Article ID Journal Published Year Pages File Type
3045711 Clinical Neurophysiology 2011 5 Pages PDF
Abstract

ObjectiveThe aim of this study was to evaluate the relationship between semiology of seizures in children and adolescents to the corresponding EEG localization.MethodsCharts of 225 consecutive pediatric epilepsy patients undergoing Video-EEG monitoring (VEM) over 2 years were reviewed. Seizure semiology recorded during VEM was classified according to ILAE seizure semiology terminology and EEG localization, and analyzed based on onset as defined by the EEG data (generalized, frontal, temporal, parietal, occipital or multilobar).ResultsA total of 1008 seizures were analyzed in 225 children (mean age 8.5 years, range 0–20), with 50% boys. Auras and seizures with automatisms arose predominantly from the temporal lobes (p < 0.001). Tonic, clonic and tonic-clonic seizures had most commonly generalized onset (p < 0.001). Hypomotor seizures were most frequently seen from the frontal lobes (p < 0.001). Hypermotor seizures had most commonly temporal lobe or multiple lobe onset (p < 0.001 and p < 0.05 respectively). Atonic, myoclonic seizures and epileptic spasms had almost exclusively a generalized onset (p < 0.001).ConclusionsDifferent seizure semiologies relate to specific brain regions, with overlap between focal and generalized semiological seizure types, as identified electrographically.SignificanceSemiology of seizures can provide important information for epilepsy localization, and should not be overlooked, especially in patients undergoing pre-surgical evaluation. Separation of clinical seizure description and EEG findings may be useful, in particular when only incomplete information is available. i.e. during the first office visit.

► On examination of seizure semiology and EEG localization we did not find a one-to-one relationship. ► Different seizure semiologies relate to specific brain regions, but this relationship is not exclusive. ► Our findings support the recent separation of seizure semiology and epilepsy localization by the ILAE.

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