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Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome
Cerebral hyperperfusion syndrome (CHS) is a rare life-threatening complication of carotid endarterectomy (CEA) and carotid artery stenting (CAS) for carotid artery stenosis. The incidence varies between 0 and 3%, depending on the severity of the stenosis, perioperative hypertension, and contralatera...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442331/ https://www.ncbi.nlm.nih.gov/pubmed/28573058 http://dx.doi.org/10.1155/2017/7965758 |
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author | Kurukumbi, Mohankumar Truong, Ahn Pirsaharkhiz, Naghemeh |
author_facet | Kurukumbi, Mohankumar Truong, Ahn Pirsaharkhiz, Naghemeh |
author_sort | Kurukumbi, Mohankumar |
collection | PubMed |
description | Cerebral hyperperfusion syndrome (CHS) is a rare life-threatening complication of carotid endarterectomy (CEA) and carotid artery stenting (CAS) for carotid artery stenosis. The incidence varies between 0 and 3%, depending on the severity of the stenosis, perioperative hypertension, and contralateral carotid stenosis. This case report reports a 53-year-old female patient presenting with decreased alertness and multiple tonic-clonic seizures, in the background of bilateral CEA. She was found to have bilateral carotid stenosis. Her left CEA was performed three months prior and right CEA was four days prior to her current presentation with seizures. After bilateral CEA, the imaging showed extensive pathologic process involving primarily the subcortical white matter and overlying cortex, more on the right cerebral hemisphere. On follow-up six weeks later, she reported no recurrent seizures and imaging showed decrease in abnormal signal intensity of the grey and white matter. This was indicative of near complete resolution of hyperperfusion damage. CHS is a rare complication due to the loss of autoregulation of the cerebrovascular system and increased blood flow status after bilateral CEA. This case is reported because of a rare and unique presentation of seizures in the background of bilateral CEA. |
format | Online Article Text |
id | pubmed-5442331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54423312017-06-01 Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome Kurukumbi, Mohankumar Truong, Ahn Pirsaharkhiz, Naghemeh Case Rep Neurol Med Case Report Cerebral hyperperfusion syndrome (CHS) is a rare life-threatening complication of carotid endarterectomy (CEA) and carotid artery stenting (CAS) for carotid artery stenosis. The incidence varies between 0 and 3%, depending on the severity of the stenosis, perioperative hypertension, and contralateral carotid stenosis. This case report reports a 53-year-old female patient presenting with decreased alertness and multiple tonic-clonic seizures, in the background of bilateral CEA. She was found to have bilateral carotid stenosis. Her left CEA was performed three months prior and right CEA was four days prior to her current presentation with seizures. After bilateral CEA, the imaging showed extensive pathologic process involving primarily the subcortical white matter and overlying cortex, more on the right cerebral hemisphere. On follow-up six weeks later, she reported no recurrent seizures and imaging showed decrease in abnormal signal intensity of the grey and white matter. This was indicative of near complete resolution of hyperperfusion damage. CHS is a rare complication due to the loss of autoregulation of the cerebrovascular system and increased blood flow status after bilateral CEA. This case is reported because of a rare and unique presentation of seizures in the background of bilateral CEA. Hindawi 2017 2017-05-10 /pmc/articles/PMC5442331/ /pubmed/28573058 http://dx.doi.org/10.1155/2017/7965758 Text en Copyright © 2017 Mohankumar Kurukumbi et al. https://creativecommons.org/licenses/by/4.0/ 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 Kurukumbi, Mohankumar Truong, Ahn Pirsaharkhiz, Naghemeh Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome |
title | Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome |
title_full | Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome |
title_fullStr | Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome |
title_full_unstemmed | Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome |
title_short | Uncommon Etiology for Seizure: Cerebral Hyperperfusion Syndrome |
title_sort | uncommon etiology for seizure: cerebral hyperperfusion syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442331/ https://www.ncbi.nlm.nih.gov/pubmed/28573058 http://dx.doi.org/10.1155/2017/7965758 |
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