COMPLEJO HOSPITALARIO UNIVERSITARIO DE ALBACETE VogtKoyaganiHarada Syndrome Importance
COMPLEJO HOSPITALARIO UNIVERSITARIO DE ALBACETE Vogt-Koyagani-Harada Syndrome: Importance of early recognition and treatment Denisse Espinosa Encalada Mº Antonia Fagúndez Vargas Raquel Maroto Cejudo Sergio Copete Piqueras
CASE REPORT Medical Record • CC: A healthy 51 -year-old female. Blurry vision, metamorphopsia perception in both eyes (OU). Nausea and frontal headache associated. Eye examination • BCVA: 20/50 in right eye (OD) and 20/30 in left eye (OS) • Eye examination: Anterior Acute Uveitis OU. Bilateral posterior pole serous retinal detachment and papillitis observed in funduscopy.
• • CASE REPORT: TEST Optic disc hyperfluorescence Focal areas of delayed choroidal perfusion No posterior scleritis Multifocal areas of pinpoint leakage Serous detachments with late pooling of dye AF PROTEIN: 0, 52 g/L LUMBAR PUNCTURE ECO Differential Diagnosis NORMAL BRAIN CT CHEST X-RAY LABORATORY, SEROLOGY, AUTOINMUNITY HLA B-27+
CASE REPORT: EVOLUTION OCT, AF LUMBAR PUNCTURE BRAIN CT CHEST X-RAY ECO LABORATORY, SEROLOGY, AUTOINMUNITY INCOMPLETE VOGTKOYAGANIHARADA SYNDROME ORAL PREDNISONE 30 MG DAYLY
CASE REPORT: EVOLUTION & CONCLUSIONS 8 weeks OD OI “A suitable differential diagnosis and an early therapeutic intervention are fundamental to lead a good course of this rare disease”
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