Abstract
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic necrotizing vasculitis that affects small and medium sized vessels. EGPA is also characterized by allergic rhinitis, asthma, and prominent peripheral blood eosinophilia. EGPA is a rare disease, and its prevalence is about 11-13 cases per million. On the other hand, IgA nephropathy is the most common disease found to cause primary glomerulonephritis all over the world. There has been no case report of EGPA who had a history of IgA nephropathy.
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