Tubulointerstitial nephritis with uveitis (TINU): A syndrome rheumatologists should recognize - A case report and review of the literature

被引:7
|
作者
Kadanoff, R
Lipps, B
Khanna, A
Hou, S
机构
[1] Loyola Univ, Ctr Med, Dept Med, Rheumatol Sect, Maywood, IL 60153 USA
[2] Loyola Univ, Nephrol Sect, Dept Med, Maywood, IL 60153 USA
[3] Loyola Univ, Dept Surg, Sect Ophthalmol, Maywood, IL 60153 USA
关键词
interstitial nephritis; uveitis; autoimmune disease;
D O I
10.1097/01.rhu.0000111313.32464.a6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with uveitis such as the patient whose case is reported here are often referred to rheurnatologists for investigation of possible underlying systemic diseases. This patient presented with decreased vision, photophobia, weight loss, and fevers and was found to have uveitis, elevated creatinine, and interstitial nephritis. This raised consideration of a variety of systemic diseases before she was determined to have the tubulointerstitial nephritis with uveitis (TINU) syndrome. The TINU syndrome, although known to some ophthalmologists and nephrologists, is still rather obscure. Uncommon but not rare with 133 cases in the literature, TINU syndrome should be one more diagnosis to be considered in patients with uveitis. The median age of onset is 15, but it ranges from 9 to 74. There is a 3:1 female preponderance. Response to corticosteroids, which are used in 80% of reported cases, is rapid. The prognosis for the renal disorder is excellent, although the uveitis often recurs or remains chronic.
引用
收藏
页码:25 / 27
页数:3
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