Yao Y-H, Lin C-C, Chung Y-M, Yang A-H, Li S-Y, Lin C-C, Lin Y-P, Yang W-C, Yang C-Y
Division of Nephrology, Department of Medicine, , National Yang-Ming University, Taipei, Taiwan.
Clin Nephrol. 2011 Feb;75 Suppl 1:75-8. doi: 10.5414/cn106471.
We report a 57-year-old woman with concurrent tubulointerstitial nephritis and uveitis syndrome (TINU) and Fanconi's syndrome. She presented with sudden onset of bilateral ocular pain, blurred vision, acute renal failure, glucosuria and proteinuria. Slit lamp examination revealed acute bilateral anterior uveitis. Tubulointerstitial nephritis was confirmed by kidney biopsy. Laboratory examination revealed normoglycemic glucosuria, proteinuria, normal anion-gap metabolic acidosis, phosphaturia, urinary uric acid wasting and kaliuresis leading to hypokalemia. Her vision and renal function improved gradually after systemic steroid therapy. There have been rare reports of TINU syndrome which had features of Fanconi's syndrome. The prevalence of TINU syndrome may be underestimated, and its association with Fanconi's syndrome requires further investigation.
我们报告了一名57岁的女性,她同时患有肾小管间质性肾炎和葡萄膜炎综合征(TINU)以及范科尼综合征。她出现双侧眼部疼痛、视力模糊、急性肾衰竭、糖尿和蛋白尿的突然发作。裂隙灯检查显示双侧急性前葡萄膜炎。肾活检证实为肾小管间质性肾炎。实验室检查显示血糖正常性糖尿、蛋白尿、正常阴离子间隙代谢性酸中毒、磷酸盐尿、尿尿酸排泄增多和钾尿导致低钾血症。全身类固醇治疗后,她的视力和肾功能逐渐改善。关于具有范科尼综合征特征的TINU综合征的报道很少。TINU综合征的患病率可能被低估,其与范科尼综合征的关联需要进一步研究。