Abstract
Background: Continuous spike wave in sleep (CSWS) is an electroencephalogram (EEG) pattern associated with developmental and epileptic encephalopathy with spike-and-wave activation in sleep (DEE-SWAS). This etiologically heterogeneous syndrome may occur because of genetic factors and congenital or acquired brain lesions. We studied the pattern of clinical presentation and underlying etiologies in patients with DEE-SWAS that respond to resective surgery. Methods: We reviewed our clinical and research databases for patients who had resolution of CSWS following surgical resection of a focal lesion. Results: We identified 5 patients meeting inclusion criteria. In 3 of 5, an epileptogenic structural abnormality was not apparent on brain magnetic resonance imaging (MRI). In all 3 patients, focal cortical dysplasia was identified through intracranial EEG monitoring. Significance: DEE-SWAS may be a secondary bilateral network epilepsy syndrome, which can be treated with resection of the inciting focal lesion. In patients with drug-resistant CSWS, clinicians should consider a complete epilepsy presurgical workup, including intracranial EEG monitoring.
| Original language | English |
|---|---|
| Pages (from-to) | 992-1002 |
| Number of pages | 11 |
| Journal | Journal of Child Neurology |
| Volume | 37 |
| Issue number | 12-14 |
| DOIs | |
| State | Published - Dec 2022 |
Keywords
- continuous spike wave in sleep
- electrical status epilepticus in sleep
- epilepsy surgery
- focal cortical dysplasia
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