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
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.