Lee Jung-Ju, Park Jong-Moo, Kang Kyusik, Kwon Ohyun, Lee Woong-Woo, Kim Byung-Kun
Department of Neurology, Nowon Eulji Medical Center, Eulji University, Seoul, Korea.
Department of Neurology, Uijeongbu Eulji Medical Center, Eulji University, Kyeongkido, Korea.
Clin Med Insights Case Rep. 2021 Apr 10;14:11795476211009241. doi: 10.1177/11795476211009241. eCollection 2021.
Aphasic status epilepticus (ASE) is unusual and has clinical characteristics similar to those of other disorders. Herein, we report 3 cases of ASE. A left-handed man (patient 1) showed continuous aphasia after the administration of flumazenil. He had underlying alcoholic liver cirrhosis and traumatic brain lesions in the right hemisphere. Electroencephalography (EEG) revealed periodic epileptiform discharges in the right frontotemporal area, which were intervened by rhythmic activity with spatiotemporal evolutions. A right-handed woman (patient 2) showed recurrent aphasia. Blood tests revealed a high blood glucose level (546 mg/dL) and high serum osmolality (309 mMol/L). Her EEG showed rhythmic activity in the left frontotemporal area with spatiotemporal evolutions on a normal background rhythm. She became seizure-free after the administration of an antiepileptic drug and strict glucose regulation. A right-handed woman (patient 3) developed subacute aphasia a week before hospital admission. She had a gradual decline of cognition 1 year before. Her EEG showed intermittent quasi-rhythmic fast activity in the frontotemporal area bilaterally, with fluctuating frequency and amplitude. The patient became seizure-free after the administration of an antiepileptic drug. Brain single-photon emission tomography performed after seizure control showed decreased perfusion in the left frontotemporal area. After discharge, her cognitive function gradually declined to a severe state of dementia. ASE can be caused by diverse etiologies; it is usually caused by cerebral lesions and less frequently by non-lesional etiologies or degenerative disorders. Adequate treatment of underlying disorders and seizures is critical for curing the symptoms of ASE.
失语性癫痫持续状态(ASE)较为罕见,具有与其他疾病相似的临床特征。在此,我们报告3例ASE病例。一名左利手男性(患者1)在使用氟马西尼后出现持续性失语。他患有潜在的酒精性肝硬化和右侧半球脑外伤。脑电图(EEG)显示右侧额颞区有周期性癫痫样放电,并伴有具有时空演变的节律性活动。一名右利手女性(患者2)出现反复失语。血液检查显示血糖水平高(546mg/dL)和血清渗透压高(309mMol/L)。她的脑电图显示左侧额颞区在正常背景节律上有具有时空演变的节律性活动。在使用抗癫痫药物并严格控制血糖后,她不再发作。一名右利手女性(患者3)在入院前一周出现亚急性失语。她在1年前认知功能逐渐下降。她的脑电图显示双侧额颞区间歇性准节律性快活动,频率和幅度波动。在使用抗癫痫药物后,该患者不再发作。癫痫控制后进行的脑单光子发射断层扫描显示左侧额颞区灌注减少。出院后,她的认知功能逐渐下降至严重痴呆状态。ASE可由多种病因引起;通常由脑部病变引起,较少由非病变性病因或退行性疾病引起。充分治疗潜在疾病和癫痫发作对于治愈ASE症状至关重要。