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VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report
Anti-NMDA receptor encephalitis (ANRE) has been previously reported as a rare cause of nonconvulsive status epilepticus (NCSE). Vagus nerve stimulation (VNS) is generally considered as a palliative treatment for patients with drug-resistant partial-onset epilepsy. Here, we report a case of refractor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436507/ https://www.ncbi.nlm.nih.gov/pubmed/26005636 http://dx.doi.org/10.1016/j.ebcr.2015.02.003 |
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author | Alsaadi, Taoufik Shakra, Mustafa Turkawi, Lamya Hamid, Jassin |
author_facet | Alsaadi, Taoufik Shakra, Mustafa Turkawi, Lamya Hamid, Jassin |
author_sort | Alsaadi, Taoufik |
collection | PubMed |
description | Anti-NMDA receptor encephalitis (ANRE) has been previously reported as a rare cause of nonconvulsive status epilepticus (NCSE). Vagus nerve stimulation (VNS) is generally considered as a palliative treatment for patients with drug-resistant partial-onset epilepsy. Here, we report a case of refractory NCSE that was terminated after vagus nerve stimulator implantation. To our knowledge, similar cases have not been reported previously. |
format | Online Article Text |
id | pubmed-4436507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-44365072015-05-23 VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report Alsaadi, Taoufik Shakra, Mustafa Turkawi, Lamya Hamid, Jassin Epilepsy Behav Case Rep Case Report Anti-NMDA receptor encephalitis (ANRE) has been previously reported as a rare cause of nonconvulsive status epilepticus (NCSE). Vagus nerve stimulation (VNS) is generally considered as a palliative treatment for patients with drug-resistant partial-onset epilepsy. Here, we report a case of refractory NCSE that was terminated after vagus nerve stimulator implantation. To our knowledge, similar cases have not been reported previously. Elsevier 2015-05-15 /pmc/articles/PMC4436507/ /pubmed/26005636 http://dx.doi.org/10.1016/j.ebcr.2015.02.003 Text en © 2015 The Authors 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 Alsaadi, Taoufik Shakra, Mustafa Turkawi, Lamya Hamid, Jassin VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report |
title | VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report |
title_full | VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report |
title_fullStr | VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report |
title_full_unstemmed | VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report |
title_short | VNS terminating refractory nonconvulsive SE secondary to anti-NMDA encephalitis: A case report |
title_sort | vns terminating refractory nonconvulsive se secondary to anti-nmda encephalitis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436507/ https://www.ncbi.nlm.nih.gov/pubmed/26005636 http://dx.doi.org/10.1016/j.ebcr.2015.02.003 |
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