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Published on: December 18, 2016
The differences in epileptic characteristics in patients with porencephaly and schizencephaly
Miki Shimizu1, Tomoki Maeda, Tatsuro Izumi
1Department of Pediatrics and Child Neurology, Oita University Faculty of Medicine, Yufu, Oita, Japan. ntkymiki@oita-u.ac.jp
Insights
Epilepsy in porencephaly and schizencephaly differs, with porencephaly patients responding better to simpler treatments. Schizencephaly seizures are often intractable, suggesting complex lesion involvement.
Area of Science:
- Neurology
- Pediatric Neurology
- Epileptology
Background:
- Porencephaly and schizencephaly are rare brain malformations.
- Epileptic seizures are a common complication in these conditions.
- Understanding seizure characteristics is crucial for effective management.
Purpose of the Study:
- To compare epileptic characteristics in patients with porencephaly and schizencephaly.
- To evaluate the efficacy of different antiepileptic drug therapies.
Main Methods:
- Retrospective study of 11 patients with porencephaly and 8 with schizencephaly.
- Analysis of seizure types, onset, epilepsy syndromes, and EEG findings.
- Review of treatment responses to monotherapy, polytherapy, and specific drugs.
Main Results:
- Seizures were frequent in both extensive porencephaly and open-lip schizencephaly.
- West syndrome and early-onset seizures were observed in both groups.
- Porencephaly patients often achieved control with monotherapy (e.g., valproate), while schizencephaly seizures were frequently intractable despite polytherapy.
Conclusions:
- Epileptic intractability in schizencephaly may stem from widespread lesions and cortical dysplasia.
- Monotherapy or two-drug regimens are often more effective in porencephaly than extensive polytherapy.
- Treatment strategies should be tailored to the specific malformation and seizure characteristics.
Abstract:
The epileptic characteristics and their differences in patients with porencephaly and schizencephaly were, respectively, evaluated. Eleven patients with porencephaly and eight patients with schizencephaly were retrospectively enrolled in this study. Five of the six patients with extensive porencephaly and all five patients with open-lip schizencephaly had been suffering from various types of epileptic seizures. Three patients with extensive porencephaly and all five patients with open-lip schizencephaly had presented with early onset seizures before 9 months of age. Two patients with extensive porencephaly and three patients with open-lip schizencephaly had presented with West syndrome. These two groups of patients with epileptic seizures showed generalized epilepsy or generalized epilepsy with unilateral dominancy at the onset, and then developed localization-related epilepsy or unilateral seizures with increasing age. The epileptic paroxysms showed multifocal independent spikes, which were not always localized in the defect or cleft sites at the last examination. Polytherapy or synergistic combinations were eventually introduced for these intractable seizures in both groups for patients without any evidence of efficacy. In the porencephaly patients, four of five patients achieved good seizure control with appropriate monotherapy or two-drug therapy including valproate. All five patients with schizencephaly had been treated by polytherapy, and three of them had persistent intractable seizures in spite of trying rational monotherapy or two-drug therapy. The epileptic intractability associated with open-lip schizencephaly might be related to the epileptogenesis of these extensive and widespread defective lesions, which were commonly associated with cortical dysplasia. A trial of rational monotherapy or two-drug therapy may be effective, rather than larger-number polytherapy in many cases, more in porencephaly than schizencephaly.
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