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Case report reveals rapidly progressive glomerulonephritis in an elderly female, suggesting possible links to IgA vasculitis.
Immunoglobulin A nephropathy (IgAN) is a common cause of glomerulonephritis that can progress to end-stage renal disease (ESRD). IgA vasculitis, a systemic small vessel vasculitis, is a recognized secondary cause of IgAN. Although rare, rapidly progressive glomerulonephritis (RPGN) can occur in the context of IgA vasculitis, with drug-induced immune responses implicated in some cases.
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Maramba et al. (2026) studied this question.
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