Coexistence of Pemphigus Foliaceus and Bullous Pemphigoid: A Case Report

被引:0
|
作者
Yuan, Jinxiang [1 ]
Yao, Xinyi [1 ]
Liu, Lvye [1 ]
Zhang, Junling [2 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Grad Sch, Tianjin, Peoples R China
[2] Tianjin Acad Tradit Chinese Med, Affiliated Hosp, Dept Dermatol, Tianjin, Peoples R China
关键词
autoimmune blistering diseases; pemphigus foliaceus; bullous pemphigoid; comorbidity; epitope spreading; direct immunofluorescence; FEATURES; DISEASE;
D O I
10.2147/CCID.S486976
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Pemphigus foliaceus (PF) and bullous pemphigoid (BP) are distinct autoimmune bullous skin diseases mediated by autoantibodies targeting adhesion molecules in desmosomes and hemidesmosomes structural proteins in the epidermal-basement membrane zone, respectively. The coexistence of PF and BP is rare. We present the case of a 72-year-old male with clinical and histological features of both PF and BP. Treatment with immunoglobulin (10 g/day for 3 days), intravenous dexamethasone sodium phosphate (5 mg/day for 10 days), oral triamcinolone (30 mg/day for 10 days), and minocycline hydrochloride (20 mg/day for 10 days) resulted in significant improvement. This rare case highlights the importance of accurate diagnosis and effective treatment strategies for the coexistence of PF and BP.
引用
收藏
页码:2725 / 2731
页数:7
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