Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a rare inflammatory eye disease, affecting the inner choroid and the outer retina. Recent advances in multimodal imaging have been important in the understanding of the pathophysiology of the disease, allowing a better characterization of the morphology of this condition. Narrative review. In this review, a comprehensive overview of clinical features, imaging findings, treatment management, and long-term outcomes of patients with APMPPE will be provided. Although APMPPE was originally believed to be a self-limited condition with a good prognosis, the disease can be recurrent and result in significant loss of vision function. Fundus imaging plays an important role in the diagnosis and management of the disease, allowing to evaluate response to treatment and onset of complications.

中文翻译：

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急性后多灶性板状色素上皮病 (APMPPE)

急性后部多灶性血小板色素上皮病 (APMPPE) 是一种罕见的炎症性眼病，影响内脉络膜和外视网膜。多模态成像的最新进展对于了解该疾病的病理生理学非常重要，可以更好地表征这种疾病的形态。叙事评论。在这篇综述中，将全面概述 APMPPE 患者的临床特征、影像学发现、治疗管理和长期结果。虽然 APMPPE 最初被认为是一种预后良好的自限性疾病，但该疾病可能会复发并导致视力功能显着丧失。眼底成像在疾病的诊断和管理中起着重要作用，可以评估对治疗的反应和并发症的发生。