
Eosinophilic Granulomatous Polyangiitis with Autoimmune Hemolytic Anemia: A Case Report and Review of the Literature
Introduction Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare, multisystem disorder encompassing eosinophilia and Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis. Histopathologically, EGPA is characterized by profound …