A case of acute posterior multifocal placoid pigment epitheliopathy was evaluated over a 22-month period. Various pathologic stages are illustrated by color photographs and fluorescein angiography. Our studies of this patient include electroretinography, electro-oculography, dark adaptation, and color vision. These indicate that the anomaly is most consistent with a diffuse disease of the pigment epithelium.
Fishman GA, Rabb MF, Kaplan J. Acute Posterior Multifocal Placoid Pigment Epitheliopathy. Arch Ophthalmol. 1974;92(2):173–177. doi:10.1001/archopht.1974.01010010179021
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