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Archivos de la Sociedad Española de Oftalmología

versión impresa ISSN 0365-6691

Resumen

DE-DOMINGO, B. et al. Vogt Koyanagi Harada Syndrome. Arch Soc Esp Oftalmol [online]. 2008, vol.83, n.6, pp.385-389. ISSN 0365-6691.

Case reports: Case 1. A female patient with visual loss and migraine who was found to have an exudative, bilateral retinal detachment. Steroid therapy was commenced initially and then cyclosporin-A added. Nine months later, her vision was 10/10 in the right eye and 9/10 in the left eye. Case 2. A female patient with unclear vision who was found to have an exudative, bilateral retinal detachment. Systemic steroid therapy was given and ultimately her vision was 9/10 in the right eye and 8/10 in the left eye. Discussion: Vogt Koyanagi Harada syndrome is a bilateral granulomatous panuveitis associated with neurologic and dermatologic disorders. When a patient has exudative multifocal and bilateral retinal detachment and systemic symptomatology, the possibility of this disease needs to be suspected. Good visual prognosis is possible if early treatment is given.

Palabras clave : Bilateral panuveitis; Harada syndrome; serous detachment; uveomeningoen; Vogt Koyanagi Harada syndrome.

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