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Lupus
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case-report

Hypocomplementemic urticarial vasculitis with Jaccoud's arthropathy and valvular heart disease: case report and review of the literature

H Amano

Department of Rheumatology and Internal Medicine, Juntendo University, Tokyo, Japan amano{at}med.juntendo.ac.jp

N Furuhata

Department of Rheumatology and Internal Medicine, Juntendo University, Tokyo, Japan

N Tamura

Department of Rheumatology and Internal Medicine, Juntendo University, Tokyo, Japan

Y Tokano

Department of Rheumatology and Internal Medicine, Juntendo University, Tokyo, Japan

Y Takasaki

Department of Rheumatology and Internal Medicine, Juntendo University, Tokyo, Japan

We describe a female Japanese patient with concomitant hypocomplementemic urticarial vasculitis, Jaccoud's arthropathy and valvular heart disease. In 1996, she developed arthritis with swelling of both proximal interphalangeal joints and urticarial vasculitis on both arms that was resolved by administration of glucocorticoid (prednisolone 30 mg/day). Tests for antineutrophil cytoplasmic antibodies, antinuclear antibody and rheumatoid factor gave negative results. The findings of a skin biopsy examination were consistent with ‘leukocytoclastic vasculitis'. During 10 years of observation, the patient manifested polyarthritis leading to progressive deformity of the joints of the hands and feet (without loss of cartilage or erosion of bone), persistent urticaria exacerbated by cold and accompanied by hypocomplementemia and progressive cardiac valvular disease with mitral valve regurgitation. There are only three reports described previously documenting five patients with this rare combination of manifestations.

Key Words: hypocomplementemic urticarial vasculitis • Jaccoud's arthropathy • valvular heart disease

Lupus, Vol. 17, No. 9, 837-841 (2008)
DOI: 10.1177/0961203308090113


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