遗传性半透明性丘疹性肢端角化症二例  

Hereditary papulotranslucent acrokeratoderma: two cases report

作　　者：何婷婷[1] 顾海萍[1] 贾虹 HE Ting-ting;GU Hai-ping;JIA Hong(Nanjing University of Traditional Chinese Medicine, Nanjing 210023, China)

机构地区：[1]南京中医药大学,南京210023 [2]中国医学科学院皮肤病医院

出　　处：《实用皮肤病学杂志》2018年第3期181-182,185,共3页Journal of Practical Dermatology

摘　　要：遗传性半透明性丘疹性肢端角化症是一种罕见的发生于掌跖部位,表现为黄白色半透明丘疹的皮肤病,本病多有家族史,但亦存在散发病例。本文报道2例散发性病例,患者均为中青年女性,青少年时期发病,双手累及,临床症状典型,治疗效果均不甚理想。Hereditary papulotranslucent acrokeratoderma is a rare disease, usually with a family history, characterized by yellowish white and translucent papules on palms and soles. The disease usually has a family history, but there are still some sporadic cases. Two sporadic cases were reported, both were young and middle-aged women. The disease developed in adolescence and involved hands, and the clinical symptoms of which were typical, but the effectiveness of the treatment was not satisfactory.

关 键 词：肢端角化症 遗传性 

分 类 号：R758.53[医药卫生—皮肤病学与性病学]