Sjögren's Reticular Retinal Dystrophy
Journal of the Korean Ophthalmological Society
; : 887-891, 2019.
Article
de Ko
| WPRIM
| ID: wpr-766908
Bibliothèque responsable:
WPRO
ABSTRACT
PURPOSE: To report a rare case of Sjögren's reticular retinal dystrophy. CASE SUMMARY: 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.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Rétine
/
Rétinal
/
Troubles de la vision
/
Angiographie fluorescéinique
/
Néovascularisation choroïdienne
/
Tomographie par cohérence optique
/
Épithélium pigmentaire de la rétine
/
Dystrophies rétiniennes
/
Dégénérescence maculaire
Limites du sujet:
Humans
/
Male
langue:
Ko
Texte intégral:
Journal of the Korean Ophthalmological Society
Année:
2019
Type:
Article