一例特应性皮炎加重,患者为嗜酸性粒细胞增多症伴多血管炎,用Mepolizumab治疗,并用Dupilumab联合治疗成功。

IF 0.9 Q4 RHEUMATOLOGY
Yosuke Iwadate, Yoshiyuki Arinuma, Yu Matsueda, Tomoki Tanaka, Tatuhiko Wada, Sumiaki Tanaka, Kenji Oku, Kunihiro Yamaoka
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引用次数: 0

摘要

我们报告一例60岁男性嗜酸性肉芽肿伴多血管炎(EGPA)并发特应性皮炎(AD)。患者最初接受泼尼松龙、环孢菌素A和美波珠单抗(MEPO)治疗。由于泼尼松龙减量后皮肤症状恶化,添加了dupilumab(DUP)作为皮肤活检证实的AD的辅助治疗。MEPO和DUP的联合治疗使皮肤症状迅速改善,这表明它可能是EGPA和AD患者的有效治疗选择。本病例报告强调了多学科方法在治疗EGPA和AD等复杂疾病方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of dupilumab combination therapy for exacerbation of atopic dermatitis in a patient with eosinophilic granulomatosis with polyangiitis treated with mepolizumab.

We report a 60-year-old male with eosinophilic granulomatosis with polyangiitis (EGPA) complicated with atopic dermatitis (AD). The patient was initially treated with prednisolone, cyclosporine A, and mepolizumab (MEPO). Due to worsening skin symptoms after prednisolone tapering, dupilumab (DUP) was added as an adjunctive therapy for AD confirmed by skin biopsy. The combination therapy of MEPO and DUP resulted in rapid improvement of skin symptoms, suggesting it may be an effective therapeutic option for patients with EGPA and AD. This case report emphasises the importance of a multidisciplinary approach in treating complex diseases such as EGPA and AD.

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