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Interstitial nephritis in autoimmune hemolytic anemia
Authors:R. Joppich  D. Anders  R. Eife  F. Lampert
Affiliation:1. H?matologische Abteilung der Universit?ts-Kinderklinik München, München, Germany
2. Institut für Cytobiologie und Cytopathologie der Universit?t Marburg, München, Germany
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.
Keywords:
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