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Published on: June 23, 2014
Hydralazine-induced autoimmune disease: comparison to idiopathic lupus and ANCA-positive vasculitis
Naoto Yokogawa1, Frederick B Vivino
1Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, USA. yokogawan@aol.com
Abstract:
We report two cases of hydralazine-induced vasculitis with rare complications: pulmonary renal syndrome and digital gangrene. We also review 68 published cases of hydralazine-induced vasculitis. Hydralazine-induced vasculitis mimics idiopathic antineutrophil cytoplasmic antibody (ANCA)-positive vasculitis. However, it also produces other autoantibodies, such as antinuclear antibodies, antihistone antibodies, anti-dsDNA antibodies, and antiphospholipid antibodies. Patients with hydralazine-induced vasculitis typically have a more severe course than those with hydralazine-induced lupus, predominantly due to renal vasculitis, and require a more aggressive treatment.
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