Presumed bilateral cilioretinal artery occlusion related to relapsing white dot syndrome

• Tipo: Artigo em Revista Científica Internacional
• Data: 2016

Autores

Beato, J (Autor) FMUP; Figueira, L (Autor) FMUP; Penas, S (Autor) FMUP; Santos Silva, R (Autor) FMUP; Manuel Falcão (Autor) FMUP; Ângela Carneiro (Autor) FMUP; Falcão-Reis F (Autor) FMUP

Revista

Título: European Journal of Ophthalmology

Vol. 26

Páginas: E118-E120

ISSN: 1120-6721

Editora: WICHTIG PUBLISHING

Indexação

ISI Web of Knowledge - 0 Citações

Scopus - 0 Citações

Outras Informações

ID Authenticus: P-00K-TZW

DOI: 10.5301/ejo.5000778

Abstract (EN): Purpose: To report a presumed case of bilateral asynchronous cilioretinal occlusion associated with white dot syndrome. Methods: A 19-year-old woman presented with decreased vision in the right eye. Cilioretinal occlusion was diagnosed and multimodal imaging was performed. Results: Laboratory workup was negative. Fluorescein and indocyanine green angiography revealed an inflammatory choroidopathy in the right eye. Spectral-domain coherence tomography (OCT) initially showed internal retinal layer edema followed by atrophy in the papillomacular bundle. Left eye presented asymptomatic decreased visual acuity and OCT findings were compatible with previous cilioretinal occlusion. Conclusions: Cilioretinal occlusion findings were present in both eyes. Multimodal fundus imaging allowed idiopathic inflammatory choroidopathy diagnosis in the right eye, suggesting that a recurrent inflammatory process caused an asynchronous vascular occlusion.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 3