Evolving Fuchs’ uveitis - A diagnostic challenge

Abstract

Purpose: To study cases of Fuchs’ uveitis (FU) diagnosed as uveitis other than FU at initial visits. Methods: A retrospective, observational chart review. Details of clinical presentation, initial diagnosis, treatment details, and follow-up before and after the diagnosis of FU was studied. Result: Twenty eyes of 19 patients finally diagnosed with FU. Mean total follow-up was 39 months (range: 3–120 months, median: 30 months) and follow-up after diagnosis of FU was 18 months (range: 0–84 months, median: 11 months). Most of the cases were diagnosed with anterior plus intermediate uveitis at the presentation (n = 8, 42.1%) and received steroid treatment. Keratic precipitates (KPs) typical of FU developed after mean 5.4 months of presentation (range: 1–18 months, median: 2 months). Altered iris pattern was noted after 17 months of presentation (range: 2–70 months, median: 8.5). Vitritis of grades 1–2 was present in all eyes. Overlap of uveitis of other etiology (retinal vasculitis, presumed tubercular intermediate uveitis) was found in three patients. Systemic immune disease (systemic lupus erythematosus, pulmonary sarcoidosis) was present in two patients. No treatment for the ocular inflammation was given after the diagnosis of FU in any patient and no change in the pattern of FU was observed during further follow-up. Conclusion: Evolving FU may lead to misdiagnosis and mismanagement. We suggest a conservative approach, withholding steroid treatment, allowing FU to evolve, in otherwise asymptomatic patients with white eye, mild to moderate anterior chamber (AC) and vitreous inflammation, absent posterior synechiae and normal fundus examination or fundus examination suggestive of resolved uveitis.