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Benign childhood epilepsy with centrotemporal spikes: an ictal EEG
G M A S Tedrus1, L C Fonseca, D P Castilho
1Department of Neurology, PUC-Campinas, School of Medicine, Pontifícia Universidade Católica de Campinas, Brazil. gmtedrus@.uol.com.br
Insights
Benign childhood epilepsy with centrotemporal spikes (BECTS) seizures were recorded via EEG in an 8-year-old boy. The EEG captured specific spike patterns and slow waves during a 46-second epileptic event.
Area of Science:
- Pediatric Neurology
- Clinical Neurophysiology
Background:
- Benign childhood epilepsy with centrotemporal spikes (BECTS) is a common epilepsy syndrome in children.
- Few electroencephalogram (EEG) seizure recordings exist for BECTS, limiting understanding of its ictal characteristics.
Observation:
- An 8-year-old boy with normal development experienced oropharyngeal seizures during wakefulness and sleep.
- EEG during wakefulness showed spikes in temporal and central regions.
- EEG during sleep captured a 46-second seizure with evolving spike-wave discharges, slow waves, and amplitude changes, predominantly in the right centrotemporal region.
Findings:
- The seizure involved specific EEG patterns: increased spikes, slow waves, decreased amplitude, rhythmic discharges, and high-amplitude spikes.
- Clinical manifestations included clonic lip movements and throat noises, with the mouth shut.
- The child remained asleep and showed no postictal symptoms.
Implications:
- This detailed EEG seizure recording provides valuable insights into BECTS ictal activity.
- Observed EEG patterns, while sharing similarities with other BECTS recordings, also show unique features.
- These differences may reflect variations in the underlying electrical generators within the brain.
Abstract:
Benign childhood epilepsy with centrotemporal spikes (BECTS) is common during childhood, but there are few reports in the literature recording the EEG during a seizure. We studied an 8-year-old boy with oropharyngeal seizures during wakefulness and sleep. Both his neuropsychomotor development and neurological examination were normal. While awake, the subjects's electroencephalogram (EEG) showed normal background activity and epileptiform activity characterized by spikes in the temporal regions (mid and anterior), central region of the right cerebral hemisphere and in the median central and parietal regions. During sleep, his EEG recorded an epileptic seizure that lasted 46 seconds. In the initial phase, the EEG showed an increase in the number of spikes with higher potential in the median central and parietal regions, followed by slow waves associated with the increase in slow waves in the right hemisphere. This was followed by a brief decrease in amplitude of the background activity, and then by rhythmic, diffuse discharges predominantly in the right centrotemporal region, of sharp waves at 12-13 Hz, with increasing potential. Slow waves of high amplitude then occurred for 5 seconds, and finally very high potential spikes reappeared in the central and temporal regions of the right cerebral hemisphere with normalization of the background activity. During these critical phases of the EEG, clonic lip movements and pouting could be observed with the mouth locked shut, associated with "throat noises," but there were no other motor manifestations. The child did not wake up during the seizure and there were no postictal signs or symptoms. Although there are some aspects in common in recordings of BECTS seizures, such as a reduction in amplitude followed by rhythmic discharges of increasing amplitude, differences exist that possibly correspond to the diverse characteristics of the electrical generators.
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