The Prevalence and Management of Pauci-Immune Glomerulonephritis and Vasculitis in Western Countries
Author(s) -
Sophia Lionaki,
John Boletis
Publication year - 2015
Publication title -
kidney diseases
Language(s) - English
Resource type - Journals
eISSN - 2296-9381
pISSN - 2296-9357
DOI - 10.1159/000442062
Subject(s) - vasculitis , glomerulonephritis , medicine , rapidly progressive glomerulonephritis , immunology , dermatology , pathology , disease , kidney
Pauci-immune glomerulonephritis is the most common cause of aggressive glomerulonephritis and occurs as a renal-limited disease or as a component of systemic necrotizing small-vessel vasculitis. It is characterized by paucity of staining for immunoglobulins, by immunofluorescence along with fibrinoid necrosis and crescent formation by light microscopy, while the vast majority of patients have anti-neutrophil cytoplasmic antibodies (ANCA) in their circulation, which also participate in the pathogenesis of the disease.
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