Serviço de Angiologia e Cirurgia Vascular, Centro Hospitalar de Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Portugal; Unidade de Angiologia e Cirurgia Vascular da Faculdade de Medicina da Universidade do Porto, Porto, Portugal.
Port J Card Thorac Vasc Surg. 2022 Apr 11;29(1):75-79. doi: 10.48729/pjctvs.148.
A right aortic arch and agenesis of internal carotid artery (ICA) are both extremely rare vascular devel- opment anomalies. Etiology of the both anomalies might be associated with the abnormal regression of the dorsal aorta. Most cases of ICA are asymptomatic due to sufficient collateral circulation and it is usually an incident finding on head and neck imaging by color Doppler ultrasonography, computed tomography (CT) or magnetic resonance imaging (MRI). ICA agenesis has a significant association - 24-67% - with intracranial aneurysms and their early detection can spare the patient serious complications.
A 28-year-old male had a single episode of hypertension that motivated the realization of several tests. During the investigation he was submitted to a duplex ultrasonography that revealed a diffuse narrowing of the left common carotid artery (CCA), with a markedly decrease in the peak systolic velocity and the absence of the left internal carotid artery (ICA) was suspected. Contrast-enhanced computed tomography (CT) demonstrated no abnormalities, such as cerebral infarc- tion or intracranial vascular malformations, but confirmed a right-sided aortic-arch, with anomalous origin of the left subcla- vian artery with a common origin of both CCAs and the absence of the left ICA. Examination of the head CT in bone window demonstrated an absence of the left internal carotid canal.
This clinical case emphasizes the importance of recognizing this condition due to the associated hemody- namic changes and in order to discover and evaluate other additional vascular malformations (aneurysms, collateral channels) and their life threatening potential risks (subarachnoid hemorrhage or ischemia). Also, it has a special importance in case of planning carotid or trans-sphenoidal hypophyseal surgery. To our knowledge, only 8 cases have been reported right aortic arch associated with agenesis of the left internal carotid artery.
右位主动脉弓和颈内动脉(ICA)发育不全均为极其罕见的血管发育异常。这两种异常的病因可能与背主动脉的异常退化有关。由于存在充分的侧支循环,大多数 ICA 病例无症状,在通过彩色多普勒超声、计算机断层扫描(CT)或磁共振成像(MRI)进行头颈部成像时通常是偶然发现的。ICA 发育不全与颅内动脉瘤有显著关联 - 24-67% - ,早期发现可使患者免于严重并发症。
一名 28 岁男性曾出现过一次高血压发作,这促使他进行了多项检查。在检查过程中,他接受了双功超声检查,发现左侧颈总动脉(CCA)弥漫性狭窄,收缩期峰值速度明显下降,疑似左侧颈内动脉(ICA)缺失。增强 CT 检查未发现脑梗死或颅内血管畸形等异常,但证实了右侧主动脉弓,左侧锁骨下动脉起源异常,两侧 CCA 共干,左侧 ICA 缺失。头部 CT 骨窗检查显示左侧颈内动脉管缺失。
该临床病例强调了认识这种情况的重要性,因为它会引起血流动力学变化,并且有助于发现和评估其他额外的血管畸形(动脉瘤、侧支通道)及其潜在的危及生命的风险(蛛网膜下腔出血或缺血)。此外,在计划颈动脉或经蝶垂体手术时,这种情况具有特殊的重要性。据我们所知,仅有 8 例报告了右位主动脉弓伴左侧颈内动脉发育不全。