Hypocomplementemic Urticarial Vasculitis Syndrome with Membranous Nephropathy: Case Report
نویسندگان
چکیده
منابع مشابه
Hypocomplementemic Urticarial Vasculitis Syndrome with Membranous Nephropathy: Case Report
Urticarial vasculitis is a rare disorder that principally manifests with recurrent urticarial, sometimes hemorrhagic, skin lesions and/or angioedema. Its clinical presentation is not always limited to cutaneous lesions and it can potentially affect other organs, such as the joints, lungs, kidneys, and eyes. Systemic involvement can either be present at the onset of disease or develop over time....
متن کاملHypocomplementemic urticarial vasculitis syndrome: an interdisciplinary challenge.
BACKGROUND Chronic urticaria often points the way to the diagnosis of a systemic disease, particularly when urticarial vasculitis can be demonstrated. Hypocomplementemic urticarial vasculitis syndrome (HUVS) is considered to be an independent immunological disease. METHOD Selective literature review and consideration of the author's own clinical experience. RESULTS AND CONCLUSIONS The main ...
متن کاملA Case of Crescentic Glomerulonephritis Complicated with Hypocomplementemic Urticarial Vasculitis Syndrome and ANCA-Associated Vasculitis
Systemic urticaria in a 64-year-old woman was diagnosed as leukocytoclastic vasculitis by a punch biopsy of the skin. Her physical findings improved after prescription of prednisolone at a dose of 20 mg/day, but the skin rash relapsed with renal dysfunction, proteinuria, and hematuria when the dose of prednisolone was reduced over a period of 9 months to 1 mg/day. She was admitted to our instit...
متن کاملHypocomplementemic Urticarial Vasculitis in Systemic Lupus Erythematosus
Urticarial vasculitis is characterized clinically by urticarial skin lesions and histologically by leukocytoclastic vasculitis. Hypocomplementemic urticarial vasculitis is associated with connective tissue diseases such as systemic lupus erythematosus (SLE). We report a case of urticarial vasculitis that preceded manifestations of SLE.
متن کاملPReS-FINAL-2359: Renal involvement in hypocomplementemic urticarial vasculitis syndrome (huvs): report of 3 paediatric cases
Introduction HUVS is a rare disease characterized by persistent urticarial lesions with histological evidence of leucocytoclastic vasculitis and complement activation with a marked decrease in circulating C1q levels. HUVS can present systemic features involving the musculoskeletal, pulmonary, renal and gastrointestinal systems; its peak incidence is in the fifth decade of life. The exact preval...
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ژورنال
عنوان ژورنال: Journal of Korean Medical Science
سال: 2017
ISSN: 1011-8934,1598-6357
DOI: 10.3346/jkms.2017.32.12.2064