摘要
患者女,68岁。全身散在褐色角化性丘疹伴瘙痒2年余。皮损组织病理检查示角化过度,表皮增生,柱状角化不全,部分角化不全柱下可见部分角化不良细胞,真皮浅层片状淋巴细胞浸润。全基因组外显子测序提示患者MVK基因突变。诊断:播散性浅表性光线性汗孔角化症,治疗:口服异维A酸软胶囊、抗组胺药和外用维A酸药物3个月余,皮疹逐渐消退,瘙痒缓解,目前患者仍在随访中。
A 68-year-old woman had discrete brown keratinized papule with pruritus all over the body for more than 2 years. Histopathologic examination showed hyperkeratosis, epidermal hyperplasia, incomplete columnar keratinization, some keratinized cells with partial keratinization, and lamellar lymphocyte infiltration in superficial dermis. Genome-wide exome sequencing suggested MVK gene mutations. It was diagnosed as disseminated superficial actinic porokeratosis. After treatment of oral isotretinoin, antihistamine and external retinoic acid for more than 3 months, the skin lesions gradually subsided and the pruritus was under control. The patient is now being followed up.
作者
邓婕
梁晓冬
叶瑞贤
刘焕颜
熊绮颖
田歆
张锡宝
DENG Jie;LIANG Xiao-dong;YE Rui-xian;LIU Huan-yan;XIONG Qi-ying;TIAN Xin;ZHANG Xi-bao(Department of Dermatology,the Afilited Haspital of Southern Medical Universily,Foshan 528244,China)
出处
《临床皮肤科杂志》
CAS
CSCD
北大核心
2020年第5期283-285,共3页
Journal of Clinical Dermatology
基金
广东省自然科学基金(2016A030313471)资助项目。