Fukunaga M, Ushigome S, Nomura K, Ishikawa E
Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.
Pathol Int. 1995 Dec;45(12):952-7. doi: 10.1111/j.1440-1827.1995.tb03421.x.
Solitary fibrous tumors (SFT) are rare spindle cell neoplasms generally associated with the serosal surface, especially the pleura. Two SFT are reported arising in the nasal cavity and orbit, occurring in a 33 year old female and a 21 year old male, respectively. The lesions lacked the characteristic features of other recognized neoplasms that occur in these regions. Immunohistochemically, the tumors cells were diffusely and strongly positive for vimentin and CD34 and some or many tumor cells expressed neuron-specific enolase and Leu-7. Ultrastructurally, the tumor cells showed no distinct features although they were suggested to be primitive mesenchymal or fibroblast-like cells. Both tumors were diploid by flow cytometry. The two patients have had benign clinical courses with limited follow-up. Our findings suggest that SFT is of mesenchymal cell origin and support another location for SFT, indicating additional evidence against mesothelial origin. SFT should be included in the differential diagnosis of spindle cell tumors arising in the nasal cavity and orbit.
孤立性纤维性肿瘤(SFT)是一种罕见的梭形细胞肿瘤,通常与浆膜表面相关,尤其是胸膜。据报道,有两例SFT分别发生在鼻腔和眼眶,患者分别为一名33岁女性和一名21岁男性。这些病变缺乏这些区域其他公认肿瘤的特征性表现。免疫组织化学检查显示,肿瘤细胞波形蛋白和CD34弥漫性强阳性,部分或许多肿瘤细胞表达神经元特异性烯醇化酶和Leu-7。超微结构上,肿瘤细胞虽提示为原始间充质细胞或成纤维细胞样细胞,但无明显特征。流式细胞术检测显示两个肿瘤均为二倍体。两名患者临床过程均为良性,随访时间有限。我们的研究结果提示SFT起源于间充质细胞,并支持SFT的另一个发病部位,这为反对其间皮起源提供了更多证据。SFT应纳入鼻腔和眼眶梭形细胞肿瘤的鉴别诊断。