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1 Introduction Eosinophilic Granulomatosis with Polyangiitis (EGPA), previously known as Churg-Strauss, is a rare antineutrophil cytoplasmic antibody (ANCA) associated vasculitis, with systemic multiorgan involvement [1]. EGPA is a rare condition with an incidence of 0.5–3.1 per million adults worldwide [2, 3]. It most commonly presents with late-onset asthma, chronic rhinosinusitis, often with nasal polyposis, and peripheral blood eosinophilia [4-6].
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