Eosinophilic granulomatosis with polyangiitis developed during treatment with benralizmab for severe asthma: A case report and literature review.

IF 0.8 Q4 RESPIRATORY SYSTEM Respirology Case Reports Pub Date : 2024-07-09 eCollection Date: 2024-07-01 DOI:10.1002/rcr2.1431
Mitsukuni Sakabe, Kazunori Tobino, Yumi Obata, Shota Sogabe, Kazuki Uchida, Yosuke Murakami
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引用次数: 0

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare autoimmune disorder characterized by necrotizing vasculitis, asthma, and eosinophilia. We report a case of EGPA that developed during benralizumab treatment for severe asthma and provide a literature review. A 79-year-old Japanese male with severe asthma presented with generalized purpura 4 months after initiating benralizumab treatment. He had reduced his oral prednisolone dose from 7.5 to 2 mg/day. Laboratory tests revealed eosinophilia, and skin biopsy showed vasculitis with eosinophilic infiltration. He was diagnosed with EGPA and treated with corticosteroids, azathioprine, and mepolizumab, which led to rapid improvement and sustained remission. Five cases of EGPA developing during benralizumab treatment have been reported, with onset ranging from 14 to 36 weeks after initiation. Clinicians should monitor for EGPA development in patients receiving benralizumab, particularly during oral corticosteroid reduction.

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嗜酸性粒细胞肉芽肿伴多血管炎是在使用苯拉利单抗治疗严重哮喘期间出现的:病例报告和文献综述。
嗜酸性粒细胞肉芽肿伴多血管炎(EGPA)是一种罕见的自身免疫性疾病,以坏死性血管炎、哮喘和嗜酸性粒细胞增多为特征。我们报告了一例在苯拉利珠单抗治疗重症哮喘期间出现的 EGPA 病例,并提供了文献综述。一名患有重症哮喘的 79 岁日本男性在开始苯拉利珠单抗治疗 4 个月后出现全身紫癜。他将口服泼尼松龙的剂量从 7.5 毫克/天减至 2 毫克/天。实验室检查显示有嗜酸性粒细胞增多,皮肤活检显示有嗜酸性粒细胞浸润的血管炎。他被诊断为 EGPA,并接受了皮质类固醇、硫唑嘌呤和美泊利珠单抗治疗,病情迅速好转并持续缓解。据报道,在苯拉利珠单抗治疗期间出现 EGPA 的病例有 5 例,发病时间从开始治疗后的 14 周到 36 周不等。临床医生应监测接受苯拉利珠单抗治疗的患者是否出现 EGPA,尤其是在口服皮质类固醇减少期间。
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来源期刊
Respirology Case Reports
Respirology Case Reports RESPIRATORY SYSTEM-
CiteScore
1.40
自引率
0.00%
发文量
178
审稿时长
8 weeks
期刊介绍: Respirology Case Reports is an open-access online journal dedicated to the publication of original clinical case reports, case series, clinical images and clinical videos in all fields of respiratory medicine. The Journal encourages the international exchange between clinicians and researchers of experiences in diagnosing and treating uncommon diseases or diseases with unusual presentations. All manuscripts are peer-reviewed through a streamlined process that aims at providing a rapid turnaround time from submission to publication.
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