进行性特发性皮肤萎缩合并硬化性苔藓1例  

Progressive Idiopathic Atrophoderma with Lichen Sclerosus:A Case Report

作　　者：皮佩瑶 朱小美 PI Peiyao;ZHU Xiaomei(Department of Dermatology,Xian Fifth Hospital,Shaanxi TCM and WM Integrative Hospital,Xi'an 710082,China;Department of Dermatology,Tongji Hospital,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China)

机构地区：[1]陕西省中西医结合医院(西安市第五医院)皮肤科,陕西西安710082 [2]华中科技大学同济医学院附属同济医院皮肤科,湖北武汉430030

出　　处：《中国皮肤性病学杂志》2023年第2期223-227,共5页The Chinese Journal of Dermatovenereology

摘　　要：患者男,26岁,左侧腰腿部片状斑疹16年,加重4年。皮肤科情况:左侧腹部、左侧腰部、左下肢伸侧可见暗棕色萎缩斑,表面光滑,边界较清,其下方静脉纹理显露;左下肢皮损中央可见不规则形瓷白色硬化性斑片。经皮肤检查、反射式共聚焦显微镜及皮肤病理检查诊断为进行性特发性皮肤萎缩合并硬化性苔藓。A 26-year-old male presented with patchy macule on the left waist and leg for 16 years and aggravated for 4 years. Dark brown atrophic patches were observed on the left abdomen, left waist and extensional side of the left lower limb, with smooth surface and clear boundary, and the veins underneath were seen. There was an irregularly shaped porcelain white sclerosing plaque in the center of the skin lesion of the left lower limb. Progressive idiopathic atrophoderma with lichen sclerosus were diagnosed by dermatoscopy, reflection confocal microscopy and skin histopathological examination.

关 键 词：进行性特发性皮肤萎缩 硬化性苔藓 

分 类 号：R758.56[医药卫生—皮肤病学与性病学]