Abstract

Purpose: To report a case of biopsy-proven tubulointerstitial nephritis and uveitis (TINU) syndrome involving the posterior segment. Method: Case report. Results: A 29-year-old male had suffered from painless blurred vision in the left eye for one week. The patient had the history of bilateral anterior uveitis. Initially, his best spectacle corrected visual acuity (BSCVA) was 20/20 in the right eye and 20/40 in the left eye. The ocular examination revealed cells and flares in the bilateral anterior chambers. Fundus examination showed macular exudates, intraretinal hemorrhage, sheathing of retinal vessels, and optic disc edema. Laboratory tests revealed elevated serum creatinine (3.8 mg/dl) and lood urea nitrogen (BUN) (48.3 mg/dl). Percutaneous renal biopsy showed cute tubulointerstitial nephritis. In addition, we excluded other diseases which an cause both acute nephritis and uveitis, such as Sjogren syndrome, ehcet' disease and systemic lupus erythematosus (SLE). The diagnosis of ubulointerstitial nephritis and uveitis syndrome was established. The patient as treated with topical prednisolone and cycloplegics. Intravenous pulse therapy of methylprednisolone (1 gm daily) was also given for three days, followed by oral prednisolone 60 mg daily. Ocular inflammation and optic disc edema in both eyes were resolved and BSCVA of 20/20 was achieved in the left eye after six-month follow-up. Conclusion: TINU syndrome is probably an under-diagnosed cause of uveitis. Ophthalmologists play an important role in the initial discovery of patients with TINU syndrome. A thorough medical evaluation of any patient presenting with uveitis and systemic disease is crucial to early diagnosis and appropriate management.

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