Take a closer look at TINU syndrome; analysis of a case

Q4 Medicine Journal of Nephropathology Pub Date : 2022-06-28 DOI:10.34172/jnp.2022.17349
Eduarda Carias, A. Cabrita, P. Neves, A. P. Silva
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Abstract

Tubulointerstitial nephritis and uveitis syndrome (TINU) combines tubulointerstitial nephritis and uveitis and is a known cause of kidney failure in children and adults. This is a challenging diagnosis since renal and ocular manifestations may not occur simultaneously and may be present in several alternative diagnosis. The authors report the case of a 28-year-old patient with acute kidney injury (AKI) and biopsy-proven acute tubulointerstitial nephritis. Bilateral symptomatic uveitis presented six months after the initial presentation. Physicians in charge of patients with kidney disease attributed to acute tubulointerstitial nephritis must bear in mind the need for ophthalmologic surveillance for at least one year post-diagnosis. Although a diagnosis of exclusion, its incidence may be higher than described. Kidney disease is believed to be self-limited and prognosis still, most patients will require systemic therapy and relapses are common.
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仔细看看TINU综合症;案例分析
管间质性肾炎和葡萄膜炎综合征(TINU)合并管间质性肾炎和葡萄膜炎,是儿童和成人肾衰竭的已知原因。这是一个具有挑战性的诊断,因为肾脏和眼部表现可能不会同时发生,并可能出现在几个替代诊断。作者报告了一例28岁的急性肾损伤(AKI)患者,活检证实急性肾小管间质性肾炎。双侧症状性葡萄膜炎在初次出现6个月后出现。负责急性肾小管间质性肾炎肾病患者的医生必须牢记,诊断后至少一年需要进行眼科监测。虽然诊断排除,其发生率可能高于描述。肾脏疾病被认为是自限性和预后仍然,大多数患者将需要全身治疗和复发是常见的。
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来源期刊
Journal of Nephropathology
Journal of Nephropathology Medicine-Nephrology
CiteScore
1.30
自引率
0.00%
发文量
35
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