[Infection-associated Acute Posterior Multifocal Placoid Pigment Epitheliopathy].

[Infection-associated Acute Posterior Multifocal Placoid Pigment Epitheliopathy].

Klin Monbl Augenheilkd. 2017 Apr 04;:

Authors: Jordan F, Voigt U, Dawczynski J, Augsten R, Meller D

Abstract
Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a rare inflammatory chorioretinopathy, which mainly affects young light-skinned, myopic adults between 20 and 30 years of age. The exact aetiology of APMPPE is unknown. Some patients report a viral or flu-like illness preceding the onset of APMPPE symptoms. This condition is usually bilateral and self-limiting with a good overall prognosis. Visual loss is sudden, but usually temporary. Relapses are very rare. Foveal involvement may lead to a worse visual prognosis. There is no current consensus on treatment. A wait-and-see approach with monitoring at short intervals is often sufficient. Based on a case example from our clinic we will demonstrate symptoms, diagnostic work-up and treatment options.

PMID: 28376557 [PubMed - as supplied by publisher]

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