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Vol.46 No.4 >

Please use this identifier to cite or link to this item: http://hdl.handle.net/10564/941

Title: 尋常性乾癬を合併したIgA腎症の1例
Other Titles: A CASE OF IGA NEPHROPATHY COMPLICATED BY PSORIASIS VULGARIS
Authors: 松村, 典彦
花谷, 正和
西野, 俊彦
椎木, 英夫
土肥, 和紘
村松, 勉
白井, 利彦
Keywords: IgA nephropathy
psoriasis vulgaris
serum IgA level
Issue Date: 31-Aug-1995
Publisher: 奈良医学会
奈良県立医科大学
Citation: 奈良医学雑誌 Vol.46 No.4 p.286-293
Abstract: A 55-year-old male patient presenting with psoriasis vulgaris and IgA nephropathy is reported. He was first noticed to have. proteinuria on an annual medical checkup at his company in 1979. Although proteinuria has been detected at every medical opportunity, he had never undergone closer evaluation. Scaly erythema on the right forehead had appeared since October 1984 and was diagnosed as psoriasis vulgaris by means of skin biopsy. In March 1985, he developed hypertension and was treated with antihyper- tensive drug by his family physician. Urinalysis showed proteinuria, hematuria and some hyaline casts. A 24-h urine collection contained 1.2g protein. Renal function test on admission was normal ; serum creatinine, 0.9mg/dl, creatinine clearance, 91ml/min. Immunoserological tests demonstrated that autoantibodies, serum complement titers and circulatory immune complexes (Clq binding assay) were all negative or within normal limits, except for the increase in serum IgA of 592mg/dl. The renal biopsy revealed diffuse mesangial proliferative glomerulonephritis. Immunofluorescence microscopy disclosed diffuse mesangial staining for IgA and C3. The diagnosis of IgA nephropathy was made. In spite of anti-platelet and anti-hypertensive therapy, his renal function gradually deteriorated over 8 years. Skin lesions still remain with remission and exacerbation. We discuss the relationship between IgA nephropathy and psoriasis vulgaris in this paper with reference to the literature.
URI: http://hdl.handle.net/10564/941
ISSN: 04695550
13450069
Appears in Collections:Vol.46 No.4

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