE)
  G. Oliveira, A. Polónia, J. M. Cameselle-Teijeiro, D. Leitão, S. Sapia, M. Sobrinho-Simões, C. Eloy
  Virchows Archiv.2017; 470(5): 517.     CrossRef
• Anaplastic carcinoma of the thyroid in a 12-year old girl
  Rodrigo Mon, James Newlon
  Journal of Pediatric Surgery Case Reports.2015; 3(9): 404.     CrossRef

Angiosarcoma with predominantly epithelioid features is a rare soft tissue neoplasm and the interpretation of its cytopathologic findings may be difficult. We report a case of metastatic angiosarcoma with predominantly epithelioid features diagnosed by liquid-based cytology. The cytopathologic findings in this case differed from those of the conventional preparation and we found a clean background, no hyperchromatic nuclei and several cytoplasmic changes, including intracytoplasmic vacuoles with peculiar shapes, juxtanuclear condensation and perinuclear clearing. Identification of these changes using liquid-based cytology supplemented with immunochemistry may be helpful in reaching a correct cytopathologic diagnosis.

Citations

Citations to this article as recorded by  

• Cytological Features of a Metastatic Angiosarcoma in the Lymph Node Diagnosed via Liquid-Based Cytology
  Jie-Yang Jhuang, Chih-Yi Liu, Min-Hui Tseng, Shih-Sung Chuang
  Diagnostics.2023; 13(12): 2124.     CrossRef
• Radiation-associated Angiosarcoma Presenting as Massive Pleural Effusion
  Hirokazu Ogino, Makoto Tobiume, Kozo Kagawa, Hiroshi Kawano, Satoshi Sakaguchi, Atsuro Saijo, Daisuke Matsumoto, Hiromitsu Takizawa, Yuriko Morikawa, Yoshimi Bando, Hisatsugu Goto, Hiroshi Nokihara, Yasuhiko Nishioka
  Internal Medicine.2022; 61(9): 1393.     CrossRef
• Delayed diagnosis of angiosarcoma of the spleen: clinically presenting as recurrent haemoperitoneum following embolisation
  V. Kornmann, P. van Rijn, D. Mulder, K. Reijnders
  Case Reports.2015; 2015(apr09 1): bcr2014208956.     CrossRef
• A Case of Angiosarcoma of the Scalp with Invasion to the Pleural Effusion
  Yusuke Amano, Yukari Obana, Yoko Nakanishi, Ryusuke Tsujimura, Kayomi Wakamatsu, Fumiko Uemura, Yoshihisa Katsura, Masahiko Sugitani, Norimichi Nemoto
  Journal of Nihon University Medical Association.2015; 74(3): 113.     CrossRef

Citations

Citations to this article as recorded by  

• Bilateral Stafne Bone Cavity in the Body of the Mandible: An Unusual Case Report and Literature Review
  Mayank Pahadia, Rutvi Vyas
  Cureus.2023;[Epub]     CrossRef
• Effect of Stafne bone defect on the adjacent tooth: A review of the literature
  Mahdi Niknami, Azin Parsa, Zahra Khodadadi
  Imaging Science in Dentistry.2022; 52(2): 165.     CrossRef
• Assessment of prevalence and volumetric estimation of possible Stafne bone concavities on cone beam computed tomography images
  Alaettin Koç, Cennet Neslihan Eroğlu, Ersen Bilgili
  Oral Radiology.2020; 36(3): 254.     CrossRef
• Stafne’s bone cyst revisited and renamed: the benign mandibular concavity
  Johan K.M. Aps, Natasha Koelmeyer, Cina Yaqub
  Dentomaxillofacial Radiology.2020; 49(4): 20190475.     CrossRef
• Cone‐beam computed tomography analysis of lingual mandibular bone depression in the premolar region: A case report
  Saeed Asgary, Naghmeh Emadi
  Clinical Case Reports.2020; 8(3): 523.     CrossRef
• Letters to the Editor
  Ariyan S Araghi, Richard M Graham
  Dental Update.2019; 46(8): 792.     CrossRef
• Radiographic features of lingual mandibular bone depression using dental cone beam computed tomography
  Liu Liu, Byung Cheol Kang, Suk Ja Yoon, Jae Seo Lee, Sel Ae Hwang
  Dentomaxillofacial Radiology.2018; 47(6): 20170383.     CrossRef
• Stafne's bone cavity – unusual presentation in the anterior mandible
  Ioan Davies, Holly Boyes, James Wykes, Graham Smith
  Dental Update.2018; 45(4): 340.     CrossRef
• Anterior stafne bone cyst mimicking periapical cyst: a case report
  Ji-Young Song
  Journal of Dental Rehabilitation and Applied Science.2016; 32(3): 209.     CrossRef

