国家神经系统疾病临床医学研究中心数据管理与共享系统

发表杂志：Neurological Sciences

发表类型: Article

影响因子(IF): 3.307

PMID: 29198042 Pubmed原文链接 全文下载

A 27-year-old man presented to the emergency department during Chinese spring festival with a history of seizures that had been occurring for the previous 5 days. The seizures were described by the paramedics as well as by bystanders as a Jacksonian seizure affecting the right limb, followed by a generalized tonic-clonic seizure lasting approximately 3 min. The patient had Todd’s paralysis of the right limb following each seizure. He did not exhibit any confusion between episodes and suffered approximately four seizures per day. The patient had previously been healthy. The family history was negative for seizures, endocrine disorders, or neoplasms. On physical examination, his vital signs were within normal limits, and he did not exhibit any focal neurological signs. Results of laboratory diagnostic tests performed on admission were within normal limits. Electroencephalogram (EEG) was performed at another hospital and demonstrated a few amount of spikes in the left temporal and frontal regions. Brain magnetic resonance imaging (MRI) without enhancement was performed at the same hospital as the EEG and did not reveal any abnormalities. A thoracic Xray showed normal results. Following these initial tests, the patient was diagnosed as epilepsy without known cause.