Department of Neurology, Chongqing City Hospital of Traditional Chinese Medicine, No. 6, Seventh Branch Road, Panxi, Jiangbei District, Chong qing, 400021, China.
BMC Neurol. 2020 Jun 23;20(1):253. doi: 10.1186/s12883-020-01832-y.
Aortic dissection (AoD) is a disease with a high mortality rate. Its clinical manifestations are diverse and covert, which makes diagnosis and treatment challenging. Here, we report a very rare case of aortic dissection leading to bilateral cerebral cortex ischaemia and epilepsy.
A 54-year-old man was admitted to the hospital with acute onset of right limb weakness accompanied by slurred speech. He had a history of hypertension as well as tobacco and alcohol use. The patient was found to have aphasia and right hemiplegia on physical examination. No bleeding was seen on the skull CT. Acute cerebral infarction was considered after admission, and rt-PA was administered for intravenous thrombolysis. During intravenous thrombolysis, the patient suddenly developed epilepsy, and diazepam was given immediately by intravenous injection to control the symptoms. Emergency skull diffusion-weighted imaging (DWI) was performed, and the results showed a small, patchy, high signal that was scattered throughout the left brain hemisphere, right frontal parietal lobe and centrum semiovale. Head and neck CT angiography (CTA) was performed; dissection was found in the ascending aorta, aortic arch, bilateral common carotid artery, proximal part of the internal carotid artery, and initial segment of the left external carotid artery. The laceration was located in the upper part of the ascending aorta. AoD complicated by acute cerebral infarction and epilepsy was considered, and the patient was immediately transferred to the cardiovascular surgery specialist hospital for surgical treatment.
Some aortic dissections have no typical manifestations of chest pain, and the onset is covert. Atypical clinical manifestations of epilepsy secondary to bilateral cerebral hemisphere infarction may appear. AoD with cerebral infarction is a contraindication for intravenous thrombolysis; surgical treatment is the best way to reduce mortality.
主动脉夹层(AoD)是一种死亡率较高的疾病。其临床表现多样且隐匿,这使得诊断和治疗具有挑战性。在这里,我们报告了一例非常罕见的主动脉夹层导致双侧大脑皮层缺血和癫痫的病例。
一名 54 岁男性因右侧肢体无力伴言语不清急性入院。他有高血压病史以及吸烟和饮酒史。体格检查发现患者存在失语症和右侧偏瘫。头颅 CT 未见出血。入院后考虑急性脑梗死,并给予 rt-PA 静脉溶栓治疗。在静脉溶栓过程中,患者突然出现癫痫发作,立即静脉注射地西泮控制症状。紧急行头颅弥散加权成像(DWI),结果显示左大脑半球、右额顶叶和半卵圆中心散在的小片状、高信号。行头颈部 CT 血管造影(CTA),发现升主动脉、主动脉弓、双侧颈总动脉、颈内动脉近端和左颈外动脉起始部夹层。撕裂位于升主动脉上段。考虑 AoD 并发急性脑梗死和癫痫,立即转至心血管外科专科医院行手术治疗。
有些主动脉夹层没有典型的胸痛表现,起病隐匿。可能出现继发于双侧大脑半球梗死的不典型癫痫临床表现。脑梗死合并 AoD 是静脉溶栓的禁忌证;手术治疗是降低死亡率的最佳方法。