Hrabko R P, Milgrom H, Schwartz R A
Arch Dermatol. 1982 Feb;118(2):106-8.
Werner's syndrome is an autosomal recessive disease characterized by juvenile cataracts, scleroderma-like skin changes, and a high incidence of neoplasms. A 57-year-old man had Werner's syndrome associated with a fibrosarcoma of the mediastinum and multiple basal cell epitheliomas. In two of these basal cell epitheliomas, since the sclerotic skin made it difficult to assess the extent of the tumor, microscopically controlled excision (Mohs' chemosurgery technique) was employed.
韦尔纳综合征是一种常染色体隐性疾病，其特征为青少年白内障、硬皮病样皮肤改变以及肿瘤高发。一名57岁男性患有韦尔纳综合征，伴有纵隔纤维肉瘤和多发性基底细胞上皮瘤。在其中两例基底细胞上皮瘤中，由于硬化的皮肤使得评估肿瘤范围变得困难，因此采用了显微镜控制下的切除（莫氏化学外科技术）。
