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Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions

A previously healthy 22-year-old African American woman presented with bilateral vision loss associated with headache. Her ocular examination was significant for bilateral retinal arterial “boxcarring,” retinal whitening, retinal hemorrhages, and cherry red spots. She was diagnosed with bilateral ce...

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Detalles Bibliográficos
Autores principales: Saraf, Steven S., Patel, Yogin P., Desai, Ankit, Desai, Uday R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333186/
https://www.ncbi.nlm.nih.gov/pubmed/25722904
http://dx.doi.org/10.1155/2015/206906
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author Saraf, Steven S.
Patel, Yogin P.
Desai, Ankit
Desai, Uday R.
author_facet Saraf, Steven S.
Patel, Yogin P.
Desai, Ankit
Desai, Uday R.
author_sort Saraf, Steven S.
collection PubMed
description A previously healthy 22-year-old African American woman presented with bilateral vision loss associated with headache. Her ocular examination was significant for bilateral retinal arterial “boxcarring,” retinal whitening, retinal hemorrhages, and cherry red spots. She was diagnosed with bilateral central retinal artery occlusions and was hospitalized due to concomitant diagnosis of stroke and hypercoagulable state. She was also found to be in heart failure and kidney failure. Rheumatology was consulted and she was diagnosed with catastrophic antiphospholipid syndrome in association with systemic lupus erythematosus. Approximately 7 months after presentation, the patient's vision improved and remained stable at 20/200 and 20/80.
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spelling pubmed-43331862015-02-26 Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions Saraf, Steven S. Patel, Yogin P. Desai, Ankit Desai, Uday R. Case Rep Ophthalmol Med Case Report A previously healthy 22-year-old African American woman presented with bilateral vision loss associated with headache. Her ocular examination was significant for bilateral retinal arterial “boxcarring,” retinal whitening, retinal hemorrhages, and cherry red spots. She was diagnosed with bilateral central retinal artery occlusions and was hospitalized due to concomitant diagnosis of stroke and hypercoagulable state. She was also found to be in heart failure and kidney failure. Rheumatology was consulted and she was diagnosed with catastrophic antiphospholipid syndrome in association with systemic lupus erythematosus. Approximately 7 months after presentation, the patient's vision improved and remained stable at 20/200 and 20/80. Hindawi Publishing Corporation 2015 2015-02-02 /pmc/articles/PMC4333186/ /pubmed/25722904 http://dx.doi.org/10.1155/2015/206906 Text en Copyright © 2015 Steven S. Saraf et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Saraf, Steven S.
Patel, Yogin P.
Desai, Ankit
Desai, Uday R.
Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions
title Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions
title_full Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions
title_fullStr Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions
title_full_unstemmed Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions
title_short Catastrophic Antiphospholipid Syndrome Presenting as Bilateral Central Retinal Artery Occlusions
title_sort catastrophic antiphospholipid syndrome presenting as bilateral central retinal artery occlusions
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333186/
https://www.ncbi.nlm.nih.gov/pubmed/25722904
http://dx.doi.org/10.1155/2015/206906
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