Inoue Y, Yamaizumi M, Ono T
Department of Dermatology, Kumamoto University School of Medicine, Japan.
J Dermatol. 1995 May;22(5):360-4. doi: 10.1111/j.1346-8138.1995.tb03405.x.
A 12-year-old boy was diagnosed as having group D xeroderma pigmentosum based on the results of unscheduled DNA synthesis (UDS) tests and complementation tests. More than 200 moles were distributed all over his body, including the unexposed areas of his torso and scalp. All of eight removed specimens were compatible histologically with nevocellular nevi.
一名12岁男孩根据非预定DNA合成(UDS)试验和互补试验结果被诊断为患有D组着色性干皮病。他全身分布着200多个痣,包括躯干和头皮的未暴露部位。切除的8个标本在组织学上均与痣细胞痣相符。