Megahed M, Behrendt H, Schaffetter-Kochanek K, Plewig G
Hautklinik Heinrich-Heine-Universität Düsseldorf.
Hautarzt. 1992 Dec;43(12):781-5.
We report a 37-year-old man with neurothekeoma that developed on the tip of the nose. Histopathological examination revealed a lobulated myxoid dermal tumour. The tumour cells were spindle-shaped or bizarre configuration. In the lower part of the dermis the lesion contained abundant cells simulating glomus tumour or melanocytic naevus. Staining with S-100 protein, epithelial membrane antigen (EMA), neuron-specific enolase (NSE) and desmin were negative. The matrix of the tumour was positive for Alcian blue and periodic acid-Schiff (PAS). Electron microscopic examination showed that the lesion was composed of dendritic cells separated by abundant glassy matrix and varying amounts of collagen fibres. Some of the cells looked like fibroblasts, and others like perineurial cells. The histogenesis of the tumour is discussed with particular attention to histochemical, immunohistochemical, light and electron microscopic findings.
我们报告一名37岁男性,其鼻部尖端出现了神经鞘黏液瘤。组织病理学检查显示为分叶状黏液性真皮肿瘤。肿瘤细胞呈梭形或形态怪异。在真皮下部,病变包含大量类似血管球瘤或黑素细胞痣的细胞。S-100蛋白、上皮膜抗原(EMA)、神经元特异性烯醇化酶(NSE)和结蛋白染色均为阴性。肿瘤基质对阿尔辛蓝和过碘酸希夫(PAS)染色呈阳性。电子显微镜检查显示,病变由被大量玻璃样基质和不同数量胶原纤维分隔的树突状细胞组成。一些细胞类似成纤维细胞,另一些类似神经束膜细胞。结合组织化学、免疫组织化学、光镜和电镜检查结果对肿瘤的组织发生进行了讨论。