Rolandic epilepsy: an uncommon presentation with leg motor seizures
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Published on: September 20, 2024
Lucia Fusco1, Marina Trivisano, Nicola Specchio
1Division of Neurology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy. lucia.fusco@opbg.net
Insights
Rolandic epilepsy (RE), a common childhood epilepsy, can present with leg seizures. Recognizing this benign syndrome is crucial to avoid unnecessary investigations and treatments.
Area of Science:
- Pediatric Neurology
- Epileptology
Background:
- Rolandic epilepsy (RE) is the most common childhood epileptic syndrome, typically benign and self-limiting.
- Characterized by sleep-related orofacial seizures and specific EEG findings (centrotemporal spikes).
- Less common seizure presentations, like leg sensorimotor seizures, may be underestimated.
Purpose of the Study:
- To highlight the diagnostic challenge of Rolandic epilepsy when leg sensorimotor seizures are the predominant manifestation.
- To emphasize the importance of recognizing this benign syndrome to prevent unnecessary investigations and therapies.
Main Methods:
- Retrospective analysis of 230 children diagnosed with Rolandic epilepsy.
- Identification of cases where leg sensorimotor seizures were the primary ictal event.
Main Results:
- Six out of 230 (approximately 2.6%) children with RE presented primarily with leg sensorimotor seizures.
- These cases posed diagnostic difficulties, potentially leading to extensive workups and treatments.
Conclusions:
- Leg sensorimotor seizures can be an underrecognized presentation of Rolandic epilepsy.
- Early and accurate diagnosis of RE, even with atypical seizure types, is essential for appropriate management and avoiding overtreatment.
Abstract:
Rolandic epilepsy (RE) is the most common and one of the most benign epileptic syndromes of childhood. It is typically characterized by sleep-related orofacial seizures, of brief duration, of variable frequency, in otherwise healthy children. Electroencephalography (EEG) shows typical centrotemporal spike and spike-and-wave complexes, often bilateral and asynchronous, activated by sleep. Therapy is often unnecessary and seizures spontaneously end at puberty. Apart from typical orofacial localization, arm or more diffuse clonic jerks are frequently described by parents. More rare and probably underestimated are sensorimotor seizure localized to one leg. When such seizures represent the only type of seizures in RE, the exact recognition of this benign epileptic syndrome appears difficult, leading to unnecessary investigation and therapy. We describe six children, among 230 with RE, who presented leg sensorimotor seizures as the mainly type of ictal manifestations.
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