中国麻风皮肤病杂志 ›› 2022, Vol. 38 ›› Issue (12): 881-883.doi: 10.12144/zgmfskin202212881

• 病例报告 • 上一篇    下一篇

嗜酸性肉芽肿性多血管炎一例

朱小美1,陈思远2,黄长征2,刘冬先1,夏颖1   

  1. 1华中科技大学同济医学院附属同济医院皮肤科，武汉，430030；2华中科技大学同济医学院附属协和医院皮肤科，武汉，430022
  • 出版日期:2022-12-15 发布日期:2022-10-26

Eosinophilic granulomatous polyangiitis: a case report

ZHU Xiaomei1, CHEN Siyuan2, HUANG Changzheng2, LIU Dongxian1, XIA Ying1   

  1. 1 Department of Dermatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China; 2 Department of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
  • Online:2022-12-15 Published:2022-10-26

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摘要： 患者，女，29岁。头面、手足散在血疱样丘疹、结节3天。皮肤科检查：面部、手足散在绿豆至花生大丘疹、结节，质地稍硬，浸润明显，表面可见紫癜样改变，部分皮损破溃结痂。结合临床症状、实验室及组织病理检查，诊断为嗜酸性肉芽肿性多血管炎。

关键词: 嗜酸性肉芽肿性多血管炎, 紫癜, 丘疹

Abstract: A 29-year-old female presented with scattered blood blister papules and nodules on her head, face, hands and feet for 3 days. Based on the laboratory examination, clinical and histological features, diagnosis of eosinophilic granulomatous polyangiitis (EGPA) was made.

Key words: eosinophilic granulomatous polyangiitis (EGPA), purpura, papule