Abstract
A 17-year-old boy presented to the emergency room with a 48-hour history of deterioration in the vision of his right eye. Visual acuity was measured at 6/24 in the right eye and 6/6 in the left eye. In the right eye, a small subhyaloid hemorrhage and an associated vitreous hemorrhage were noted. During the next month, the preretinal hemorrhage cleared, revealing a vascularized chorioretinal granuloma in the superotemporal quadrant. A serous retinal detachment with marked retinal exudate was evident, indicating that the lesion was active (Panel A). A physical examination showed no other abnormalities, and the patient's history was unremarkable . . .
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