| Literature DB >> 1079992 |
R Joppich, D Anders, R Eife, F Lampert.
Abstract
A case is reported of a 15-year-old boy with chronic autoimmune hemolytic anemia who developed renal insufficiency 3 years after splenectomy. An interstitial nephritis with striking lymphocytic infiltrates and sclerosed glomeruli could be demonstrated by percutaneous renal biopsy. Renal symptoms disappeared promptly after corticosteroid therapy. The renal lesions are thought to have arisen as part of the autoimmune disease.Entities:
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Year: 1975 PMID： 1079992 DOI： 10.1007/bf00445023
Source DB: PubMed Journal: Z Kinderheilkd ISSN： 0044-2917