2007
DOI: 10.1038/sj.eye.6702927
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Posterior sympathetic ophthalmia: a single centre long-term study of 40 patients from North India

Abstract: Objective To report 'posterior sympathetic ophthalmia' in North Indian population as an early manifestation of sympathetic ophthalmia. Methods Forty 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. Results There were 28 male and 12 female patients with a median age of 29.4 years. In 22… Show more

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Cited by 51 publications
(61 citation statements)
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“…However, several new studies have indicated that this description may represent just one part of the entire disease spectrum. Retinal involvement in the form of exudative retinal detachment, yellow-white mid-peripheral nodules, disc edema, vasculitis, peripapillary subretinal neovascularization and APMPPE-like lesions with exudative retinal detachment has been reported in several clinical studies using the term posterior sympathetic ophthalmia for cases with predominant retinal involvement [2,9,10]. It has also been speculated that the posterior form of the disease may actually be the early stage of sympathetic ophthalmia.…”
Section: Discussionmentioning
confidence: 95%
See 1 more Smart Citation
“…However, several new studies have indicated that this description may represent just one part of the entire disease spectrum. Retinal involvement in the form of exudative retinal detachment, yellow-white mid-peripheral nodules, disc edema, vasculitis, peripapillary subretinal neovascularization and APMPPE-like lesions with exudative retinal detachment has been reported in several clinical studies using the term posterior sympathetic ophthalmia for cases with predominant retinal involvement [2,9,10]. It has also been speculated that the posterior form of the disease may actually be the early stage of sympathetic ophthalmia.…”
Section: Discussionmentioning
confidence: 95%
“…We found that classic presentation was rather uncommon in the majority of our patients who presented with posterior sympathetic ophthalmia with minimal/no anterior segment inflammation [2]. The fundus lesions at presentation in our series included exudative retinal detachment, yellow-white midperipheral nodules, disc edema, vasculitis, peripapillary subretinal neovascularization and acute posterior multifocal placoid pigment epitheliopathy (APMPPE)-like lesions with exudative retinal detachment associated with minimal or no anterior segment inflammation and vitritis [2].…”
Section: Introductionmentioning
confidence: 93%
“…Initial anterior segment changes can sometimes be absent and SO may present with posterior segment findings only. In a very recent report of 40 consecutive patients from India [19], 22 patients presented with fundus lesions without any accompanying anterior segment finding. Although the most common inciting event was trauma, 10 exciting eyes had undergone surgery; two of which had scleral buckle with subretinal fluid drainage and two had PPV.…”
Section: Discussionmentioning
confidence: 96%
“…The clinical appearance of SO varies within a mild to severe range. In a long-term study of Gupta et al, the most important posterior segment manifestations were exudative retinal detachment in the majority of patients, Dalen-Fuchs nodules, papillitis, and vasculitis as secondary events [ 103 ]. The complications of chronic infl ammation include secondary glaucoma, cataract, and chronic maculopathy.…”
Section: Clinical Symptoms and Signsmentioning
confidence: 98%
“…The complications of chronic infl ammation include secondary glaucoma, cataract, and chronic maculopathy. Misdiagnosis and inappropriate treatment of this condition may result in severe infl ammatory sequela such as retinal and optic atrophy, infl ammatory choroidal neovascularization (CNV), choroidal atrophy, and phthisis bulbi [ 103 ]. Rarely, SO may be associated with the typical extraocular fi ndings accompanying Vogt-Koyanagi-Harada syndrome, such as alopecia, vitiligo, cells in the cerebrospinal fl uid, and dysacousia.…”
Section: Clinical Symptoms and Signsmentioning
confidence: 99%