| Literature DB >> 16008697 |
Taku Fujimura1, Ryuhei Okuyama, Tadashi Terui, Kousei Okuno, Akiko Masu, Takashi Masu, Shuko Chiba, Takahide Kunii, Hachiro Tagami, Setsuya Aiba.
Abstract
Myxofibrosarcoma or myxoid malignant fibrous histiocytoma is one of the most common fibroblastic sarcomas in older patients. It is characterized by a tendency for predominantly subcutaneous, multinodular, diffusely infiltrative growth, which may extend to the overlying dermis and present as a cutaneous lesion. Histologically, it comprises a spectrum ranging from hypocellular low-grade myxoid to high-grade pleomorphic sarcoma. Because the dermal presentation usually appears relatively banal, accurate diagnosis is sometimes challenging. In this report, we present two cases of myxofibrosarcoma with dermal involvement.Entities:
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Year: 2005 PMID: 16008697 DOI: 10.1111/j.0303-6987.2005.00368.x
Source DB: PubMed Journal: J Cutan Pathol ISSN: 0303-6987 Impact factor: 1.587