Fujimura Taku, Okuyama Ryuhei, Terui Tadashi, Okuno Kousei, Masu Akiko, Masu Takashi, Chiba Shuko, Kunii Takahide, Tagami Hachiro, Aiba Setsuya
Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
J Cutan Pathol. 2005 Aug;32(7):512-5. doi: 10.1111/j.0303-6987.2005.00368.x.
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.
黏液纤维肉瘤或黏液样恶性纤维组织细胞瘤是老年患者中最常见的纤维母细胞肉瘤之一。其特征是主要呈皮下、多结节、弥漫性浸润性生长,可延伸至上方真皮并表现为皮肤病变。组织学上,它包括从细胞稀少的低级别黏液样到高级别多形性肉瘤的一系列病变。由于皮肤表现通常看起来相对普通,准确诊断有时具有挑战性。在本报告中,我们呈现了两例伴有真皮受累的黏液纤维肉瘤病例。