Acute posterior multifocal placoid pigment epitheliopathy (Q88392): Difference between revisions

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Uveíte inflamatória que pertence ao grupo heterogêneo das síndromes dos pontos brancos, nas quais lesões claras começam a se formar na mácula, dentro da retina do olho. Com o tempo, as lesões causam perda de visão que pode variar de leve a grave, mas sem envolvimento de dor. Classificadas como um transtorno inflamatório que é agudo, mas autolimitado, as lesões deixam alguma pigmentação, mas a acuidade visual melhora eventualmente.
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This is an inflammatory uveitis that belongs to the heterogenous group of white dot syndromes in which light-coloured lesions begin to form in the macula, inside the retina of the eye. Over time, the lesions cause vision loss that can go from mild to severe, but with no pain involved. Classified as an inflammatory disorder that is acute, but self-limiting, the lesions leave behind some pigmentation, but visual acuity eventually improves.

Revision as of 14:35, 15 August 2026

This is an inflammatory uveitis that belongs to the heterogenous group of white dot syndromes in which light-coloured lesions begin to form in the macula, inside the retina of the eye. Over time, the lesions cause vision loss that can go from mild to severe, but with no pain involved. Classified as an inflammatory disorder that is acute, but self-limiting, the lesions leave behind some pigmentation, but visual acuity eventually improves.
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ID_2036282532
    English
    Acute posterior multifocal placoid pigment epitheliopathy
    This is an inflammatory uveitis that belongs to the heterogenous group of white dot syndromes in which light-coloured lesions begin to form in the macula, inside the retina of the eye. Over time, the lesions cause vision loss that can go from mild to severe, but with no pain involved. Classified as an inflammatory disorder that is acute, but self-limiting, the lesions leave behind some pigmentation, but visual acuity eventually improves.

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