Nikolić V, Bogdanović R, Ognjanović M, Sindjić M, Popović S
Srp Arh Celok Lek. 1995 Jan-Feb;123(1-2):8-11.
Clinical features and natural course of acute tubulointerstial nephritis and uveitis (TINU syndrome) in five adolescent patients (3 girls and 2 boys), are presented. Initial nonspecific symptoms preceding nephropathy were anorexia, weight loss, fever and malaise. Inflammatory syndrome consisted of increased ESR, high plasma proteins and gamma globulins. Analysis of urine showed proteinuria and sterile leukocyturia. Laboratory features of tubular dysfunction and decreased GFR were found in all patients. Renal biopsy, which was performed in 2 pts, revealed acute interstitial nephritis. Anterior uveitis which appeared later, was successfully treated with topical steroids. Renal function completely recovered within a few month in four pts and markedly improved in one. Despite the fact that renal biopsy was not performed in all children, the combination of an acute nonoliguric renal failure without hypertension and signs of tubular dysfunction together with particular benign course, suggested acute idiopathic TINU syndrome.
本文介绍了5例青少年患者(3名女孩和2名男孩)的急性肾小管间质性肾炎和葡萄膜炎(TINU综合征)的临床特征及自然病程。肾病前期最初的非特异性症状为厌食、体重减轻、发热和不适。炎症综合征表现为血沉加快、血浆蛋白和γ球蛋白升高。尿液分析显示蛋白尿和无菌性白细胞尿。所有患者均发现肾小管功能障碍和肾小球滤过率降低的实验室特征。2例患者进行了肾活检,结果显示为急性间质性肾炎。后来出现的前葡萄膜炎经局部使用类固醇成功治疗。4例患者的肾功能在几个月内完全恢复,1例患者明显改善。尽管并非所有儿童都进行了肾活检,但急性非少尿性肾衰竭且无高血压、伴有肾小管功能障碍体征以及特别良性的病程,提示为急性特发性TINU综合征。