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Progressive Susac syndrome with bilateral visual loss and disability
Susac syndrome (SS) is a rare retinal-cochlear-cerebral disease with an unclear etiology. A 35-year-old man presented with sudden painless vision loss in the right eye and 2 months later in the left eye with hemiparesis, behavioral changes, and hearing loss. Ophthalmic examinations revealed multiple...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5151162/ https://www.ncbi.nlm.nih.gov/pubmed/27853020 http://dx.doi.org/10.4103/0301-4738.194334 |
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author | Entezari, Morteza Karimi, Saeed Feizi, Mohammadali |
author_facet | Entezari, Morteza Karimi, Saeed Feizi, Mohammadali |
author_sort | Entezari, Morteza |
collection | PubMed |
description | Susac syndrome (SS) is a rare retinal-cochlear-cerebral disease with an unclear etiology. A 35-year-old man presented with sudden painless vision loss in the right eye and 2 months later in the left eye with hemiparesis, behavioral changes, and hearing loss. Ophthalmic examinations revealed multiple branch retinal artery occlusions (BRAOs) in both eyes. Brain magnetic resonance imaging showed inflammatory changes with multiple “punched-out” lesions in the corpus callosum which confirmed the diagnosis of SS. Despite intravenous and oral corticosteroid therapy, the disease progressed with the development of new BRAOs, low vision in both eyes, and disability. Prompt diagnosis and early treatment may save the vision and even patient's life. |
format | Online Article Text |
id | pubmed-5151162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51511622016-12-20 Progressive Susac syndrome with bilateral visual loss and disability Entezari, Morteza Karimi, Saeed Feizi, Mohammadali Indian J Ophthalmol Brief Communication Susac syndrome (SS) is a rare retinal-cochlear-cerebral disease with an unclear etiology. A 35-year-old man presented with sudden painless vision loss in the right eye and 2 months later in the left eye with hemiparesis, behavioral changes, and hearing loss. Ophthalmic examinations revealed multiple branch retinal artery occlusions (BRAOs) in both eyes. Brain magnetic resonance imaging showed inflammatory changes with multiple “punched-out” lesions in the corpus callosum which confirmed the diagnosis of SS. Despite intravenous and oral corticosteroid therapy, the disease progressed with the development of new BRAOs, low vision in both eyes, and disability. Prompt diagnosis and early treatment may save the vision and even patient's life. Medknow Publications & Media Pvt Ltd 2016-09 /pmc/articles/PMC5151162/ /pubmed/27853020 http://dx.doi.org/10.4103/0301-4738.194334 Text en Copyright: © Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Brief Communication Entezari, Morteza Karimi, Saeed Feizi, Mohammadali Progressive Susac syndrome with bilateral visual loss and disability |
title | Progressive Susac syndrome with bilateral visual loss and disability |
title_full | Progressive Susac syndrome with bilateral visual loss and disability |
title_fullStr | Progressive Susac syndrome with bilateral visual loss and disability |
title_full_unstemmed | Progressive Susac syndrome with bilateral visual loss and disability |
title_short | Progressive Susac syndrome with bilateral visual loss and disability |
title_sort | progressive susac syndrome with bilateral visual loss and disability |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5151162/ https://www.ncbi.nlm.nih.gov/pubmed/27853020 http://dx.doi.org/10.4103/0301-4738.194334 |
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