Morphological patterns of metastases from combined Merkel cell carcinomas: study of an eastern Canadian cohort of cases

Jennette R. Gruchy, Sylvia Pasternak, Thai Yen Ly, Ryan C. DeCoste, Kirsten E. Fleming, Phillip M. Moss, Michael D. Carter, Noreen M. Walsh

Résultat de recherche: Articleexamen par les pairs

3 Citations (Scopus)

Résumé

Combined Merkel cell carcinomas are hybrid tumors composed of neuroendocrine and other phenotypic (usually squamous) elements. They form a minority of Merkel cell carcinomas (MCCs) as a whole, are usually Merkel cell polyomavirus-negative, and have rarely been segregated for specific study. Sporadic reports have indicated that metastases from these tumors can show a combined phenotype. We retrospectively studied 38 cases (24 men [63%], 14 women [37%], mean age 78 years [range, 46–99 years]) of combined MCC. Metastases occurred in 20 patients (53%) (at presentation and/or in follow-up [mean 38 months (range, 0.6–185 months)]). Those from 17 individuals (45%) were examined microscopically. These were mainly nodal in distribution. In 12 patients (71%), the secondary deposits were of pure neuroendocrine type, whereas in 5 (29%), combined deposits were identified. Squamous elements were the most common divergent component, in the primary and secondary tumors. The combined metastases varied from obvious squamous nests in a neuroendocrine background to scattered bizarre tumor giant cells expressing CK5/6 on immunohistochemistry. In one case, individual nodes within a single basin displayed purely squamous or purely neuroendocrine deposits. The mean overall survival in the cohort was 48 months (range, 30–67 months) and the mortality was 82%. Our work sheds light on the frequency and patterns of metastases in combined MCCs. In concert with the poor outcome data documented by others, it also raises a question as to the potential prognostic significance of a combined phenotype per se, independent of a virus-negative status and other variables. This issue deserves further study.

Langue d'origineEnglish
Pages (de-à)47-55
Nombre de pages9
JournalHuman Pathology
Volume129
DOI
Statut de publicationPublished - nov. 2022

Note bibliographique

Publisher Copyright:
© 2022 Elsevier Inc.

ASJC Scopus Subject Areas

  • Pathology and Forensic Medicine

PubMed: MeSH publication types

  • Journal Article

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