Literature DB >> 30349028

Diagnostic accuracy of a panel of immunohistochemical and molecular markers to distinguish Merkel cell carcinoma from other neuroendocrine carcinomas.

Thibault Kervarrec1,2,3, Anne Tallet4, Elodie Miquelestorena-Standley1, Roland Houben3, David Schrama3, Thilo Gambichler5, Patricia Berthon2, Yannick Le Corre6, Ewa Hainaut-Wierzbicka7, Francois Aubin8, Guido Bens9, Flore Tabareau-Delalande10, Nathalie Beneton11, Gaëlle Fromont12, Flavie Arbion12, Emmanuelle Leteurtre13, Antoine Touzé2, Mahtab Samimi2,14, Serge Guyétant15,16.   

Abstract

Merkel cell carcinoma is a rare neuroendocrine carcinoma of the skin mostly induced by Merkel cell polyomavirus integration. Cytokeratin 20 (CK20) positivity is currently used to distinguish Merkel cell carcinomas from other neuroendocrine carcinomas. However, this distinction may be challenging in CK20-negative cases and in cases without a primary skin tumor. The objectives of this study were first to evaluate the diagnostic accuracy of previously described markers for the diagnosis of Merkel cell carcinoma and second to validate these markers in the setting of difficult-to-diagnose Merkel cell carcinoma variants. In a preliminary set (n = 30), we assessed optimal immunohistochemical patterns (CK20, thyroid transcription factor 1 [TTF-1], atonal homolog 1 [ATOH1], neurofilament [NF], special AT-rich sequence-binding protein 2 [SATB2], paired box protein 5, terminal desoxynucleotidyl transferase, CD99, mucin 1, and Merkel cell polyomavirus-large T antigen) and Merkel cell polyomavirus load thresholds (real-time PCR). The diagnostic accuracy of each marker was then assessed in a validation set of 103 Merkel cell carcinomas (9 CK20-negative cases and 15 cases without a primary skin tumor) and 70 extracutaneous neuroendocrine carcinoma cases. The most discriminant markers for a diagnosis of Merkel cell carcinoma were SATB2, NF expression, and Merkel cell polyomavirus DNA detection (positive likelihood ratios: 36.6, 44.4, and 28.2, respectively). Regarding Merkel cell carcinoma variants, cases without a primary skin tumor retained a similar immunohistochemical  profile and CK20-negative tumors displayed a different profile (decrease frequency of NF and SATB2 expression), but Merkel cell polyomavirus DNA remained detected (78% of cases by qPCR). Moreover, 8/9 (89%) CK20-negative Merkel cell carcinoma cases but only 3/61 (5%) CK20-negative extracutaneous neuroendocrine cases were positive for at least one of these markers. In conclusion, detection of SATB2 and NF expression and Merkel cell polyomavirus DNA helps distinguish between Merkel cell carcinoma classical and variant cases and extracutaneous neuroendocrine carcinomas.

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Year:  2018        PMID: 30349028     DOI: 10.1038/s41379-018-0155-y

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  11 in total

1.  SATB2 in neuroendocrine neoplasms: strong expression is restricted to well-differentiated tumours of lower gastrointestinal tract origin and is most frequent in Merkel cell carcinoma among poorly differentiated carcinomas.

Authors:  Andrew M Bellizzi
Journal:  Histopathology       Date:  2019-11-15       Impact factor: 5.087

Review 2.  Merkel cell carcinoma of the anorectum: a case report and review of the literature.

Authors:  Abraham C van Wyk; Zaheer Moolla; Ahmed I Motala; Riyaadh Roberts; Nivesh A Chotey; Hoosen I Lakhi; Jürgen C Becker
Journal:  Clin J Gastroenterol       Date:  2022-06-28

Review 3.  Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Overview of the 2022 WHO Classification of Head and Neck Neuroendocrine Neoplasms.

Authors:  Ozgur Mete; Bruce M Wenig
Journal:  Head Neck Pathol       Date:  2022-03-21

4.  Merkel cell carcinoma of the eyelid and periocular region: A review.

Authors:  Noreen M Walsh
Journal:  Saudi J Ophthalmol       Date:  2022-04-18

Review 5.  An update on the development of concepts, diagnostic criteria, and challenging issues for neuroendocrine neoplasms across different digestive organs.

Authors:  Anne Couvelard; Jérôme Cros
Journal:  Virchows Arch       Date:  2022-03-12       Impact factor: 4.064

6.  Merkel cell polyomavirus is implicated in a subset of Merkel cell carcinomas, in the Indian subcontinent.

Authors:  Reety Arora; Bharat Rekhi; Pratik Chandrani; Sudhir Krishna; Amit Dutt
Journal:  Microb Pathog       Date:  2019-10-07       Impact factor: 3.738

7.  Characterizing DNA methylation signatures and their potential functional roles in Merkel cell carcinoma.

Authors:  Hemant Gujar; Arjun Mehta; Hong-Tao Li; Yvonne C Tsai; Xiangning Qiu; Daniel J Weisenberger; Miriam Galvonas Jasiulionis; Gino K In; Gangning Liang
Journal:  Genome Med       Date:  2021-08-16       Impact factor: 11.117

8.  Transcription Factor Expression in Sinonasal Neuroendocrine Neoplasms and Olfactory Neuroblastoma (ONB): Hyams' Grades 1-3 ONBs Expand the Spectrum of SATB2 and GATA3-Positive Neoplasms.

Authors:  Silvia Uccella; Carla Facco; Anna Maria Chiaravalli; Fabiana Pettenon; Stefano La Rosa; Mario Turri-Zanoni; Paolo Castelnuovo; Michele Cerati; Fausto Sessa
Journal:  Endocr Pathol       Date:  2022-05-06       Impact factor: 4.056

Review 9.  An Algorithmic Immunohistochemical Approach to Define Tumor Type and Assign Site of Origin.

Authors:  Andrew M Bellizzi
Journal:  Adv Anat Pathol       Date:  2020-05       Impact factor: 4.571

10.  Merkel cell carcinoma presenting as a malignant pleural effusion post-COVID-19 hospitalization: A case report and literature review.

Authors:  Joel Lanceta; Mesut Toprak; Oana C Rosca
Journal:  Diagn Cytopathol       Date:  2021-10-05       Impact factor: 1.582

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