Dermatofibrosarcoma protuberans is a low-grade sarcoma of the skin wit
h well characterized clinical and histopathological features. The lesi
on frequently appears as a plaque on the trunk or on the extremities o
f middle-aged adults. Microscopically, the tumor is composed of monomo
rphous spindle cells arranged in storiform pattern and embedded in a s
parse to moderately dense fibrous stroma. We report on two unusual cas
es of dermatofibro-sarcoma protuberans in which neoplastic cells were
diffusely replaced by sclerotic tissue in more than 50% of the entire
tumor in both cases, no external trauma or radiotherapy were recorded.
Since tumor regression has been defined as a loss of tumor mass in th
e absence of any treatment (or trauma) we believe that sclerosis in DF
SP may represent a manifestation of regression and not, as previously
suggested, a new variant of the neoplasm.