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Disconnective hemispherectomy for hemispheric dysplasia
Jean Guy Villemure1, Kathleen Meagher-Villemure, Jose Luis Montes
1Neurosurgery Department, Lausanne University Hospital, Switzerland. jean-guy.villemure@chuv.hospvd.ch
Insights
Disconnective hemispherectomy significantly improved seizure control in children with extensive hemispheric brain dysplasia. This surgical approach offers a favorable outcome for intractable epilepsy, reducing complication rates.
Area of Science:
- Neurosurgery
- Pediatric Neurology
- Epileptology
Background:
- Intractable epilepsy in children often presents with diffuse hemispheric dysplastic pathology.
- Surgical intervention is considered for severe cases unresponsive to medical management.
Purpose of the Study:
- To evaluate the efficacy and safety of disconnective hemispherectomy for intractable epilepsy due to extensive hemispheric dysplasia.
- To assess seizure outcome and complication rates associated with these surgical techniques.
Main Methods:
- Retrospective analysis of 12 pediatric patients with intractable epilepsy and hemispheric dysplasia.
- Surgical treatment involved functional hemispherectomy or peri-insular hemispherotomy.
- Presurgical evaluation guided the selection of disconnective hemispherectomy.
Main Results:
- Over 70% of patients achieved Engel's seizure outcome class I post-surgery.
- An additional 18% experienced satisfactory seizure control.
- One case of unexplained death and one of early hydrocephalus were reported.
Conclusions:
- Disconnective hemispherectomy is a viable surgical option for improving seizure control in pediatric patients with extensive hemispheric dysplastic pathology.
- These disconnective techniques appear to lower complication rates compared to traditional hemispherectomy for this specific condition.
Abstract:
Twelve patients suffering from intractable epilepsy and presenting with radiological evidence of diffuse hemispheric involvement of a dysplastic process, were treated by disconnective hemispherectomy, either functional hemispherectomy or peri-insular hemispherotomy. The median age at surgery was 4.5 years old and the interval between seizure onset and surgery, 3 years. All patients underwent a presurgical evaluation that led to the suggestion of disconnective hemispherectomy. Over 70% of patients have remained in Engel's seizure outcome class I since surgery and another 18% have had a satisfactory seizure outcome. There was one unexplained death and one case of early hydrocephalus. Hemispherectomy offers the possibility to improve seizure control in the majority of patients undergoing surgery for extensive dysplastic pathology of the hemisphere. Disconnective techniques reduce the rate of complications in this specific pathology.
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