Nephritic Syndrome
Perola Lamba1, Ki Heon Nam2, Jigar Contractor3
1Department of Medicine, Division of General Internal Medicine, Section of Hospital Medicine, Weill Cornell Medical College, 525 East 68th Street, Box 331, New York, NY 10065, USA.
Abstract:
Nephritic syndrome is a constellation of hematuria, proteinuria, hypertension, and in some cases acute kidney injury and fluid retention characteristic of acute glomerulonephritis. Infection-related glomerulonephritis, IgA nephropathy, lupus nephritis, membranoproliferative glomerulonephritis, and antineutrophil cytoplasmic antibody-associated vasculitis are the most common diseases in nephritic syndrome that primary care physicians might encounter in practice such that a solid comprehension of these can lead to earlier detection. This article describes the pathophysiology, incidence, clinical presentation, treatment, and disease progression of these nephritic syndrome entities, and provides guidance for when to refer to a nephrologist.
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