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Ocular Toxoplasmosis

Also known as: Toxoplasma Retinochoroiditis

Ocular toxoplasmosis is necrotizing retinochoroiditis caused by Toxoplasma gondii. It is the most common infectious cause of posterior uveitis worldwide. Seroprevalence is 30 to 50% globally, and ocular disease is highest in southern Brazil, where up to about 18% of seropositive people have lesions.

Infection is congenital or acquired (from undercooked meat, contaminated water or vegetables, or oocysts from cat feces). Ocular disease follows reactivation of bradyzoite cysts in a retinal scar, producing a fresh lesion adjacent to old pigmentation (a satellite lesion). Recurrence is common (about 50% within 3 years). Congenital disease is bilateral in 40 to 60%. Immunocompromised patients show extensive, multifocal necrosis without a scar.

Without treatment active lesions heal over 6 to 8 weeks. Complications: macular scarring, choroidal neovascularization, retinal detachment, optic neuropathy, vascular occlusion and glaucoma.

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