Purpose: Operculo-insular seizures are heterogeneous and may resemble seizures originating from the temporal, frontal, or parietal lobe. Although surface and invasive EEG recordings are often necessary to detect operculo-insular seizures, electrophysiological features of operculo-insular epilepsies remain poorly characterized. This study describes the EEG findings of patients with operculo-insular epilepsy.
Methods: We reviewed electrophysiological data of all patients (n = 9) with operculo-insular seizures revealed by intracranial EEG and for whom operculo-insular epilepsy was confirmed by good seizure outcome after resective or radiosurgery at our center between 2005 and 2013. Patients were divided according to whether their seizure focus involved the anterior (group 1; n = 4) or posterior (group 2; n = 5) portion of the insula.
Results: Interictal scalp EEG was lateralizing and showed distinct topographical spike patterns between groups: frontal and temporal in group 1, temporal in group 2. Intracranial recordings showed abundant spikes limited to the operculo-insular region or involving distant areas in the frontal/temporal (group 1) and temporal/parietal lobes (group 2). Ictal intracranial EEG revealed discharges limited to the insula or simultaneously involving extrainsular contacts at onset, notably the orbitofrontal cortex (group 1) and the frontal and parietal opercula (group 2), and propagating to the frontal and temporal lobes in group 1 and to parietal and temporal lobes in group 2.
Conclusions: Spike distribution and seizure propagation in operculo-insular epilepsy follows an anterior-to-posterior pattern mirroring an anterior or posterior insular focus localization. When presented with frontal and/or temporal epileptiform abnormalities, an operculo-insular focus should be considered.
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http://dx.doi.org/10.1097/WNP.0000000000000391 | DOI Listing |
Epileptic Disord
December 2024
Neurophysiology Unit, Neurology Department, Unidade Local de Saúde São João, Porto, Portugal.
Postictal paresis ("Todd's paralysis") is commonly observed as a unilateral, transient motor weakness, lasting minutes to hours, after focal or focal to bilateral tonic-clonic seizures, contralateral to the epileptogenic zone. Bilateral postictal paresis is exceedingly rare and could be misinterpreted, especially if the preceding convulsive phase was not witnessed. An 18-year-old right-handed male patient with refractory focal epilepsy with seizure onset at age 3 years, was admitted for presurgical video-EEG monitoring.
View Article and Find Full Text PDFFront Neurol
July 2024
Sherbrooke Connectivity Imaging Lab (SCIL), Sherbrooke University, Sherbrooke, QC, Canada.
Introduction: Operculo-insular epilepsy (OIE) is a rare condition amenable to surgery in well-selected cases. Despite the high rate of neurological complications associated with OIE surgery, most postoperative deficits recover fully and rapidly. We provide insights into this peculiar pattern of functional recovery by investigating the longitudinal reorganization of structural networks after surgery for OIE in 10 patients.
View Article and Find Full Text PDFClin EEG Neurosci
March 2024
APHM, Timone Hospital, Epileptology Department, Member of the ERN EpiCARE, Marseille, France.
We present a case of a patient with focal non-motor emotional seizures with dacrystic expression in the context of drug-resistant magnetic resonance imaging negative epilepsy. The pre-surgical evaluation suggested a hypothesis of a right fronto-temporal epileptogenic zone. Stereoelectroencephalography recorded dacrystic seizures arising from the right anterior operculo-insular () area with secondary propagation to temporal and parietal cortices during the dacrystic behavior.
View Article and Find Full Text PDFBrain Sci
January 2022
University of Montreal Health Center Research Center (CRCHUM), 900 St.-Denis Street, Montreal, QC H2X 0A9, Canada.
Background: Epilepsy surgery failure is not uncommon, with several explanations having been proposed. In this series, we detail cases of epilepsy surgery failure subsequently attributed to insular involvement.
Methods: We retrospectively identified patients investigated at the epilepsy monitoring units of two Canadian tertiary care centers (2004-2020).
Clin Neurophysiol
December 2021
Institute of Neuroscience (IoNS), Université Catholique de Louvain, Brussels, Belgium; Centre for Refractory Epilepsy, Department of Neurology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Objective: To evaluate the accuracy of automatedinterictallow-density electrical source imaging (LD-ESI) to define the insular irritative zone (IZ) by comparing the simultaneous interictal ESI localization with the SEEG interictal activity.
Methods: Long-term simultaneous scalp electroencephalography (EEG) and stereo-EEG (SEEG) with at least one depth electrode exploring the operculo-insular region(s) were analyzed. Automated interictal ESI was performed on the scalp EEG using standardized low-resolution brain electromagnetic tomography (sLORETA) and individual head models.
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