| Literature DB >> 16287497 |
Tomomi Kusumi1, Shinji Nishikawa, Masanori Tanaka, Taro Ogawa, Hiromichi Jin, Fuyuki Sato, Satoshi Toh, Tadashi Hasegawa, Hiroshi Kijima.
Abstract
Low-grade fibromyxoid sarcoma (LGFMS) is a rare tumor. Reported herein is a case of LGFMS arising in the big toe. The patient was a 58-year-old man who underwent excision of the tumor. The tumor was well-demarcated. Histologically, there were proliferating spindle-shaped tumor cells arranged in a whorled growth pattern, and the stroma showed hyalinized collagen bundles and a myxoid matrix. Nuclear mitotic figures were conspicuous in part. A large rosette-like structure with hyalinized stroma was found, which is characteristic of LGFMS. The differential diagnosis included tumor occurrence in adults; tending to arise in distal extremities; and having bland fibromyxoid histological features, such as fibroma of tendon sheath, low-grade myxofibrosarcoma and acral myxoinflammatory fibroblastic sarcoma. It was not possible to detect the FUS/CREB3L2 and FUS/CREB3L1 fusion genes from the formalin-fixed and paraffin-embedded tissue, although the histological features of the present case were typical of LGFMS. LGFMS may become more common with time, and unique cases may accumulate.Entities:
Mesh:
Year: 2005 PMID: 16287497 DOI: 10.1111/j.1440-1827.2005.01910.x
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534