中国麻风皮肤病杂志 ›› 2021, Vol. 37 ›› Issue (1): 37-39.doi: 10.12144/zgmfskin202101037

• 病例报告 • 上一篇    下一篇

炎症性浅表播散性汗孔角化症一例

杨曦,宋海燕,王彦,王丽华   

  1. 山东第一医科大学附属济南市中心医院皮肤科，济南，250013
  • 出版日期:2021-01-15 发布日期:2021-01-05
  • 通讯作者: 王丽华，E-mail: 15318816237@163.com

Inflammatory disseminated superficial porokeratosis: a case report

YANG Xi, SONG Haiyan, WANG Yan, WANG Lihua   

  1. Department of Dermatology, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, China
  • Online:2021-01-15 Published:2021-01-05
  • Contact: WANG Lihua, E-mail: 15318816237@163.com

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摘要： 患者，男，64岁。全身褐色环形斑块2年，伴瘙痒2个月。组织病理示：表皮角化不全，角化过度，可见角化不全柱，其下方棘层散在角化不良细胞，基底层灶状液化变性，真皮见团块状淋巴细胞为主的炎细胞浸润。诊断：炎症性浅表播散性汗孔角化症。给予阿维A 30 mg/d口服治疗，皮损部分消退，目前随访中。

关键词: 炎症性浅表播散性汗孔角化症, 发疹性瘙痒性丘疹型汗孔角化症

Abstract: A 64-year-old male presented with brown annular plaques on his body for 2 years, with itching for 2 months. Physical examination showed parakeratosis, hyperkeratosis, cornoid lamella, dyskeratosis cells below the cornoid lamella, and lymphocytes infiltrate in the dermis. The diagnosis of inflammatory disseminated superficial porokeratosis was made. The patient was treated with oral acitretin 30mg per day. The skin lesions improved and partly subsided. The patient is currently under follow-up.

Key words: inflammatory disseminated superficial porokeratosis, eruptive pruritic papule porokeratosis