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Child Neurology: Neurophysiologic and Anatomical Correlates in Startle Epilepsy: A Comprehensive SEEG Investigation
Junhyung Kim1, Min-Jee Kim1, Mi-Sun Yum1
1From the Department of Neurological Surgery (J.K., S.H.H.), Asan Medical Center; and Department of Pediatrics (M.-J.K., M.-S.Y., T.-S.K.), Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, South Korea.
Abstract:
Startle epilepsy, characterized by startle-provoked epileptic seizures, was historically recognized as one of the reflex epilepsies but currently lacks classification as a specific epileptic syndrome because of insufficient characterization. This study presents an institutional experience and review of relevant literature focusing on the neurophysiologic and anatomical aspects of startle epilepsy. We describe a pediatric patient with an underlying structural etiology of left frontal encephalomalacia who continued to experience disabling seizures despite multiple antiseizure medications and previous palliative surgery. A comprehensive presurgical evaluation using SEEG led to the resection of the left supplementary motor area and adjacent middle cingulate cortex, resulting in successful seizure remission. A literature review on the surgical treatment of startle epilepsy revealed consistent reports of successful seizure remission through neocortical resection of the supplementary motor area and/or cingulate region. This case study and literature review highlights startle epilepsy as a distinct form of epilepsy with identifiable neurophysiologic and anatomical characteristics. Our observations emphasize the potential of resective surgery as a viable treatment option for startle epilepsy and underscore the importance of neurophysiologic monitoring in guiding surgical interventions.
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