Welman C J, Khangure M S
Department of Diagnostic and Interventional Radiology, Royal Perth Hospital, Perth, Western Australia, Australia.
Australas Radiol. 2007 Oct;51 Spec No.:B25-7. doi: 10.1111/j.1440-1673.2007.01697.x.
Bilateral internal carotid artery (ICA) agenesis is rare. A patient presented with symptoms of a transient ischaemic attack. Magnetic resonance imaging with magnetic resonance angiography showed multiple foci of chronic cerebral ischaemic change and bilaterally absent ICA. Cerebral supply was derived from the posterior circulation. Differentiation has to be made between congenital agenesis/hypoplasia and acquired ICA occlusion. Computed tomography through the skull base showed the absence of the carotid canals bilaterally confirming congenital ICA agenesis.
双侧颈内动脉发育不全较为罕见。一名患者出现短暂性脑缺血发作症状。磁共振成像及磁共振血管造影显示多处慢性脑缺血改变病灶,双侧颈内动脉缺如。脑部供血来自后循环。必须区分先天性发育不全/发育不良与后天性颈内动脉闭塞。经颅底计算机断层扫描显示双侧颈动脉管缺如,证实为先天性颈内动脉发育不全。