DERMATOFIBROSARCOMA PROTUBERANS

Citation
Ck. Koh et al., DERMATOFIBROSARCOMA PROTUBERANS, International journal of dermatology, 34(4), 1995, pp. 256-260
Citations number
25
Categorie Soggetti
Dermatology & Venereal Diseases
ISSN journal
00119059
Volume
34
Issue
4
Year of publication
1995
Pages
256 - 260
Database
ISI
SICI code
0011-9059(1995)34:4<256:DP>2.0.ZU;2-F
Abstract
Background. Dermatofibrosarcoma protuberans (DFSP) is an uncommon mali gnant tumor of the skin, the diagnosis of which can be difficult not o nly clinically but also histologically. The tumor has a low metastatic potential, but tends to recur locally if removal is incomplete. Metho ds. We reviewed the clinical and histologic features of 19 cases of DF SP, Seen at the Department of Dermatology (14 cases) and Department of Surgery (5 cases) at the Hull Royal Infirmary between 1975 and 1992. Results. There were only 19 cases of DFSP diagnosed from a population of 500,000 over a period of 17 years. None of the cases were diagnosed clinically prior to histologic diagnosis. The highest incidence was i n the 4th decade of age. The most frequent site was on the head and ne ck. None of the lesions metastasized but there were a total of eight i ncidents of local recurrence in five patients. Histologically all the cases showed presence of storiform-pattern spindle-shaped cells and ne w collagen formation. Conclusions. Dermatofibrosarcoma protuberans is a soft tissue tumor that is often not recognized clinically due to its rarity and variable appearance. Local recurrence is frequent. A wide surgical excision is the treatment of choice.