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- W2337836498 abstract "Acute posterior multifocal placoid pigment epitheliopathy is an unusual, self-limited, inflammatory disease that affects the choriocapillaris, and external retinal layers. A 26 year-old male patient complained of decreased visual acuity, as well as photopsia in both eyes for the past three days. Best corrected visual acuity was 20/200 in the right eye and 20/80 in the left eye. There was no anterior chamber inflammation or vitritis in either eye. There were plaque-like, cream-coloured sub-retinal lesions with ill-defined borders in the posterior pole of both eyes. Fluorescein angiography showed hypofluorescent lesions in early phases that corresponded to the lesions seen in the clinical examination. These lesions were hyperfluorescent in later phases of the angiography. Based on the clinical and angiographic findings, an acute posterior multifocal placoid pigment epitheliopathy diagnosis was made. Acute posterior multifocal placoid pigment epitheliopathy is an inflammatory condition of unknown origin that is part of the differential diagnosis of placoid retinal diseases. La epiteliopatía pigmentaria placoide multifocal posterior aguda es una entidad poco frecuente, autolimitada, de carácter inflamatorio a nivel de coriocapilaris y capas externas de la retina. Paciente varón de 26 años de edad, que acude por baja visual de inicio repentino en ambos ojos y 3 días de evolución, acompañada de fotopsias. A la exploración se encontró una capacidad visual de 20/200 en el ojo derecho y de 20/80 en el ojo izquierdo. No se encontró reacción inflamatoria en la cámara anterior ni tampoco vitritis en ningún ojo. En el polo posterior se encontraron lesiones de aspecto cremoso blanquecino subretinianas, en forma de placas. En la fluorangiografía retiniana se encontró hipofluorescencia en fases tempranas de las lesiones, vistas en fotos clínicas con hiperfluorescencia en fases tardías. En función de los datos clínicos y angiográficos se diagnosticó como epiteliopatía pigmentaria placoide multifocal posterior aguda. La epiteliopatía pigmentaria placoide multifocal posterior aguda es una entidad inflamatoria de origen desconocido que forma parte del diagnóstico diferencial, de las llamadas enfermedades placoideas de la retina." @default.
- W2337836498 created "2016-06-24" @default.
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- W2337836498 date "2016-03-01" @default.
- W2337836498 modified "2023-09-23" @default.
- W2337836498 title "Acute posterior multifocal placoid pigment epitheliopathy" @default.
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- W2337836498 doi "https://doi.org/10.1016/j.circen.2016.02.011" @default.
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