Merkel-sejtes daganat.

Translated title of the contribution: Merkel cell tumor

G. Fónyad, A. Rosta, E. K. Tóth, E. Szaleczky, C. Katona, Z. Sápi, L. Ungár, I. Poller

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Merkel cell cancer is a rare carcinoma arising from the neuroendocrin cells of the skin. The diagnosis is based on the clinical behaviour, histopathologic and ultrastructural findings and immunohistochemical results. An unusual case of Merkel cell carcinoma is presented. Mass from the umbiculus and a right inguinal lymph node was excised in a 63-year-old female. The histologic features of a typical, primitive small cell tumor combined with the immunohistochemical evaluations established the diagnosis. Rare polynuclear giant cells were focally present in our case. Patient was treated with combination of chemotherapy (Cisplatin, Etoposid) and radiotherapy. Control examinations showed complete respond. One year later metastasis developed. Resection of all known metastasis were performed. Two months after the laparotomy she died of metastatic disease. The autopsy did not reveal any other primary tumor. The capricious nature of the clinical course and the differences between this tumor and other carcinomas is emphasized.

Translated title of the contributionMerkel cell tumor
Original languageHungarian
Pages (from-to)1695-1697
Number of pages3
JournalOrvosi hetilap
Volume138
Issue number26
Publication statusPublished - Jun 29 1997

ASJC Scopus subject areas

  • Medicine(all)

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  • Cite this

    Fónyad, G., Rosta, A., Tóth, E. K., Szaleczky, E., Katona, C., Sápi, Z., Ungár, L., & Poller, I. (1997). Merkel-sejtes daganat. Orvosi hetilap, 138(26), 1695-1697.