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This study aimed to compare patient self-reported and physician-reported clinical manifestations, treatments, and outcomes in patients with eosinophilic granulomatosis with polyangiitis (EGPA), one of the antineutrophil cytoplasmic antibody (ANCA)–associated vasculitides. EGPA is a complex multisystem disorder that can involve any combination of many manifestations, especially including asthma, rhinosinusitis, eosinophilia, and vasculitis in various organs.
Interact J Med Res 2022;11(1):e27273
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