Department of Paediatrics, Riga Stradiņš University, Riga, Latvia.
Clinic of Pediatric Diseases, Children's Clinical University Hospital, Riga, Latvia.
Pediatr Pulmonol. 2023 Mar;58(3):973-979. doi: 10.1002/ppul.26249. Epub 2022 Dec 5.
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.
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。