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美泊利珠单抗:治疗嗜酸性肉芽肿伴多血管炎患儿的策略。

Mepolizumab: Therapeutic strategy for a pediatric patient with eosinophilic granulomatosis with polyangiitis.

机构信息

Department of Paediatrics, Riga Stradiņš University, Riga, Latvia.

Clinic of Pediatric Diseases, Children's Clinical University Hospital, Riga, Latvia.

出版信息

Pediatr Pulmonol. 2023 Mar;58(3):973-979. doi: 10.1002/ppul.26249. Epub 2022 Dec 5.

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA; formerly known as Churg-Strauss syndrome) is classified as an antineutrophil cytoplasmic antibody (ANCA)-associated small vessel vasculitis. It is a multisystem disorder and can affect every organ system. EGPA is a rare disease, with an estimated prevalence of 1/70,000-100,000 in Europe. As its onset usually occurs in adulthood, data from pediatric patients are limited. We present here a very rare practical EGPA clinical case involving a pediatric patient. Presently, data on mepolizumab usage in pediatric patients are limited, with only a few case reports published.

摘要

嗜酸性肉芽肿性多血管炎(EGPA;以前称为 Churg-Strauss 综合征)被归类为抗中性粒细胞胞质抗体(ANCA)相关性小血管血管炎。它是一种多系统疾病,可影响每个器官系统。EGPA 是一种罕见疾病,在欧洲的患病率估计为每 70,000-100,000 人中有 1 例。由于其发病通常发生在成年期,因此儿科患者的数据有限。我们在此介绍了一个非常罕见的儿科患者 EGPA 实际临床病例。目前,关于美泊利珠单抗在儿科患者中的使用的数据有限,仅发表了少数病例报告。

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