Igarashi T, Kawato H, Kamoshita S, Nosaka K, Seiya K, Hayakawa H
Department of Paediatrics, Faculty of Medicine, University of Tokyo, Japan.
Pediatr Nephrol. 1992 Nov;6(6):547-9. doi: 10.1007/BF00866499.
We describe an 11-year-old male patient with acute tubulointerstitial nephritis with uveitis (TINU) syndrome. He presented with easy fatigability, pallor, nocturia and weight loss. Laboratory examination disclosed anaemia, polyclonal hypergammaglobulinaemia, low molecular weight proteinuria, glycosuria, aminoaciduria, proximal and distal renal tubular acidosis, a urine concentration defect and decreased creatinine clearance. The multiple renal tubular dysfunction and slight glomerular dysfunction subsided spontaneously. Bilateral anterior uveitis was manifested 7 months after the onset of the disease. This is the first reported case of TINU syndrome with multiple proximal and distal tubular dysfunction including a complete type of Fanconi's syndrome.
我们描述了一名患有急性肾小管间质性肾炎伴葡萄膜炎(TINU)综合征的11岁男性患者。他表现为易疲劳、面色苍白、夜尿和体重减轻。实验室检查发现贫血、多克隆高球蛋白血症、低分子量蛋白尿、糖尿、氨基酸尿、近端和远端肾小管酸中毒、尿浓缩功能缺陷以及肌酐清除率降低。多种肾小管功能障碍和轻微的肾小球功能障碍自发缓解。双侧前葡萄膜炎在疾病发作7个月后出现。这是首例报道的伴有多种近端和远端肾小管功能障碍(包括完全型范科尼综合征)的TINU综合征病例。