Possible Tubulointerstitial Nephritis and Uveitis (TINU) syndrome

Shruti Kochar, S. Lahane, P. Mahendradas, Rwituja Thomas
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Abstract

Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare form of ocular inflammation, with the only systemic manifestation being acute interstitial nephritis. We report a case of TINU that presented with ocular abnormalities after being diagnosed with interstitial nephritis. Our patient had an initial presentation of fever with chills and weakness at the time of presentation to their nephrologist. Blood investigations revealed elevated creatinine, proteinuria and increased β2 microglobulin, following which they were diagnosed with possible TINU syndrome as per Mandeville's diagnostic criteria. Our patients responded well to oral and topical steroids. She had recurrent episodes, which were subsequently managed. It is important to have a high index of suspicion for TINU as patients, even in the absence of a renal biopsy, as they have an excellent prognosis with timely treatment. TINU is a rare diagnosis and is most likely because it is often missed. However, patients with TINU syndrome require a customized multispecialty approach in order to diagnose, rule out other causes of uveitis and AIN and hence manage appropriately.
可能的输卵管间质性肾炎和葡萄膜炎(TINU)综合征
小管间质性肾炎和葡萄膜炎(TINU)综合征是一种罕见的眼部炎症,唯一的全身表现是急性间质性肾小球肾炎。我们报告了一例TINU,在诊断为间质性肾炎后出现眼部异常。我们的患者在向肾脏科医生就诊时,最初表现为发烧、发冷和虚弱。血液检查显示肌酐升高、蛋白尿和β2微球蛋白增加,随后根据Mandeville的诊断标准,他们被诊断为可能的TINU综合征。我们的患者对口服和外用类固醇反应良好。她反复发作,后来得到了治疗。作为患者,即使在没有肾活检的情况下,对TINU也要有很高的怀疑指数,这一点很重要,因为及时治疗可以获得良好的预后。TINU是一种罕见的诊断,很可能是因为它经常被遗漏。然而,TINU综合征患者需要一种定制的多专科方法来诊断、排除葡萄膜炎和AIN的其他原因,从而进行适当的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
18 weeks
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