Objective To report posterior sympathetic ophthalmia in North Indian population as an early manifestation of sympathetic ophthalmia.MethodsForty consecutive patients with a diagnosis of sympathetic ophthalmia seen between 1989 and 2004 at our centre were studied for their clinical presentation and disease course. All received systemic corticosteroids and 12 patients, in addition, also received immunosuppressive agents.ResultsThere were 28 male and 12 female patients with a median age of 29.4 years. In 22 of the 40 sympathizing eyes, the only presenting sign was the fundus lesions without any associated anterior segment inflammation. Only four eyes showed classically described granulomatous anterior uveitis at presentation. The fundus lesions predominately included exudative retinal detachment (29 eyes), yellowish-white mid-peripheral lesions (10 eyes), optic disc oedema (15 eyes), vasculitis (three eyes), and peripapillary choroidal neovascular membrane (two eyes). Over a median follow-up of 5.2 years, recurrences were seen in 12 of 40 (30%) eyes and were mainly in the anterior segment. Over a median follow-up of 5.2 years, a final visual acuity of 20/40 or better could be achieved in 29/36 (80.5%) eyes.ConclusionIn the early stage, sympathetic ophthalmia may present only in the posterior segment without any associated anterior segment inflammation and carries a good visual prognosis. Anterior segment inflammation, however, maybe seen during recurrences. © 2008 Macmillan Publishers Limited. All rights reserved.
CITATION STYLE
Gupta, V., Gupta, A., & Dogra, M. R. (2008). Posterior sympathetic ophthalmia: A single centre long-term study of 40 patients from North India. Eye, 22(12), 1459–1464. https://doi.org/10.1038/sj.eye.6702927
Mendeley helps you to discover research relevant for your work.