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Sensorimotor seizures of pediatric onset with unusual posteriorly oriented rolandic spikes
Yosuke Kakisaka1, Nobukazu Nakasato, Kazuhiro Haginoya
1Department of Pediatrics, Tohoku University School of Medicine, Sendai, Miyagi, Japan.
Insights
This study identifies a rare form of childhood epilepsy characterized by sensorimotor seizures and posteriorly oriented rolandic discharges, distinct from typical benign childhood epilepsy.
Area of Science:
- Neurology
- Epileptology
- Pediatric Neurology
Background:
- Benign childhood epilepsy with centro-temporal spikes (BECCT) typically presents with anteriorly oriented rolandic discharges.
- This study investigates an atypical presentation of childhood-onset epilepsy featuring sensorimotor seizures and posteriorly oriented rolandic discharges.
Purpose of the Study:
- To characterize a rare epilepsy syndrome in children with sensorimotor seizures and posteriorly oriented rolandic discharges.
- To differentiate this epilepsy subtype from typical BECCT.
Main Methods:
- Retrospective analysis of 7 pediatric patients (under 13 years) with sensorimotor seizures and no MRI abnormalities.
- Simultaneous electroencephalography and magnetoencephalography (MEG) were used to detect posteriorly oriented rolandic discharges.
Main Results:
- Patients experienced rolandic and atypical seizures (e.g., falling, head dropping, auditory hallucinations).
- Five patients had medically intractable seizures; two had well-controlled seizures with varying outcomes.
- Magnetoencephalography effectively detected posteriorly oriented rolandic discharges.
Conclusions:
- Posteriorly oriented rolandic discharges, detected by MEG, are indicative of an epilepsy type that excludes BECCT.
- This finding highlights a distinct epilepsy syndrome in children.
Background:
Benign childhood epilepsy with centro-temporal spikes (BECCT) is usually associated with anteriorly oriented rolandic discharges. We report an unusual type of childhood-onset epilepsy with sensorimotor seizures associated with posteriorly oriented rolandic discharges.
Methods:
Among 942 patients who underwent simultaneous electroencephalography and magnetoencephalography (MEG) for epilepsy evaluation, we found 7 patients with sensorimotor seizures aged under 13 years at onset, with no abnormal magnetic resonance imaging findings, and posteriorly oriented rolandic discharges detected by MEG. Ictal and interictal symptoms were evaluated retrospectively.
Result:
All patients had rolandic seizures as well as atypical seizures, such as falling, head dropping, auditory hallucinations, postural symptoms and/or automatism. Seizures were medically intractable in 5 patients and well controlled in 2, one of whom had behavioral problems and the other had transient graphomotor impairment.
Conclusion:
Posteriorly oriented rolandic discharges are better detected by MEG, and would exclude BECCT.
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