Merkel cell carcinoma metastatic to the testis: report of a rare diagnosis and review of the literature

Authors

DOI:

https://doi.org/10.4322/acr.2020.198

Keywords:

Carcinoma, Merkel cell, Neoplasm Metastasis, Neuroendocrine Tumors, Testis

Abstract

Merkel cell carcinoma is an aggressive malignancy that frequently recurs/disseminates, but metastases to the genitourinary tract are rare. Only eight cases of Merkel cell carcinoma metastatic to the testis are reported. We describe the ninth case of this event and provide a review of the literature. A 58-year-old man diagnosed with Merkel cell carcinoma of the wrist, presented, 37 months later, a recurrence in the form of a testicular metastasis. The tumor consisted of a monotonous proliferation of small, blue, round cells, with immunoexpression of neuroendocrine markers and the typical dot-like paranuclear immunostaining for cytokeratin 20, in the absence of immunostaining for cytokeratin 7. The patient is alive with no evidence of disease. Clinicians should be aware of the possibility of metastatic dissemination to the testis since genital examination/imaging is not part of routine follow-up for these patients, but timely orchiectomy may be curative.

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Published

2021-01-04

How to Cite

Gigliano, D. ., Lobo, J. ., Lopes, P. ., Julião, I. ., Lobo, F. ., Azevedo, R. ., Henrique, R. ., & Rodrigues, Ângelo . (2021). Merkel cell carcinoma metastatic to the testis: report of a rare diagnosis and review of the literature. Autopsy and Case Reports, 11, e2020198. https://doi.org/10.4322/acr.2020.198

Issue

Section

Clinical Case Report and Review