Citations

Citations to this article as recorded by  

• A case of slow-growing dedifferentiated solitary fibrous tumor of the pleura over a 7-year period
  Madoka Goto, Rio Takada, Yasuhisa Ichikawa, Hideki Tsubouchi, Yuta Kawasumi, Shoichi Mori
  The Journal of the Japanese Association for Chest Surgery.2022; 36(7): 821.     CrossRef
• A Comprehensive Review on Solitary Fibrous Tumor: New Insights for New Horizons
  Javier Martin-Broto, Jose L. Mondaza-Hernandez, David S. Moura, Nadia Hindi
  Cancers.2021; 13(12): 2913.     CrossRef
• An intrathoracic giant tumour and vanishing lung cyst after tumour resection
  Masashi Nishimura, Shinichiro Ota, Sumitaka Yamanaka, Kanako Shinada, Masaharu Shinkai
  Respirology Case Reports.2021;[Epub]     CrossRef
• Molecular changes in solitary fibrous tumor progression
  Hyung Kyu Park, Dan Bi Yu, Minjung Sung, Ensel Oh, Mingi Kim, Ji-Young Song, Mi-Sook Lee, Kyungsoo Jung, Ka-Won Noh, Sungbin An, Kyoung Song, Do-Hyun Nam, Yu Jin Kim, Yoon-La Choi
  Journal of Molecular Medicine.2019; 97(10): 1413.     CrossRef
• A Case Report of Solitary Fibrous Tumor in the Axilla of a 4-year-old Girl with Additional Marker Chromosome
  Ji Hye Park, Eun Jeong Kim, O Kyu Noh, Hyun Ju Jung, Jun Eun Park
  Clinical Pediatric Hematology-Oncology.2015; 22(2): 171.     CrossRef

Citations

Citations to this article as recorded by  

• Giant supra and retrosellar glioependymal cyst presenting with only precocious puberty. Clinical study and review of the literature
  Hassan Kadri, Mazen Dughly, Mohamad Shehadeh Agha, Ghiath Hamed, Raed Abouharb, Rostom Mackieh
  International Journal of Surgery Case Reports.2024; 116: 109360.     CrossRef
• Combined neuroendoscopic cyst wall fenestration and cyst-peritoneal shunt in an infant with glioependymal cyst
  Kohei Irie, Takafumi Shimogawa, Nobutaka Mukae, Daisuke Kuga, Toru Iwaki, Masahiro Mizoguchi, Koji Yoshimoto
  Surgical Neurology International.2022; 13: 102.     CrossRef
• Cerebellar Glioependymal Cyst
  El Kim
  Brain Tumor Research and Treatment.2021; 9(1): 31.     CrossRef
• Intracranial glioependymal (neuroglial) cysts: a systematic review
  Luis A. Robles, Jesus M. Paez, Dafne Ayala, Bernardo Boleaga-Duran
  Acta Neurochirurgica.2018; 160(7): 1439.     CrossRef

Citations

Citations to this article as recorded by  

• Small bowel and lung histiocytic sarcoma revealed by acute peritonitis: A case report with review of literature
  Ahlem Bellalah, Ibtissem korbi, Seifeddine Ben Hammouda, Asma Achour, Nouha Ben Abdeljelil, Manel Njima, Amira Daldoul, Rim Hadhri, Leila Njim, Abdelfatteh Zakhama
  Annals of Medicine and Surgery.2021; 68: 102638.     CrossRef
• An unexpected diagnosis of histiocytic sarcoma
  Joshua T. Byers, Samuel W. French
  Experimental and Molecular Pathology.2019; 106: 60.     CrossRef
• NLRX1 suppresses tumorigenesis and attenuates histiocytic sarcoma through the negative regulation of NF-λB signaling
  Sheryl Coutermarsh-Ott, Alysha Simmons, Vittoria Capria, Tanya LeRoith, Justin E. Wilson, Bettina Heid, Casandra W. Philipson, Qizhi Qin, Raquel Hontecillas-Magarzo, Josep Bassaganya-Riera, Jenny P-Y Ting, Nikolaos Dervisis, Irving C. Allen
  Oncotarget.2016; 7(22): 33096.     CrossRef