MERKEL-CELL-CARCINOMA - FOLLOW-UP REPORT ON 10 PATIENTS CURRENT DIAGNOSIS AND THERAPY

Citation
A. Hauschild et al., MERKEL-CELL-CARCINOMA - FOLLOW-UP REPORT ON 10 PATIENTS CURRENT DIAGNOSIS AND THERAPY, Langenbecks Archiv fur Chirurgie, 382(4), 1997, pp. 185-191
Citations number
25
Categorie Soggetti
Surgery
ISSN journal
00238236
Volume
382
Issue
4
Year of publication
1997
Pages
185 - 191
Database
ISI
SICI code
0023-8236(1997)382:4<185:M-FRO1>2.0.ZU;2-V
Abstract
Merkel cell carcinoma (MCC) is a rare neoplasm of the skin predominant ly found on the head and extremities. Clinically MCC presents as a rap idly growing red or violaceous, dome-shaped, solitary tumor. The clini cal and histological diagnosis of MCC remains difficult. Distinction f rom poorly differentiated small cell primary tumors or metastasis requ ires immunohistochemical analysis and - if available - electron-micros copic studies. We report on the follow-up of 10 patients with MCC trea ted in the past 6 years at our department. In nine patients the tumors were completely removable; in one patient with a large primary tumor of the upper lip no histologically proven complete excision could be p erformed. After a median follow-up of 42 months, local recurrence or l ymph node involvement was observed in three patients. Two patients die d following disseminated metastases, one elderly patient due to cardia c insufficiency. Our observations demonstrate that MCC is a potentiall y aggressive cutaneous tumor. Adequate primary surgical and adjuvant t herapy as well as careful follow-up are mandatory.