Cui Cathy K, Wong Wui-Kwan, Wong Chong H, Gill Deepak, Fong Michael W K
Westmead Comprehensive Epilepsy Centre, The University of Sydney, Sydney, NSW, Australia.
T. Y. Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, Sydney, NSW, Australia.
Front Netw Physiol. 2024 Jul 11;4:1425329. doi: 10.3389/fnetp.2024.1425329. eCollection 2024.
We present two cases with focal seizures where scalp electroencephalography (EEG) had prominent features of a developmental and epileptic encephalopathy (DEE): Case 1: a 17-year-old male with complex motor seizures whose EEG demonstrated a slow spike-and-wave pattern and generalized paroxysmal fast activity (GPFA). Case 2: a 12-year-old male with startle-induced asymmetric tonic seizures whose EEG also had a slow spike-and-wave pattern. Both patients had intracranial EEG assessment, and focal cortical resections resulted in long-term seizure freedom and resolution of generalized findings. These cases exemplify patients with focal epilepsy with networks that share similarities to generalized epilepsies, and importantly, these features did not preclude curative epilepsy surgery.
我们报告了两例局灶性癫痫发作的病例,其头皮脑电图(EEG)具有发育性和癫痫性脑病(DEE)的显著特征:病例1:一名17岁男性,有复杂运动性癫痫发作,其EEG显示慢棘波-慢波模式和广泛性阵发性快活动(GPFA)。病例2:一名12岁男性,有惊吓诱发的不对称强直性癫痫发作,其EEG也有慢棘波-慢波模式。两名患者均进行了颅内EEG评估,局灶性皮质切除术使癫痫长期缓解,并消除了广泛性异常。这些病例表明,局灶性癫痫患者的神经网络与全身性癫痫有相似之处,重要的是,这些特征并不排除进行根治性癫痫手术。