Multimodal Imaging of Atypical Acute Posterior Multifocal Placoid Pigment Epitheliopathy

M. Bouladi, R. Bouraoui, B. Benromdhane, R. Limaiem, F. Mghaieth, L. Elmatri
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Abstract

We present a 52 years-old woman who developed acute posterior multifocal placoid pigment epitheliopathy (APMPPE) with atypical features. APMPPE was unilateral and associated with serous retinal detachment and disc edema causing severe vision loss to 20/400. Oral corticosteroid therapy was prescribed with rapid resolution of lesions and visual improvement to 20/20. Clinical course and multimodal imaging in illustrating different features provide us clues for the definitive diagnosis.
非典型急性后部多灶性Placoid色素上皮病的多模式成像
我们报告了一位52岁的女性,她发展为急性后灶性多灶性placoid pigment epithelial opathy (APMPPE),具有非典型特征。APMPPE是单侧的,伴有浆液性视网膜脱离和椎间盘水肿,导致严重的视力下降至20/400。口服皮质类固醇治疗,病灶迅速消退,视力改善至20/20。临床过程和多模态影像显示不同的特征,为明确诊断提供线索。
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