Kerner Markus, Todoroff Julia, von Schnakenburg Christian, Amann Kerstin, Müller-Kühnle Julian
General Practice, Dr. Kerner's General Medical Practice, Neuffen, DEU.
Pediatrics and Adolescent Medicine, Klinikum Esslingen, Esslingen, DEU.
Cureus. 2025 Aug 2;17(8):e89245. doi: 10.7759/cureus.89245. eCollection 2025 Aug.
Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare autoimmune condition primarily affecting adolescents. Diagnosis is frequently delayed due to the nonspecific and temporally dissociated presentation of renal and ocular symptoms. We report the case of a 15-year-old girl who presented to her general practitioner with fatigue, polyuria, and recent weight loss. Laboratory workup revealed acute kidney injury with elevated serum creatinine and a tubular pattern of proteinuria, prompting timely referral to a pediatric hospital. Renal biopsy confirmed acute, non-granulomatous tubulointerstitial nephritis. Despite lacking ocular complaints, ophthalmologic examination revealed bilateral anterior uveitis, confirming the diagnosis of TINU syndrome. Notably, symptom onset followed the initiation of sertraline, suggesting a potential drug-induced trigger. The patient responded rapidly to high-dose oral corticosteroids, with full recovery of renal function and general well-being. Mild neuropsychiatric side effects occurred during treatment but resolved without intervention. Follow-up was coordinated through pediatric nephrology and ophthalmology. This case highlights the role of primary care in the early recognition of rare systemic diseases. Tubular protein markers proved valuable in characterizing the renal injury pattern. In adolescents with unexplained renal dysfunction and constitutional symptoms, TINU should be part of the differential, even in the absence of visual complaints. Recent medication changes should raise suspicion for drug-induced immune-mediated nephritis.
肾小管间质性肾炎和葡萄膜炎(TINU)综合征是一种罕见的自身免疫性疾病,主要影响青少年。由于肾脏和眼部症状表现不具特异性且在时间上不相关联,诊断常常延迟。我们报告一例15岁女孩,她因疲劳、多尿和近期体重减轻就诊于全科医生。实验室检查显示急性肾损伤,血清肌酐升高,蛋白尿呈肾小管型,促使其及时转诊至儿科医院。肾活检证实为急性非肉芽肿性肾小管间质性肾炎。尽管没有眼部不适主诉,但眼科检查发现双侧前葡萄膜炎,从而确诊为TINU综合征。值得注意的是,症状出现于舍曲林开始使用之后,提示可能是药物诱发。患者对大剂量口服糖皮质激素反应迅速,肾功能和整体健康状况完全恢复。治疗期间出现轻度神经精神副作用,但未干预即自行缓解。后续随访由儿科肾病科和眼科共同协调。该病例凸显了初级保健在早期识别罕见全身性疾病中的作用。肾小管蛋白标志物在明确肾损伤模式方面很有价值。对于有不明原因肾功能不全和全身症状的青少年,即使没有视觉症状,TINU也应列入鉴别诊断。近期用药变化应引起对药物诱发免疫介导性肾炎的怀疑。