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

Authors :
Graziani A
Quercia O
Girelli F
Martelli A
Mirici Cappa F
Stefanini GF
Source :
European annals of allergy and clinical immunology [Eur Ann Allergy Clin Immunol] 2014 Nov; Vol. 46 (6), pp. 226-8.
Publication Year :
2014

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.

Details

Language :
English
ISSN :
1764-1489
Volume :
46
Issue :
6
Database :
MEDLINE
Journal :
European annals of allergy and clinical immunology
Publication Type :
Academic Journal
Accession number :
25398166