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Updated: May 19, 2026

Anteromesial Temporal Lobectomy for Medically Intractable Temporal Lobe Epilepsy: An Operative Study
Published on: August 15, 2025
Late-onset epileptic spasms may be cured by focal cortical resective surgery
Brigitte Ricard-Mousnier1, Georg Dorfmuller, Martine Fohlen
1Centre Hospitalier Universitaire, Neurology Department, Angers, Centre Hospitalier Universitaire, Pediatric Department, Angers.
Insights
This case study highlights successful surgical treatment for late-onset epileptic spasms in a child. Focal frontal cortectomy significantly reduced spasms, demonstrating the efficacy of targeted resection even with unclear EEG findings.
Area of Science:
- Pediatric Neurology
- Epileptology
- Neurosurgery
Background:
- Epileptic spasms, particularly late-onset and isolated forms, can present diagnostic challenges.
- Pharmacoresistant seizures necessitate exploration of alternative treatment strategies.
- Identifying the precise seizure onset zone is crucial for effective surgical intervention.
Purpose of the Study:
- To report a case of isolated late-onset epileptic spasms successfully treated with focal frontal cortectomy.
- To illustrate the utility of advanced neuroimaging and electrophysiological techniques in localizing seizure origins.
- To demonstrate that surgical resection can be curative even without clear surface EEG localization.
Main Methods:
- Case report detailing a child with late-onset epileptic spasms.
- Utilized interictal and ictal video-EEG, MRI, FDG-PET, and PET-MRI co-recording.
- Performed SEEG (Stereoelectroencephalography) for detailed ictal discharge mapping.
- Conducted a tailored focal frontal resection.
Main Results:
- The child presented with pharmacoresistant, sleep-only epileptic spasms starting at age 2.
- MRI revealed a white matter abnormality in the left frontal superior gyrus.
- FDG-PET and PET-MRI confirmed localized cortical hypometabolism.
- SEEG identified localized discharge correlating with the MRI lesion.
- Post-focal frontal cortectomy, spasms significantly reduced (Engel class II).
Conclusions:
- Isolated late-onset epileptic spasms can be effectively treated with focal cortical resection.
- Advanced imaging (MRI, PET) and SEEG are vital for localizing seizure foci when surface EEG is inconclusive.
- Surgical intervention can lead to significant seizure reduction and improved outcomes in select cases.
Abstract:
We report the case of a child with isolated late-onset epileptic spasms who significantly improved after focal frontal cortectomy. Clusters of axial and limb tonic contractions with head nodding began at 2 years of age. They occurred only during sleep, lasting 15 to 20 minutes and were pharmacoresistant. The child suffered slight mental delay. Interictal EEG showed left frontal spikes in slow sleep. Ictal video-EEG showed patterns of asymmetric spasms. MRI revealed a distinct white matter abnormality in the left frontal superior gyrus, corresponding clearly to localised cortical hypometabolism on FDG-PET and PET-MRI co-recording. SEEG investigation showed that the first spasm of the clusters corresponded to a localised discharge of rapid rhythms from the electrodes placed within the area identified as a lesion by MRI. Discharges then became more diffuse across the left frontal and temporal electrodes throughout the duration of the cluster. A tailored focal frontal resection was performed at 16 years of age. Spasms were very rare during the following three years (Engel class II). This observation illustrates the fact that isolated epileptic spasms can be cured by focal cortical resection despite a lack of clearly localised EEG surface anomalies.
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