Affiliation:
1. Department of Diagnostic Pathology and Cytology Osaka International Cancer Institute Osaka Osaka Japan
2. Department of Clinical Laboratory Osaka International Cancer Institute Osaka Osaka Japan
3. Department of Orthopedic Surgery Osaka International Cancer Institute Osaka Osaka Japan
Abstract
AbstractDermatofibrosarcoma protuberans (DFSP) is a locally aggressive superficial mesenchymal neoplasm characterized by monomorphic spindle‐cell proliferation with a storiform pattern. It can demonstrate pigmentation, myxoid changes, myoid differentiation, plaque‐like growth, and fibrosarcomatous features; its varied presentation often complicates diagnosis. We report an extremely rare case of fibrosarcomatous DFSP with features reminiscent of a pleomorphic hyalinizing angiectatic tumor (PHAT) in a 73‐year‐old male. The diagnosis was confirmed using a reverse transcription polymerase chain reaction. To the best of our knowledge, PHAT‐like changes in DFPS have not been described so far. Therefore, this report provides a novel variant of DFSP and expands the differential diagnosis of DFSP and PHAT.