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Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis

Vascular occlusive crisis with a concurrent vision loss on both eyes is one of the most devastating disability for sickle cell disease patients. Reportedly occlusive crisis in the eyes is usually temporary whereas if not appropriately managed can result in permanent vision loss. A carefully managed...

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Autores principales: Renganathan, Gowri, Natarajan, Piruthiviraj, Ruck, Lela, Prieto, Roberto, Prakash, Bharat Ved, Thangarasu, Sudhagar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236833/
https://www.ncbi.nlm.nih.gov/pubmed/34176298
http://dx.doi.org/10.1177/23247096211028392
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author Renganathan, Gowri
Natarajan, Piruthiviraj
Ruck, Lela
Prieto, Roberto
Prakash, Bharat Ved
Thangarasu, Sudhagar
author_facet Renganathan, Gowri
Natarajan, Piruthiviraj
Ruck, Lela
Prieto, Roberto
Prakash, Bharat Ved
Thangarasu, Sudhagar
author_sort Renganathan, Gowri
collection PubMed
description Vascular occlusive crisis with a concurrent vision loss on both eyes is one of the most devastating disability for sickle cell disease patients. Reportedly occlusive crisis in the eyes is usually temporary whereas if not appropriately managed can result in permanent vision loss. A carefully managed sickle cell crisis could prevent multiple disabilities including blindness and stroke. We report a case of a 24-year-old female with a history of sickle cell disease who had acute bilateral vision loss during a sickle crisis and recovered significantly with a timely emergent erythrocytapheresis.
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spelling pubmed-82368332021-07-08 Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis Renganathan, Gowri Natarajan, Piruthiviraj Ruck, Lela Prieto, Roberto Prakash, Bharat Ved Thangarasu, Sudhagar J Investig Med High Impact Case Rep Case Report Vascular occlusive crisis with a concurrent vision loss on both eyes is one of the most devastating disability for sickle cell disease patients. Reportedly occlusive crisis in the eyes is usually temporary whereas if not appropriately managed can result in permanent vision loss. A carefully managed sickle cell crisis could prevent multiple disabilities including blindness and stroke. We report a case of a 24-year-old female with a history of sickle cell disease who had acute bilateral vision loss during a sickle crisis and recovered significantly with a timely emergent erythrocytapheresis. SAGE Publications 2021-06-26 /pmc/articles/PMC8236833/ /pubmed/34176298 http://dx.doi.org/10.1177/23247096211028392 Text en © 2021 American Federation for Medical Research https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Renganathan, Gowri
Natarajan, Piruthiviraj
Ruck, Lela
Prieto, Roberto
Prakash, Bharat Ved
Thangarasu, Sudhagar
Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis
title Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis
title_full Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis
title_fullStr Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis
title_full_unstemmed Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis
title_short Concurrent Bilateral Central Retinal Artery Occlusion Secondary to Sickle Cell Crisis
title_sort concurrent bilateral central retinal artery occlusion secondary to sickle cell crisis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236833/
https://www.ncbi.nlm.nih.gov/pubmed/34176298
http://dx.doi.org/10.1177/23247096211028392
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