Kaye V M, Dehner L P
Department of Dermatology, University of Minnesota Medical School, Minneapolis.
Am J Dermatopathol. 1991 Feb;13(1):2-6.
Glomus tumor of the skin and subcutis is an uncommon neoplasm in which the histologic features can be mimicked by other dermal lesions of diverse types. The cell of origin is thought by most to be the pericyte, which has some of the ultrastructural features of smooth muscle. We examined six glomus tumors with a panel of antibodies including the myogenic markers, muscle-specific actin (HHF-35), and desmin; all tumors were immunoreactive for muscle-specific actin, but only two expressed desmin. Half of these tumors expressed the endothelial determinant, factor VIII-related antigen. Pseudoangiomatous melanocytic nevi stimulating glomus tumors were consistently immunoreactive for S-100 protein, which was not expressed by glomus tumors.
皮肤和皮下组织的血管球瘤是一种罕见的肿瘤,其组织学特征可被其他多种类型的皮肤病变所模仿。大多数人认为其起源细胞是周细胞,周细胞具有一些平滑肌的超微结构特征。我们用一组抗体,包括肌源性标志物肌肉特异性肌动蛋白(HHF-35)和结蛋白,检测了6例血管球瘤;所有肿瘤对肌肉特异性肌动蛋白均呈免疫反应,但只有2例表达结蛋白。这些肿瘤中有一半表达内皮决定簇,即因子VIII相关抗原。刺激血管球瘤的假血管瘤样黑素细胞痣对S-100蛋白始终呈免疫反应,而血管球瘤不表达S-100蛋白。