Kataoka H, Akiyama Y, Kubo S, Itoh H, Hamasuna R, Tajima N, Koono M
Second Department of Pathology, Miyazaki Medical College, Miyazaki, Japan.
Pathol Int. 1999 Sep;49(9):826-30. doi: 10.1046/j.1440-1827.1999.00946.x.
Solitary fibrous tumor (SFT) is a rare tumor that arises most commonly in the pleura. Recent evidence indicated that it is a tumor that originates from mesenchymal, probably fibroblastic, cells and is not restricted to the pleura. This report presents a case of primary SFT occurring as a dumbbell-shaped tumor of the cervical spine (C4/5) in a 46-year-old Japanese female, probably originating from the spinal rootlet. The tumor was predominantly extradural, loosely attached to the dura mater, with a small intradural extramedullary part attached to the C5 anterior and posterior rootlets. Histologically, the tumor was predominantly composed of a haphazard proliferation of spindle cells separated by abundant collagen. Immunohistochemically, the cells were strongly positive for CD34, bcl-2 and vimentin, but were negative for S-100 protein, neuron specific enolase, cytokeratin and epithelial membrane antigen. The present case and review of the literature strongly suggest that SFT is an entity that should be considered in the differential diagnosis of tumors of the cerebrospinal region.
孤立性纤维瘤(SFT)是一种罕见肿瘤,最常发生于胸膜。近期证据表明,它是一种起源于间充质细胞(可能是成纤维细胞)的肿瘤,并不局限于胸膜。本报告介绍了一例原发性SFT,发生于一名46岁日本女性的颈椎(C4/5),呈哑铃状,可能起源于脊髓小根。肿瘤主要位于硬膜外,与硬脑膜疏松相连,有一小部分硬膜内髓外部分附着于C5前后根。组织学上,肿瘤主要由被大量胶原分隔的梭形细胞杂乱增殖组成。免疫组化显示,细胞CD34、bcl-2和波形蛋白呈强阳性,但S-100蛋白、神经元特异性烯醇化酶、细胞角蛋白和上皮膜抗原呈阴性。本病例及文献复习强烈提示,SFT是一种在脑脊液区域肿瘤鉴别诊断中应予以考虑的实体。