IgA Glomerulonephritis with Irregular IntramembranousDense Deposits

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Abstract

A 30-year-old white male presented with hematuria, proteinuria and normal renal function following a flu-like illness. IgA was mildly elevated but C3 and C4 levels were normal in serum. Renal biopsy showed a mesangial proliferative nephritis with immunohistochemical features of IgA nephritis but with an unusual pattern and distribution of deposits in glomerular, tubular and Bowman’s capsular basement membranes.

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Brief report: heavy-chain deposition disease.

P Aucouturier, Thomas Martin, J Preud'homme … (1993)

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Journal

Journal ID (publisher-id): NEF

Journal ID (nlm-ta): Nephron

Journal ID (doi): 10.1159/issn.1660-8151

Title: Nephron

Publisher: S. Karger AG

ISSN (Print): 1660-8151

ISSN (Electronic): 2235-3186

Publication date Subscription-year: 1998

Publication date (Print): November 1998

Publication date (Electronic): 02 November 1998

Volume: 80

Issue: 3

Pages: 340-343

Affiliations

The Toronto Hospital, Western Division and Scarborough Centenary Health Centre, Toronto, Ont., Canada

Article

Publisher ID: 45195 Other ID: Nephron 1998;80:340–343

DOI: 10.1159/000045195

PubMed ID: 9807044

SO-VID: 5fdd75c9-534f-4ede-9093-7772aad6ab71

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IgA Glomerulonephritis with Irregular IntramembranousDense Deposits

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Abstract

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Karger: Nephrology

Most cited references 1

Brief report: heavy-chain deposition disease.

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