Original paper
Simultaneous development of IgA vasculitis and eosinophilic granulomatosis with polyangiitis
Abstract
Immunoglobulin A (IgA) vasculitis (IgAV) is a small vessel vasculitis presenting cutaneous purpura, arthralgias and/or arthritis, acute enteritis and glomerulonephritis caused by deposition of the IgA1-mediated immune complex. Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) characterised by eosinophil-rich and granulomatous inflammation in small to medium-sized...
Paper Details
Title
Simultaneous development of IgA vasculitis and eosinophilic granulomatosis with polyangiitis
Published Date
Oct 23, 2019
Volume
4
Issue
1
Pages
63 - 69
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Notes
History