AlQarni Abdullah Ali, AlQarni Ali Mohammed, Fatani Mohammed, Aldahmashi Ali Mekbel, Alfaifi Jaber A
Department of Medicine, College of Medicine, University of Bisha, P.O. Box 61922, Bisha, Saudi Arabia.
Department of Radiology, Prince Mshiari Bin Saud Hospital, Al-Baha, Saudi Arabia.
Ann Med Surg (Lond). 2022 Jul 31;80:104257. doi: 10.1016/j.amsu.2022.104257. eCollection 2022 Aug.
and importance: An uncommon condition is congenital unilateral agenesis of the internal carotid artery (ICA). Most instances are asymptomatic due to adequate collateral circulation via the circle of Willis, but individuals might potentially manifest (or show) ischemic or aneurysmal dilatation hemorrhagic cerebrovascular lesions. The bony carotid canal must be absent from distinguishing this abnormality from chronic ICA blockage. Neuroradiologists must be aware of this condition since these patients have a higher risk of developing numerous intracranial diseases.
This report focuses on the case of 39 years male with an absent right internal carotid artery with posterior cerebral artery aneurism whose main symptoms were on and off headaches. In a discussion that includes demographic characteristics, clinical manifestations, radiologic findings, and an assessment of the risks associated with ICA agenesis.
Congenital agencies absence of carotid artery is rare variant anatomy although most of the time they are asymptomatic, it is known to increase the risk of aneurism and therefore, they need screening and close follow up.
及其重要性:先天性颈内动脉(ICA)单侧缺如是一种罕见病症。多数情况下,由于通过 Willis 环有足够的侧支循环,所以无症状,但个体可能会出现缺血性或动脉瘤样扩张性出血性脑血管病变。为将此异常与慢性颈内动脉阻塞相区分,骨性颈动脉管必须缺失。神经放射科医生必须了解这种情况,因为这些患者发生多种颅内疾病的风险更高。
本报告重点关注一名 39 岁男性,其右侧颈内动脉缺如并伴有大脑后动脉动脉瘤,主要症状为间歇性头痛。讨论内容包括人口统计学特征、临床表现、影像学检查结果以及对与颈内动脉缺如相关风险的评估。
先天性颈动脉缺如是一种罕见的解剖变异,尽管大多数时候无症状,但已知其会增加动脉瘤风险,因此,需要进行筛查并密切随访。