| Literature DB >> 24471461 |
Kensaku Yamaga1, Kohei Shomori, Hideki Yamashita, Koji Endo, Chikako Takeda, Takeshi Minamizaki, Haruhiko Yoshida, Ryota Teshima, Hisao Ito.
Abstract
Proliferative fasciitis (PF) is a benign, discrete proliferation of fibroblasts or myofibroblasts in soft tissue. Proliferative fasciitis mostly occurs in adults and is often confused with a sarcoma because of its rapid growth and peculiar histological features. We report a case of PF mimicking a sarcoma which developed in a 13-year-old boy, who noticed a painful tumor, with gradual enlargement, in his right lower leg. Magnetic resonance imaging revealed that the tumor measured 34 mm × 20 mm × 41 mm and was located in the subcutaneous tissue. The tumor was surgically resected. Pathologically, the tumor was composed of a proliferation of atypical spindle cells, admixed with larger ganglion-like cells. Immunohistochemically, the tumor cells were positive for vimentin, cytokeratin, smooth muscle actin, HHF-35 and Fli-1. The tumor was subsequently diagnosed as a PF, although it was difficult to differentiate from a sarcoma. Five years after surgery, the postoperative course has been uneventful with no recurrence or metastasis.Entities:
Keywords: child; cytokeratin; lower leg; proliferative fasciitis; soft tissue tumor
Mesh:
Year: 2014 PMID: 24471461 DOI: 10.1111/1346-8138.12384
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005