Sjögren's Reticular Retinal Dystrophy
Journal of the Korean Ophthalmological Society
;
: 887-891, 2019.
Artículo
en Coreano
| WPRIM
| ID: wpr-766908
ABSTRACT
PURPOSE:
To report a rare case of Sjögren's reticular retinal dystrophy. CASESUMMARY:
A 54-year-old male presented with blurred vision and metamorphopsia in both eyes since a few years prior to his initial visit. There was a bilateral reticular network of yellow deposits throughout the posterior pole on fundus examination, which was hyperautofluorescent in fundus autofluorescence photographs. The pigment alterations were more visible with fluorescein angiography, which showed hypofluorescent lesions with hyperfluorescent borders. Spectral-domain optical coherence tomography showed elevations of the outer retina associated with the presence of subretinal hyperreflective material. Based on the conclusive correlation with clinical features, we diagnosed Sjögren's reticular retinal dystrophy.CONCLUSIONS:
Sjögren's reticular retinal dystrophy is characterized by its specific pigment changes at the level of clinical manifestations and the retinal pigment epithelium. In cases of Sjögren's reticular retinal dystrophy, close monitoring is required because it has a lifetime risk of choroidal neovascularization.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Retina
/
Retinaldehído
/
Trastornos de la Visión
/
Angiografía con Fluoresceína
/
Neovascularización Coroidal
/
Tomografía de Coherencia Óptica
/
Epitelio Pigmentado de la Retina
/
Distrofias Retinianas
/
Degeneración Macular
Límite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
2019
Tipo del documento:
Artículo
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