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.
作者
何婷婷
顾海萍
贾虹
HE Ting-ting;GU Hai-ping;JIA Hong(Nanjing University of Traditional Chinese Medicine, Nanjing 210023, China)
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
关键词
肢端角化症
遗传性
Acrokeratoderma
hereditary