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Epilepsy surgery in patient with monogenic epilepsy related to SCN8A mutation.

Authors :
Podkorytova I
Hays R
Perven G
Alick Lindstrom S
Source :
Epilepsy & behavior reports [Epilepsy Behav Rep] 2022 Mar 22; Vol. 18, pp. 100536. Date of Electronic Publication: 2022 Mar 22 (Print Publication: 2022).
Publication Year :
2022

Abstract

Epilepsy surgery is superior to prolonged medical therapy in patients with drug-resistant focal epilepsy, but reports on epilepsy surgery outcomes for patients with a genetic etiology are limited, especially in adults. This is the first documented report of a stereoelectroencephalography (SEEG) evaluation and resective surgery outcome in an adult patient with epilepsy related to SCN8A mutation. We describe a patient with epilepsy related to SCN8A mutation which was reported as a variant of uncertain significance at time of his pre-surgical evaluation and reclassified as likely pathogenic about 3 years after resective epilepsy surgery. Most of his pre-surgical evaluation results suggested right temporal lobe epilepsy, but few reported semiological symptoms, ictal SPECT, and neuropsychology results were discordant, and brain MRI was non-lesional. Therefore, SEEG was recommended; ultimately, seizures were localized to the right hippocampus. He was seizure-free for 1.5 years after right anterior temporal lobectomy, then reported three focal to bilateral tonic-clonic (FBTC) seizures in the subsequent 12 months (preoperatively, 6 focal impaired awareness seizures and 4-6 FBTC per year). This case demonstrates that epilepsy surgery reduced seizure burden in a patient with SCN8A-related epilepsy granting him short-term seizure freedom after resection, and then decreased seizure frequency after relapse compared to the preoperative baseline.<br />Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (© 2022 The Author(s).)

Details

Language :
English
ISSN :
2589-9864
Volume :
18
Database :
MEDLINE
Journal :
Epilepsy & behavior reports
Publication Type :
Academic Journal
Accession number :
35492509
Full Text :
https://doi.org/10.1016/j.ebr.2022.100536