Microscopic polyangiitis classification: Difference between revisions
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==Overview== | ==Overview== | ||
According to The International Chapel Hill Consensus Conference (CHCC) criteria based on Antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitides (AAV) | According to The International Chapel Hill Consensus Conference (CHCC) criteria based on Antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitides (AAV) into granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), including renal-limited vasculitis (RLV), and eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss). | ||
==References== | ==References== |
Revision as of 20:09, 12 April 2018
Microscopic polyangiitis Microchapters |
Differentiating Microscopic polyangiitis from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Microscopic polyangiitis classification On the Web |
American Roentgen Ray Society Images of Microscopic polyangiitis classification |
Risk calculators and risk factors for Microscopic polyangiitis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]
Overview
According to The International Chapel Hill Consensus Conference (CHCC) criteria based on Antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitides (AAV) into granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), including renal-limited vasculitis (RLV), and eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss).