Gelastic epilepsy: Beyond hypothalamic hamartomas

• Main Authors: Reinaldo Uribe-San-Martin, Ethel Ciampi, Balduin Lawson-Peralta, Keryma Acevedo-Gallinato, Gonzalo Torrealba-Marchant, Manuel Campos-Puebla, Jaime Godoy-Fernández
• Format: Article
• Language: English
• Published: Elsevier 2015-01-01
• Series: Epilepsy and Behavior Case Reports
• Subjects: Gelastic epilepsy; Gelastic seizures; Epilepsy surgery; Neurocysticercosis
• Online Access: http://www.sciencedirect.com/science/article/pii/S2213323215000304

Gelastic epilepsy or laughing seizures have been historically related to children with hypothalamic hamartomas. We report three adult patients who had gelastic epilepsy, defined as the presence of seizures with a prominent laugh component, including brain imaging, surface/invasive electroencephalography, positron emission tomography, and medical/surgical outcomes. None of the patients had hamartoma or other hypothalamic lesion. Two patients were classified as having refractory epilepsy (one had biopsy-proven neurocysticercosis and the other one hippocampal sclerosis and temporal cortical dysplasia). The third patient had no lesion on MRI and had complete control with carbamazepine. Both lesional patients underwent resective surgery, one with complete seizure control and the other one with poor outcome. Although hypothalamic hamartomas should always be ruled out in patients with gelastic epilepsy, laughing seizures can also arise from frontal and temporal lobe foci, which can be surgically removed. In addition, we present the first case of gelastic epilepsy due to neurocysticercosis.