Joppich R, Anders D, Eife R, Lampert F
Z Kinderheilkd. 1975;119(3):161-7. doi: 10.1007/BF00445023.
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.
报告一例15岁慢性自身免疫性溶血性贫血男孩，脾切除术后3年出现肾功能不全。经皮肾活检显示为间质性肾炎，伴有明显的淋巴细胞浸润和硬化性肾小球。皮质类固醇治疗后肾脏症状迅速消失。肾脏病变被认为是自身免疫性疾病的一部分。
