以腺样体为特征的皮内痣细胞痣1例

T. Terada
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引用次数: 1

摘要

皮内瘤细胞痣是一种非常常见的皮肤错构瘤。作者在此报告两个肿瘤皮内痣细胞痣在颈部发生在一个55岁的妇女。肿瘤的组织学特征为典型的皮内瘤细胞痣,并伴有明显的腺样或腺状形成。在两个肿瘤中,在肿瘤中心可见毛囊。腺样体区细胞特征与实性区相同。实区可见模糊空泡细胞,部分区可见明显空泡细胞。肿瘤表面实心区和外侧区也表现出清晰的腺样体特征,无空泡形成。腺样体表现为含铁血黄素的轻度沉积。实性区与腺样或腺样区逐渐合并。组织化学上,包括腺样结构的肿瘤细胞有糖原,但无粘蛋白。免疫组化结果显示,两种肿瘤细胞S100蛋白、vimentin、NSE、NCAM、bcl-2呈强阳性,synaptophysin、chromogranin呈弱阳性。肿瘤细胞呈低增殖潜能;Ki-67标记指数为2%。包括腺样结构的肿瘤细胞CK AE1/3、CK CAM5.2、desmin、平滑肌肌动蛋白、HMB45、p53、p63、CD31、层粘连蛋白、4型胶原、CEA均阴性。CD34、CA125、CA19-9、CD45、GFAP、KIT、PDGFRA、CD68、雌激素受体、孕激素受体、EMA、MUC1、MUC2、MUC5AC、MUC6。这些组织学、组织化学和免疫组织化学的结果强烈提示这两个腺样结构的肿瘤属于皮内瘤细胞痣。讨论了皮内瘤细胞痣腺样结构的形成。可能的机制是细胞粘附分子的丧失。腺样体结构似乎不是退行性结构。病理学家应注意皮内瘤细胞痣可能显示腺样结构,以避免诊断混淆,例如皮肤附属物的腺瘤和腺癌。在一个病人的两个皮内瘤细胞痣中出现这种迄今未描述的情况可能暗示遗传谱系。进一步阐明皮内痣腺样结构的发生机制是今后的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intradermal nevocellular nevus with adenoid features: Report of a case
Intradermal nevocelluar nevus is a very common hamartomatous neoplasm of the skin. The author herein reports two tumors of intradermal nevocelluar nevus in the neck occurring in a 55-year-old woman. The tumors were characterized histologically by typical intradermal nevocelluar nevus with significant areas of adenoid or glandular formations. In both tumors, hair follicles were seen in centers of the tumors. The cellular features of the adenoid areas were the same as those of solid areas. In solid areas, vague vacuolated and obvious vacuolated cells were recognized in some areas. In solid areas of the surface and lateral areas of the tumors also showed clear cut adenoid features without vacuolations. The adenoid features showed mild depositions of hemosiderins. There were gradual merges between solid areas and adenoid or glandular areas. Histochemically, the tumor cells including adenoid structures had glycogen, but had no mucins. Immunohistochemically, cells of both tumors were strongly positive for S100 protein, vimentin, NSE, NCAM, and bcl-2, and were weakly positive for synaptophysin and chromogranin. The tumor cells showed low cell proliferative potential; the Ki-67 labeling index was 2%. The tumor cells including adenoid structures were negative for CK AE1/3, CK CAM5.2, desmin, smooth muscle actin, HMB45, p53, p63, CD31, laminin, type 4 collagen, CEA. CD34, CA125, CA19-9, CD45, GFAP, KIT, PDGFRA, CD68, estrogen receptor, progesterone receptor, EMA, MUC1, MUC2, MUC5AC, and MUC6. These histological, histochemical, and immunohistocheimical findings strongly suggested that the present two tumors with adenoid structures belong to intradermal nevocelluar nevus. The formation of the adenoid architectures in the intradermal nevocelluar nevus was discussed. Possible mechanisms appear loss of cell adhesions molecules. The adenoid structures seem not to be degenerative ones. Pathologists should be aware that intradermal nevocelluar nevus may show adenoid structures to avoid diagnostic confusions, for example adenoma and adenocarcinoma of skin appendages. The occurrence of this hitherto undescribed condition in two intradermal nevocelluar nevus in a patient may imply genetic lineage. To elucidate the mechanisms of adenoid structures in intradermal nevocelluar nevus seems future work.
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