Eosinophilic Granulomatosis With Polyangiitis: Dissecting the Pathophysiology
Abstract
Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare multisystemic disease classified both amongst hypereosinophilic disorders and ANCA-associated vasculitis. Vessel inflammation and eosinophilic proliferation are the hallmarks of the disease and main effectors of organ damage. Two distinct disease phenotypes have classically been described according to ANCA-status: the ANCA-negative subset with eosinophil-driven manifestation and the...
Paper Details
Title
Eosinophilic Granulomatosis With Polyangiitis: Dissecting the Pathophysiology
Published Date
Feb 24, 2021
Journal
Volume
8
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