Evidence map›Paper›PMID 42830549›Full record

ArticleThe American journal of case reports2026

When Infection Mimics Vasculitis: Hydralazine-Induced ANCA-Associated Crescentic Glomerulonephritis in the Setting of Active Infective Endocarditis.

Mohmmed Saleh, Shahrzad Zavoshi, Paul Fozo

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Article in The American journal of case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mohmmed SalehDepartment of Internal Medicine, Henry Ford St. John Hospital, Detroit, MI, USA.
Shahrzad ZavoshiDepartment of Internal Medicine, Henry Ford St. John Hospital, Detroit, MI, USA.
Paul FozoDepartment of Internal Medicine, Henry Ford St. John Hospital, Detroit, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Hydralazine-induced antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a rare cause of pauci-immune crescentic glomerulonephritis that can closely mimic infection-related renal disease, particularly in the setting of active infective endocarditis. Distinguishing between infection-related glomerulonephritis and drug-induced ANCA-associated vasculitis is clinically important because management strategies differ substantially. We present a case supporting the hypothesis that persistent renal dysfunction despite microbiologic control of infective endocarditis, together with pauci-immune biopsy findings and chronic hydralazine exposure, should prompt consideration of hydralazine-induced ANCA-associated vasculitis rather than infection-related glomerulonephritis. CASE REPORT We report the case of a 58-year-old man with a history of bicuspid aortic valve who presented with fatigue, anemia, and acute kidney injury. Blood cultures grew Streptococcus mutans, and echocardiography demonstrated aortic valve vegetations consistent with subacute infective endocarditis. Laboratory evaluation revealed hypocomplementemia, proteinuria, hematuria, and elevated MPO and PR3 ANCA titers. Despite appropriate antimicrobial therapy and clearance of bacteremia, renal dysfunction persisted. Renal biopsy demonstrated pauci-immune crescentic glomerulonephritis consistent with ANCA-associated vasculitis. Further review of the patient's medications revealed long-term hydralazine therapy, raising concern for hydralazine-induced ANCA-associated vasculitis. Hydralazine was discontinued, and the patient was initiated on high-dose corticosteroid therapy with plans for additional immunosuppressive therapy following recovery from cardiac surgery. The patient subsequently underwent successful bioprosthetic aortic valve replacement with gradual stabilization of renal function. CONCLUSIONS This case highlights the diagnostic overlap between infective endocarditis-associated glomerulonephritis and hydralazine-induced ANCA-associated vasculitis. In patients with infective endocarditis who develop persistent renal dysfunction despite appropriate antimicrobial therapy, particularly in the setting of ANCA positivity and chronic hydralazine use, renal biopsy and medication review are essential to establish the correct diagnosis and guide appropriate management.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisEndocarditisEndocarditis, BacterialGlomerulonephritisHydralazineAntibodies, Antineutrophil CytoplasmicDiagnosis, DifferentialHumansMaleMiddle AgedAntibodies, Antineutrophil CytoplasmicHydralazine

Identifiers

PMID42830549
PMCPMC13653482

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