Mehta V R, Potdar R
Int J Dermatol. 1985 Sep;24(7):444-6.
A dominant inheritance leading to development of nevoid basal cell epitheliomas on the face and follicular atrophoderma on the extremities constitute the two constant manifestations of Bazex syndrome. A patient with both manifestations on the trunk who fulfilled all the criteria for a diagnosis of nevoid basal cell epitheliomas is described. Histopathology of the basal cell cancer corresponded to that of the fibroepithelial tumor, thus differing from the more common nodular and trichoepitheliomatous presentations. Difficulty in associating the atrophoderma with a hair follicle (histologically) arises because the latter ceases to exist as a functional unit.
导致面部痣样基底细胞上皮瘤和四肢毛囊性皮肤萎缩的显性遗传构成了巴泽克斯综合征的两种常见表现。本文描述了一名躯干同时出现这两种表现且符合痣样基底细胞上皮瘤所有诊断标准的患者。基底细胞癌的组织病理学与纤维上皮瘤相符,因此不同于更常见的结节性和毛发上皮瘤表现。由于毛囊作为一个功能单位已不复存在,所以(在组织学上)难以将皮肤萎缩与毛囊联系起来。