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Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report
BACKGROUND: Limbic encephalitis is characterized by rapid onset of working memory deficit, mood changes, and often seizures. The condition has a strong paraneoplastic association, but not all cases are invariably due to tumors. CASE PRESENTATION: We present a case of limbic encephalitis in a Chinese...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276199/ https://www.ncbi.nlm.nih.gov/pubmed/30509326 http://dx.doi.org/10.1186/s13256-018-1893-7 |
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author | Cheung, Stephanie S. L. Lau, Gary K. K. Chan, Koon-Ho Wong, Ian Y. H. Lai, Jimmy S. M. Tang, Wai Kiu Shih, Kendrick C. |
author_facet | Cheung, Stephanie S. L. Lau, Gary K. K. Chan, Koon-Ho Wong, Ian Y. H. Lai, Jimmy S. M. Tang, Wai Kiu Shih, Kendrick C. |
author_sort | Cheung, Stephanie S. L. |
collection | PubMed |
description | BACKGROUND: Limbic encephalitis is characterized by rapid onset of working memory deficit, mood changes, and often seizures. The condition has a strong paraneoplastic association, but not all cases are invariably due to tumors. CASE PRESENTATION: We present a case of limbic encephalitis in a Chinese patient who initially presented to our hospital with optic neuritis and no other neurological symptoms. The diagnosis was made radiologically, and cognitive and neurological symptoms did not occur until 5 months later. Extensive investigations for autoimmune, infective, and neoplastic causes were all negative. A working diagnosis of paraneoplastic neurological syndrome was made, and the patient is being managed with high-dose steroid therapy according to the Optic Neuritis Treatment Trial protocol during relapses, as well as with tumor surveillance. CONCLUSIONS: This case highlights ocular symptoms as important clues for diagnosing neurological diseases, as well as autoimmune encephalitis as an important differential diagnosis in the management of “idiopathic” optic neuritis in the Chinese population. |
format | Online Article Text |
id | pubmed-6276199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62761992018-12-06 Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report Cheung, Stephanie S. L. Lau, Gary K. K. Chan, Koon-Ho Wong, Ian Y. H. Lai, Jimmy S. M. Tang, Wai Kiu Shih, Kendrick C. J Med Case Rep Case Report BACKGROUND: Limbic encephalitis is characterized by rapid onset of working memory deficit, mood changes, and often seizures. The condition has a strong paraneoplastic association, but not all cases are invariably due to tumors. CASE PRESENTATION: We present a case of limbic encephalitis in a Chinese patient who initially presented to our hospital with optic neuritis and no other neurological symptoms. The diagnosis was made radiologically, and cognitive and neurological symptoms did not occur until 5 months later. Extensive investigations for autoimmune, infective, and neoplastic causes were all negative. A working diagnosis of paraneoplastic neurological syndrome was made, and the patient is being managed with high-dose steroid therapy according to the Optic Neuritis Treatment Trial protocol during relapses, as well as with tumor surveillance. CONCLUSIONS: This case highlights ocular symptoms as important clues for diagnosing neurological diseases, as well as autoimmune encephalitis as an important differential diagnosis in the management of “idiopathic” optic neuritis in the Chinese population. BioMed Central 2018-12-03 /pmc/articles/PMC6276199/ /pubmed/30509326 http://dx.doi.org/10.1186/s13256-018-1893-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Cheung, Stephanie S. L. Lau, Gary K. K. Chan, Koon-Ho Wong, Ian Y. H. Lai, Jimmy S. M. Tang, Wai Kiu Shih, Kendrick C. Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
title | Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
title_full | Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
title_fullStr | Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
title_full_unstemmed | Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
title_short | Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
title_sort | optic neuritis as the initial clinical presentation of limbic encephalitis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276199/ https://www.ncbi.nlm.nih.gov/pubmed/30509326 http://dx.doi.org/10.1186/s13256-018-1893-7 |
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