中国麻风皮肤病杂志 ›› 2024, Vol. 40 ›› Issue (11): 809-811.doi: 10.12144/zgmfskin202411809

• 病例报告 • 上一篇    下一篇

大疱性类天疱疮继发于特应性皮炎一例

李彦波1,2*,朱军容1,3*,王上上1   

  1. 1复旦大学附属华山医院皮肤科，上海，200040；2上海市第五人民医院，上海，200240；3湖北省中医院，湖北武汉，430060 *共同第一作者
  • 出版日期:2024-11-15 发布日期:2024-10-15

Bullous pemphigoid secondary to atopic dermatitis: a case report

LI Yanbo1, 2*, ZHU Junrong1,3*, WANG Shangshang1   

  1. 1 Department of Dermatology, Huashan Hospital Affiliated to Fudan University, Shanghai 200040, China; 2 Shanghai Fifth People's Hospital, Shanghai 200240, China; 3 Hubei Provincial Hospital of TCM, Wuhan 430060, China *Co-first author
  • Online:2024-11-15 Published:2024-10-15

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摘要： 特应性皮炎和大疱性类天疱疮都是2型炎症性疾病，二者继发发生的报道国内未检索到，国外报道1例。本文报道一例有特应性皮炎病史13年的患者继发大疱性类天疱疮，给予丙种球蛋白冲击、糖皮质激素、硫唑嘌呤治疗，症状得到控制，随访6个月未复发。

关键词: 特应性皮炎, 大疱性类天疱疮

Abstract: Atopic dermatitis and bullous pemphigoid are both type 2 inflammatory diseases, the report of the combination of the two diseases was not found in China, and one case was reported abroad. We report a case of bullous pemphigoid in a patient with a 13-year history of atopic dermatitis. The symptoms were under control after treated with intravenous immunoglobulin, glucocorticoid, azathioprine, with no no recurrence after 6 months follow-up.

Key words: atopic dermatitis, bullous pemphigoid