Nistal M, Puras A, Perna C, Guarch R, Paniagua R
Department of Morphology, School of Medicine, Autonomous University of Madrid, Spain.
Histopathology. 1996 Sep;29(3):259-64. doi: 10.1111/j.1365-2559.1996.tb01400.x.
We describe an unusual fusocellular gonadal stromal tumour with a benign behaviour in the left testis from a 16-year-old man. The neoplasm consisted of a non-encapsulated proliferation of irregularly arranged, fusiform cell bundles in fibrous connective tissue. The tumour cells contained a slightly infolded nucleus, some dilated rough endoplasmic reticulum cisternae, abundant filament bundles which connected to subplasmalemmal electron-dense bodies, pinocytotic vesicles and a discontinuous basal lamina. The intercellular spaces were narrow and the tumour cells were joined by desmosomes. These cells were immunoreactive for muscle actin, alpha-actinin and vimentin. Focal immunostaining for collagen type IV was observed around the cells. No immunoreactivity for keratins, desmin S-100 protein or XIIIa factor was found. The findings suggest that the tumour arose from the peritubular myoid cells.
我们描述了一名16岁男性左侧睾丸中一种具有良性行为的罕见梭形细胞性腺间质肿瘤。肿瘤由纤维结缔组织中不规则排列的梭形细胞束的非包膜性增生组成。肿瘤细胞含有轻度内陷的细胞核、一些扩张的粗面内质网池、丰富的丝状束,这些丝状束连接到质膜下电子致密体、胞饮小泡和不连续的基膜。细胞间隙狭窄,肿瘤细胞通过桥粒连接。这些细胞对肌动蛋白、α-辅肌动蛋白和波形蛋白呈免疫反应性。在细胞周围观察到IV型胶原的局灶性免疫染色。未发现角蛋白、结蛋白、S-100蛋白或XIIIa因子的免疫反应性。这些发现提示肿瘤起源于睾丸网肌样细胞。