Matsumoto K, Katayama H, Hatano M
Second Department of Internal Medicine, Nihon University School of Medicine, Tokyo, Japan.
Nephron. 1988;49(3):251-4. doi: 10.1159/000185065.
A 29-year-old Japanese male with a 19-year history of subcutaneous eosinophilic lymphoid granuloma (Kimura's disease) was referred to the Nephrology Service of the Nihon University Hospital for evaluation of edema and massive proteinuria. The renal biopsy disclosed minimal glomerular lesions. In this paper a case of nephrotic syndrome associated with eosinophilic lymphoid granuloma is reported.
一名患有皮下嗜酸性淋巴肉芽肿（木村病）19年的29岁日本男性，因水肿和大量蛋白尿被转诊至日本大学医院肾病科进行评估。肾活检显示肾小球病变轻微。本文报告一例与嗜酸性淋巴肉芽肿相关的肾病综合征病例。
