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应用多层螺旋 CT 血管造影术检测椎动脉基底动脉交界窗。

Fenestration of the vertebrobasilar junction detected with multidetector computed tomography angiography.

机构信息

Discipline of Clinical Anatomy, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Westville Campus, Durban, South Africa.

Department of Neurosurgery, School of Clinical Medicine, College of Health Sciences, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.

出版信息

Folia Morphol (Warsz). 2022;81(2):510-514. doi: 10.5603/FM.a2021.0028. Epub 2021 Mar 22.

Abstract

The complex embryonic origin of the vertebrobasilar system may result in a wide range of anatomical variations. It has been hypothesized that the formation of fenestrations are likely to occur due to the failure of regression of the bridging arteries that connect the longitudinal neural arteries during embryogenesis. Fenestration of the vertebrobasilar system is a rare anatomical variation that involves a luminal division of the artery, that has a single origin into two separate and parallel channels which are rejoined distally. Fenestrations are important anatomical variants in patients undergoing endovascular and invasive intracranial interventions. Vascular fenestration has been associated with aneurysms, arteriovenous malformations, neuralgia, and vertebrobasilar ischaemia. We report on 3 cases of fenestration at the vertebrobasilar junction in 1 female and 2 male patients, respectively, using multidetector computed tomography angiography. The length of the fenestrated segment of the artery measured 4.41 mm, 3.90 mm, and 5.90 mm, respectively in the patients. Our report is clinically important as the presence of this anatomical variation may influence the management of cervical and intracranial pathologies. Increased awareness of the prevalence of anatomic variations contributes to the advancement of noninvasive imaging capabilities.

摘要

椎基底动脉系统的胚胎起源复杂,可能导致解剖结构的广泛变异。据推测,由于胚胎发育过程中连接纵神经动脉的桥接动脉退化失败,导致出现孔裂。椎基底动脉系统的孔裂是一种罕见的解剖变异,涉及动脉管腔的分隔,其单一起源分为两个单独且平行的通道,在远端重新连接。孔裂是接受血管内和侵袭性颅内介入治疗的患者的重要解剖变异。血管孔裂与动脉瘤、动静脉畸形、神经痛和椎基底动脉缺血有关。我们报告了 3 例女性和 2 例男性患者在椎基底动脉交界处的孔裂,分别使用多层螺旋 CT 血管造影。患者的孔裂动脉节段长度分别为 4.41 毫米、3.90 毫米和 5.90 毫米。我们的报告具有重要的临床意义,因为这种解剖变异的存在可能会影响颈椎和颅内病变的治疗。提高对解剖变异普遍存在的认识有助于提高非侵入性成像能力。

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