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Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview

False lateralization of ictal onset by scalp electroencephalogram (EEG) is an infrequent entity that has been reported in patients with mesial temporal lobe epilepsy associated with hippocampal sclerosis (HS). In these cases, a tendency for rapid seizures that spread through the frontal-limbic syste...

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Autores principales: Gaviria Carrillo, Mariana, López, Jonathan, Rodríguez Q., Jesús H., Gaona, Ivan, Ortiz-Guerrero, Gloria, Nava-Mesa, Mauricio O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565586/
https://www.ncbi.nlm.nih.gov/pubmed/32846994
http://dx.doi.org/10.3390/brainsci10090584
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author Gaviria Carrillo, Mariana
López, Jonathan
Rodríguez Q., Jesús H.
Gaona, Ivan
Ortiz-Guerrero, Gloria
Nava-Mesa, Mauricio O.
author_facet Gaviria Carrillo, Mariana
López, Jonathan
Rodríguez Q., Jesús H.
Gaona, Ivan
Ortiz-Guerrero, Gloria
Nava-Mesa, Mauricio O.
author_sort Gaviria Carrillo, Mariana
collection PubMed
description False lateralization of ictal onset by scalp electroencephalogram (EEG) is an infrequent entity that has been reported in patients with mesial temporal lobe epilepsy associated with hippocampal sclerosis (HS). In these cases, a tendency for rapid seizures that spread through the frontal-limbic system and hippocampal commissural pathways to the contralateral hemisphere has been proposed. Cerebral cavernous malformations (CCMs), which constitute a collection of abnormally configured small blood vessels with irregular structures, is a well-defined epilepsy-associated pathology. Their primary association with seizures might be explained either as a result of physiological changes affecting the cerebral cortex immediately surrounding the CCM (an epileptogenic mechanism that is relevant for both, temporal and extratemporal lesions) or as a result of promoting epileptogenicity in remote but anatomo-functionally connected brain regions, a mechanism that is particularly relevant for temporal lobe lesions. To date, there have been only two publications on falsely lateralizing ictal onsets by EEG in temporal cavernoma, but not in other regions. Here, we report a rare case of apparent false lateralization of ictal onset by scalp EEG in a patient with a left medial frontal gyrus cavernoma (supplementary motor area), and discuss some relevant pathophysiological mechanisms of false lateralization.
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spelling pubmed-75655862020-10-26 Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview Gaviria Carrillo, Mariana López, Jonathan Rodríguez Q., Jesús H. Gaona, Ivan Ortiz-Guerrero, Gloria Nava-Mesa, Mauricio O. Brain Sci Case Report False lateralization of ictal onset by scalp electroencephalogram (EEG) is an infrequent entity that has been reported in patients with mesial temporal lobe epilepsy associated with hippocampal sclerosis (HS). In these cases, a tendency for rapid seizures that spread through the frontal-limbic system and hippocampal commissural pathways to the contralateral hemisphere has been proposed. Cerebral cavernous malformations (CCMs), which constitute a collection of abnormally configured small blood vessels with irregular structures, is a well-defined epilepsy-associated pathology. Their primary association with seizures might be explained either as a result of physiological changes affecting the cerebral cortex immediately surrounding the CCM (an epileptogenic mechanism that is relevant for both, temporal and extratemporal lesions) or as a result of promoting epileptogenicity in remote but anatomo-functionally connected brain regions, a mechanism that is particularly relevant for temporal lobe lesions. To date, there have been only two publications on falsely lateralizing ictal onsets by EEG in temporal cavernoma, but not in other regions. Here, we report a rare case of apparent false lateralization of ictal onset by scalp EEG in a patient with a left medial frontal gyrus cavernoma (supplementary motor area), and discuss some relevant pathophysiological mechanisms of false lateralization. MDPI 2020-08-24 /pmc/articles/PMC7565586/ /pubmed/32846994 http://dx.doi.org/10.3390/brainsci10090584 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Gaviria Carrillo, Mariana
López, Jonathan
Rodríguez Q., Jesús H.
Gaona, Ivan
Ortiz-Guerrero, Gloria
Nava-Mesa, Mauricio O.
Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview
title Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview
title_full Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview
title_fullStr Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview
title_full_unstemmed Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview
title_short Apparent False Lateralization of Seizure Onset by Scalp EEG in Temporal Lobe Epilepsy Associated with Cerebral Cavernous Malformation: A Case Report and Overview
title_sort apparent false lateralization of seizure onset by scalp eeg in temporal lobe epilepsy associated with cerebral cavernous malformation: a case report and overview
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565586/
https://www.ncbi.nlm.nih.gov/pubmed/32846994
http://dx.doi.org/10.3390/brainsci10090584
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