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奥马珠单抗治疗重度哮喘合并嗜酸性肉芽肿性多血管炎患者。病例报告。

Omalizumab treatment in patient with severe asthma and Eosinophilic Granulomatosis with Polyangiitis . A case report.

作者信息

Graziani A, Quercia O, Girelli F, Martelli A, Mirici Cappa F, Stefanini G F

机构信息

UO Medicina Interna, Ospedale degli Infermi, Faenza, Italy - AUSL Ravenna Phone: +39 054 660 12 14 E-mail:

Ambulatorio Alta Specializzazione in Allergologia, Ospedale degli Infermi, Faenza, Italia.

出版信息

Eur Ann Allergy Clin Immunol. 2014 Nov;46(6):226-8.

Abstract

Eosinophilic Granulomatosis with Polyangiitis (EGPA), formerly named Churg Strauss Syndrome, is a multisystem disorder characterized by chronic rhinosinusitis, asthma, and prominent peripheral blood eosinophilia; it is classified as a vasculitis of the small and medium sized arteries, although the vasculitis is often not clinically apparent in the initial phases of the disease. We present the case of a woman with EGPA who was frequently treated with high dose steroid therapy during hospital admission for refractory asthma. After December 2008, the date when we started Omalizumab, we observed a significative reduction of circulating eosinophils and IgE serum level, and the patient was no more hospitalized for respiratory failure or asthma attacks.

摘要

嗜酸性肉芽肿性多血管炎(EGPA),以前称为变应性肉芽肿性血管炎,是一种多系统疾病,其特征为慢性鼻窦炎、哮喘和外周血嗜酸性粒细胞显著增多;它被归类为中小动脉血管炎,尽管在疾病的初始阶段血管炎通常在临床上并不明显。我们报告一例患有EGPA的女性病例,该患者在因难治性哮喘住院期间经常接受高剂量类固醇治疗。在2008年12月我们开始使用奥马珠单抗之后,我们观察到循环嗜酸性粒细胞和血清IgE水平显著降低,并且该患者不再因呼吸衰竭或哮喘发作而住院。

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