Subject(s)
Acquired Immunodeficiency Syndrome/complications , Chorioretinitis/complications , Neurosyphilis/complications , Retinal Necrosis Syndrome, Acute/complications , Acquired Immunodeficiency Syndrome/drug therapy , Adult , Anti-Inflammatory Agents/therapeutic use , Candidiasis, Oral/complications , Candidiasis, Oral/drug therapy , Chorioretinitis/drug therapy , Ethylenediamines/therapeutic use , Fluorescein Angiography , Fundus Oculi , HIV Seropositivity/complications , Humans , Lichenoid Eruptions/complications , Lichenoid Eruptions/drug therapy , Male , Neurosyphilis/drug therapy , Penicillin G/therapeutic use , Penicillins/therapeutic use , Retinal Necrosis Syndrome, Acute/drug therapy , Scleritis/complications , Scleritis/drug therapy , SteroidsABSTRACT
BACKGROUND: Intermediate uveitis is characterized by vitreal inflammation with associated inflammation of the vitreous base and peripheral anterior retina and choroid. It may be found as an isolated and idiopathic condition or in association with systemic disorders such as multiple sclerosis and sarcoidosis. OBJECTIVE: To identify the clinical features of intermediate uveitis and assess its association with systemic diseases. METHODS: Retrospective study of 83 patients presenting with intermediate uveitis between 1970 and 1991. RESULTS: Evidence of systemic disorders was found in 26 of 83 patients (31.3%). Of these 26 patients, 10 had presumed sarcoidosis, 6 had multiple sclerosis, 2 had isolated optic neuritis, 2 had inflammatory bowel disease, 4 had isolated thyroid abnormalities, and 2 had histories suggestive of Epstein-Barr virus infection. Associated ocular findings included cystoid macular edema, peripheral retinal perivascular sheathing, cataracts, posterior vitreous detachment, fine keratic precipitates, preretinal macular fibrosis, retinal tears, retinal detachment, and optic disc edema. CONCLUSIONS: Patients with intermediate uveitis may have associated systemic diseases and should have careful follow-up with regular systemic evaluation.
