Eckert F, Schaich B
Dermatologische Klinik und Poliklinik, Ludwig-Maximilians-Universität München.
Hautarzt. 1992 Feb;43(2):92-6.
This report describes a 50-year-old male patient with fibroma of tendon sheath. The tumour had grown rapidly, and clinical examination of it led to the suspicion of a giant cell tumour of tendon sheath and a vascular glomus tumour. Microscopical investigation then allowed diagnosis of the tumour as a fibroma of tendon sheath, which was characterized by spindle-shaped and stellate-shaped fibroblasts, a fibrocollagenous, partly myxoid stroma, and slit-like vessels. Immunohistochemically, most tumour cells expressed vimentin and smooth muscle actin, but not desmin. Thus, fibroma of tendon sheath can be regarded as a synovial tumour with myofibroblastic differentiation. Histologically, fibroma of tendon sheath must be differentiated from other tumours, such as giant cell tumour of tendon sheath and histiocytoma, but also from nodular fasciitis and sarcomas.
本报告描述了一名患有腱鞘纤维瘤的50岁男性患者。肿瘤生长迅速,对其进行临床检查后怀疑为腱鞘巨细胞瘤和血管球瘤。随后的显微镜检查确诊该肿瘤为腱鞘纤维瘤,其特征为梭形和星状成纤维细胞、纤维胶原性、部分黏液样基质以及裂隙样血管。免疫组织化学检查显示,大多数肿瘤细胞表达波形蛋白和平滑肌肌动蛋白,但不表达结蛋白。因此,腱鞘纤维瘤可被视为具有肌成纤维细胞分化的滑膜肿瘤。在组织学上,腱鞘纤维瘤必须与其他肿瘤相鉴别,如腱鞘巨细胞瘤和组织细胞瘤,同时也要与结节性筋膜炎和肉瘤相鉴别。