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一例美泊利珠单抗治疗嗜酸性肉芽肿性多血管炎患者中重度特应性皮炎恶化后接受度普利尤单抗联合治疗的病例。

A case of dupilumab combination therapy for exacerbation of atopic dermatitis in a patient with eosinophilic granulomatosis with polyangiitis treated with mepolizumab.

机构信息

Department of Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Kanagawa, Japan.

出版信息

Mod Rheumatol Case Rep. 2023 Dec 29;8(1):159-162. doi: 10.1093/mrcr/rxad059.

DOI:10.1093/mrcr/rxad059
PMID:37804249
Abstract

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.

摘要

我们报告了一例 60 岁男性,患有嗜酸性肉芽肿伴多血管炎(EGPA)合并特应性皮炎(AD)。该患者最初接受泼尼松龙、环孢素 A 和美泊利珠单抗(MEPO)治疗。由于泼尼松龙减量后皮肤症状恶化,皮肤活检证实 AD 后加用度普利尤单抗(DUP)作为辅助治疗。MEPO 和 DUP 的联合治疗导致皮肤症状迅速改善,表明其可能是 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 等复杂疾病中的重要性。

相似文献

1
A case of dupilumab combination therapy for exacerbation of atopic dermatitis in a patient with eosinophilic granulomatosis with polyangiitis treated with mepolizumab.一例美泊利珠单抗治疗嗜酸性肉芽肿性多血管炎患者中重度特应性皮炎恶化后接受度普利尤单抗联合治疗的病例。
Mod Rheumatol Case Rep. 2023 Dec 29;8(1):159-162. doi: 10.1093/mrcr/rxad059.
2
Eosinophilic granulomatosis polyangiitis (EGPA) complicated with periaortitis, precipitating role of dupilumab? A case report a review of the literature.嗜酸性肉芽肿性多血管炎(EGPA)并发大动脉炎,度普利尤单抗的诱发作用?病例报告及文献复习。
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Development of eosinophilic granulomatosis with polyangiitis during the clinical course of microscopic polyangiitis: A case report.显微镜下多血管炎临床病程中嗜酸性肉芽肿伴多血管炎的发展:一例报告。
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Polyangiitis overlap syndrome of granulomatosis with polyangiitis (Wegener's granulomatosis) and eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome).肉芽肿性多血管炎(韦格纳肉芽肿)与嗜酸性肉芽肿性多血管炎(变应性肉芽肿性血管炎)重叠综合征。
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引用本文的文献

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Dupilumab-induced Eosinophilic Granulomatosis with Polyangiitis Complicated by Peripheral Neuropathic Pain: a Case Report and Literature Review.度普利尤单抗诱发的嗜酸性肉芽肿性多血管炎并发周围神经性疼痛:一例报告及文献综述
J Clin Immunol. 2025 Jul 24;45(1):114. doi: 10.1007/s10875-025-01914-x.
2
Dupilumab Use in Patients With Hypereosinophilic Syndromes: A Multicenter Case Series and Review of the Literature.度普利尤单抗在高嗜酸性粒细胞综合征患者中的应用:一项多中心病例系列研究及文献综述
J Allergy Clin Immunol Pract. 2025 Jan;13(1):167-175.e6. doi: 10.1016/j.jaip.2024.10.036. Epub 2024 Nov 6.
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Successful combination therapy of mepolizumab and dupilumab in a patient with EGPA: a future therapeutic option?
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Insight into IL-5 as a Potential Target for the Treatment of Allergic Diseases.深入了解白细胞介素-5作为治疗过敏性疾病的潜在靶点。
Biomedicines. 2024 Jul 10;12(7):1531. doi: 10.3390/biomedicines12071531.