Cargando…

Central retinal artery occlusion secondary to Barlow's disease

PURPOSE: To report a rare case of isolated, unilateral CRAO in a young patient with mitral valve prolapse secondary to Barlow's disease. OBSERVATIONS: A 29-year-old woman with history of premature ventricular contractions and cardiac ablation presented to the emergency room after sudden onset p...

Descripción completa

Detalles Bibliográficos
Autores principales: Wilkins, Carl S., McCabe, Katherine, Deobhakta, Avnish, Chelnis, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956717/
https://www.ncbi.nlm.nih.gov/pubmed/29780944
http://dx.doi.org/10.1016/j.ajoc.2018.03.003
_version_ 1783323933133504512
author Wilkins, Carl S.
McCabe, Katherine
Deobhakta, Avnish
Chelnis, James
author_facet Wilkins, Carl S.
McCabe, Katherine
Deobhakta, Avnish
Chelnis, James
author_sort Wilkins, Carl S.
collection PubMed
description PURPOSE: To report a rare case of isolated, unilateral CRAO in a young patient with mitral valve prolapse secondary to Barlow's disease. OBSERVATIONS: A 29-year-old woman with history of premature ventricular contractions and cardiac ablation presented to the emergency room after sudden onset painless visual loss in her left eye (OS). Her vision was 20/20 in her right eye and hand motion in the left. Fundus exam demonstrated a central retinal artery occlusion (CRAO) OS. Computerized tomography of head and neck were unremarkable. She underwent cerebral angiogram and local intra-arterial thrombolysis. Her vision remained stable post-procedure, with marked APD and stable fundus examination. Her cardiac work-up revealed a left atrial mass with calcified mitral valve, and small atrial septal defect. Rheumatologic, hematologic, and auto-immune work-up were unremarkable. She underwent resection of the mass with repair of mitral valve and ASD closure. Surgical pathology was compatible with diagnosis of Barlow's disease, a cause of mitral valve prolapse. The patient underwent intravitreal injection of anti-VEGF therapy at one month follow-up, with vision stable at hand motion and without neovascularization on subsequent evaluation. CONCLUSIONS: In young patients presenting with CRAO, aggressive work-up for systemic disease or embolic source must be undertaken to avoid future sequelae.
format Online
Article
Text
id pubmed-5956717
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-59567172018-05-18 Central retinal artery occlusion secondary to Barlow's disease Wilkins, Carl S. McCabe, Katherine Deobhakta, Avnish Chelnis, James Am J Ophthalmol Case Rep Case report PURPOSE: To report a rare case of isolated, unilateral CRAO in a young patient with mitral valve prolapse secondary to Barlow's disease. OBSERVATIONS: A 29-year-old woman with history of premature ventricular contractions and cardiac ablation presented to the emergency room after sudden onset painless visual loss in her left eye (OS). Her vision was 20/20 in her right eye and hand motion in the left. Fundus exam demonstrated a central retinal artery occlusion (CRAO) OS. Computerized tomography of head and neck were unremarkable. She underwent cerebral angiogram and local intra-arterial thrombolysis. Her vision remained stable post-procedure, with marked APD and stable fundus examination. Her cardiac work-up revealed a left atrial mass with calcified mitral valve, and small atrial septal defect. Rheumatologic, hematologic, and auto-immune work-up were unremarkable. She underwent resection of the mass with repair of mitral valve and ASD closure. Surgical pathology was compatible with diagnosis of Barlow's disease, a cause of mitral valve prolapse. The patient underwent intravitreal injection of anti-VEGF therapy at one month follow-up, with vision stable at hand motion and without neovascularization on subsequent evaluation. CONCLUSIONS: In young patients presenting with CRAO, aggressive work-up for systemic disease or embolic source must be undertaken to avoid future sequelae. Elsevier 2018-03-08 /pmc/articles/PMC5956717/ /pubmed/29780944 http://dx.doi.org/10.1016/j.ajoc.2018.03.003 Text en © 2018 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case report
Wilkins, Carl S.
McCabe, Katherine
Deobhakta, Avnish
Chelnis, James
Central retinal artery occlusion secondary to Barlow's disease
title Central retinal artery occlusion secondary to Barlow's disease
title_full Central retinal artery occlusion secondary to Barlow's disease
title_fullStr Central retinal artery occlusion secondary to Barlow's disease
title_full_unstemmed Central retinal artery occlusion secondary to Barlow's disease
title_short Central retinal artery occlusion secondary to Barlow's disease
title_sort central retinal artery occlusion secondary to barlow's disease
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956717/
https://www.ncbi.nlm.nih.gov/pubmed/29780944
http://dx.doi.org/10.1016/j.ajoc.2018.03.003
work_keys_str_mv AT wilkinscarls centralretinalarteryocclusionsecondarytobarlowsdisease
AT mccabekatherine centralretinalarteryocclusionsecondarytobarlowsdisease
AT deobhaktaavnish centralretinalarteryocclusionsecondarytobarlowsdisease
AT chelnisjames centralretinalarteryocclusionsecondarytobarlowsdisease