S2k Guideline – Merkel cell carcinoma (MCC, neuroendocrine carcinoma of the skin) – Update 2022

Summary Merkel cell carcinoma (MCC, ICD‐O M8247/3) is a rare, malignant, primary skin tumor with epithelial and neuroendocrine differentiation. The tumor cells share many morphologic, immunohistochemical, and ultrastructural features with cutaneous Merkel cells. Nevertheless, the cell of origin of M...

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Published inJournal der Deutschen Dermatologischen Gesellschaft Vol. 21; no. 3; pp. 305 - 320
Main Authors Becker, Jürgen C., Beer, Ambros J., DeTemple, Viola K., Eigentler, Thomas, Flaig, Michael, Gambichler, Thilo, Grabbe, Stephan, Höller, Ulrike, Klumpp, Bernhard, Lang, Stephan, Pföhler, Claudia, Posch, Christian, Prasad, Vikas, Schlattmann, Peter, Schneider‐Burrus, Sylke, Ter‐Nedden, Jan, Terheyden, Patrick, Thoms, Kai, Vordermark, Dirk, Ugurel, Selma
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.03.2023
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ISSN1610-0379
1610-0387
1610-0387
DOI10.1111/ddg.14930

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Summary:Summary Merkel cell carcinoma (MCC, ICD‐O M8247/3) is a rare, malignant, primary skin tumor with epithelial and neuroendocrine differentiation. The tumor cells share many morphologic, immunohistochemical, and ultrastructural features with cutaneous Merkel cells. Nevertheless, the cell of origin of MCC is unclear. MCC appears clinically as a reddish to purple spherical tumor with a smooth, shiny surface and a soft to turgid, elastic consistency, usually showing rapid growth. Spontaneous and often complete regressions of the tumor are observed. These likely immunologically‐mediated regressions explain the cases in which only lymph node or distant metastases are found at the time of initial diagnosis and why the tumor responds very well to immunomodulatory therapies even at advanced stages. Due to its aggressiveness, the usually given indication for sentinel lymph node biopsy, the indication of adjuvant therapies to be evaluated, as well as the complexity of the necessary diagnostics, clinical management should already be determined by an interdisciplinary tumor board at the time of initial diagnosis.
Bibliography:This guideline has been updated from the S2k guideline published in 2018. Sections that did not require updating have in some cases been adopted from the former guideline without change. Information on methods, conflicts of interest, and validity of the guideline can be found in the AWMF guideline report.
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ISSN:1610-0379
1610-0387
1610-0387
DOI:10.1111/ddg.14930