Title: Eosinophilic Granulomatosis with Polyangitis – Case Report
Authors: Dr Arya Ignatious, Dr Sanju, Dr Ambily NR, Dr Suresh Raghavan
DOI: https://dx.doi.org/10.18535/jmscr/v10i10.11
Abstract
Introduction
EGPA is an uncommon small-medium vessel vasculitis. The presentation varies from asymptomatic to severe clinical manifestations including cardiovascular, gastrointestinal, renal and cns involvement.
Most common involvement is respiratory followed by dermatological manifestations
