Carvalho Madalena, Galhardo Saraiva Francisca, Coutinho Inês, Bento Vanda, Cabral Marta
Pediatric Service, Child and Youth Department, Hospital Professor Doutor Fernando Fonseca, Lisboa, PRT.
Ophthalmology Service, Hospital Professor Doutor Fernando Fonseca, Lisboa, PRT.
Cureus. 2024 Aug 7;16(8):e66380. doi: 10.7759/cureus.66380. eCollection 2024 Aug.
Tubulointerstitial nephritis and uveitis syndrome (TINU) is a rare autoimmune disease. It is characterized by uveitis and kidney damage. The presentation of uveitis is typically anterior and bilateral, while the renal lesion is an acute interstitial nephritis. We report a case of an adolescent diagnosed with this disease, who presented with ocular and constitutional symptoms. An ophthalmologic examination confirmed the diagnosis of uveitis, and subsequent systemic evaluation revealed impaired renal function. The findings of the renal biopsy established the diagnosis after ruling out other systemic diseases. Given the rarity and nonspecific clinical presentation of this condition, a high level of suspicion is required for early diagnosis and treatment. Clinicians should consider this diagnosis in a pediatric patient with uveitis and impaired renal function.
肾小管间质性肾炎和葡萄膜炎综合征(TINU)是一种罕见的自身免疫性疾病。其特征为葡萄膜炎和肾脏损害。葡萄膜炎的表现通常为前部且双侧性,而肾脏病变为急性间质性肾炎。我们报告一例被诊断为此病的青少年病例,该患者出现了眼部和全身症状。眼科检查确诊为葡萄膜炎,随后的全身评估显示肾功能受损。肾活检结果在排除其他全身性疾病后确立了诊断。鉴于这种疾病的罕见性和非特异性临床表现,早期诊断和治疗需要高度怀疑。临床医生应在患有葡萄膜炎和肾功能受损的儿科患者中考虑这一诊断。