Arráez-Aybar L A, Villar-Martin A, Poyatos-Ruiperez C, Rodriguez-Boto G, Arrazola-Garcia J
Department of Anatomy and Embryology 2, Faculty of Medicine, University Complutense, 28040 Madrid, Spain.
Surg Radiol Anat. 2013 Aug;35(6):487-93. doi: 10.1007/s00276-012-1053-5. Epub 2012 Dec 19.
Fenestration of the basilar artery (BA) is a rare anatomical variation in comparison to those of the other intracranial arteries constituting the cerebral arterial circle. The incidence is difficult to ascertain and data vary according to type of series and modalities of detection. Basilar artery fenestration (BAF) has been reported in association with arteriovenous malformations, vascular variants, other developmental anomalies and neurovascular conflicts as a consequence of relations between the arterial branches of the BA and the nerves and other structures in the posterior cranial fossa. However, the real clinical interest of BAF is due to the possible formation of an aneurysm at the junction of the fenestrated segment and less frequently to the thrombosis of the vessels. With the aim to establish the prevalence of BAF in our population, we made a transversal pilot study of the first 200 MR angiographies performed on patients attending for the first time to control their base pathology (vascular or not). We have described three patients with this condition (representing a prevalence of 1.5 % on MR angiography) to shed additional light on this anomaly, two cases located at 1/3 proximal end (type 1-BAF) and one case located at joint 1/3 medium-1/3 distal end, locating distal to the anterior inferior cerebellar artery (type 4-BAF). In neither case was any other lesion found (i.e. aneurysm, infarctions, ischemia or thromboembolism). The pertinent clinical anatomy and embryological basis for this variation are reviewed, and the possible clinical implications and associated findings are discussed.
与构成脑动脉环的其他颅内动脉相比,基底动脉开窗是一种罕见的解剖变异。其发病率难以确定,数据因系列类型和检测方式而异。据报道,基底动脉开窗(BAF)与动静脉畸形、血管变异、其他发育异常以及神经血管冲突有关,这是由于基底动脉分支与后颅窝神经及其他结构之间的关系所致。然而,BAF真正的临床意义在于在开窗段交界处可能形成动脉瘤,较少情况下是血管血栓形成。为了确定BAF在我们人群中的患病率,我们对首次前来控制基础疾病(是否为血管性疾病)的患者进行的前200例磁共振血管造影进行了横断面试点研究。我们描述了3例患有这种情况的患者(在磁共振血管造影中的患病率为1.5%),以进一步阐明这种异常情况,2例位于近端1/3处(1型BAF),1例位于中1/3与远1/3交界处,位于小脑前下动脉远端(4型BAF)。在任何病例中均未发现其他病变(即动脉瘤、梗死、缺血或血栓栓塞)。本文回顾了这种变异相关的临床解剖学和胚胎学基础,并讨论了可能的临床意义及相关发现。