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三叉动脉的解剖学方面。

Trigeminal artery anatomical aspects.

作者信息

Bulbuc Ionuț, Iliescu Dan Marcel, Dina Constantin, Ionescu Constantin, Bordei Petru

机构信息

Ovidius" University From Constanţa, Constanța, Romania.

出版信息

Surg Radiol Anat. 2025 Jan 4;47(1):54. doi: 10.1007/s00276-024-03553-0.

DOI:10.1007/s00276-024-03553-0
PMID:39754664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11700043/
Abstract

PURPOSE AND BACKGROUND

The trigeminal artery is a rare anatomical variant, representing an embryonic vestige of the anastomosis between the internal carotid artery and the posterior circulator system, that can be asymptomatic or could have vast clinical manifestations produced by insufficient flow or by vascular nervous conflicts. This study is an anatomical presentation of 3 trigeminal artery cases observed at Medimar Imagistic Services Constanta.

METHODS

The 3 trigeminal artery cases were discovered on a 860 magnetic resonance angiographies (0.35% of cases), made on a GE HD/e 8ch 1.5 T.

RESULTS

In all 3 cases, the arteries were rising from the right internal carotid artery and one from the left internal carotid artery, in 2 cases the origin was on the superior surface, and in one case, on the anterolateral surface, in all 3 cases from C4 horizontal cavernous segment. The artery caliber was between 2.7 mm and 5.1 mm; the artery length was between 26 and 32 mm. Other associated vascular malformations were: partial or total basilar artery hypoplasia, in one case posterior communicant artery agenesis, contralateral vertebral artery hypoplasia, posterior cerebral artery hypoplasia (in 2 cases), and no anastomosis between the P1 segment of the posterior cerebral artery with the posterior communicating artery (one case).

CONCLUSIONS

While the trigeminal artery is a rare anatomical variant, it's still a very important vessel situated in the posterior cerebral fossa, which needs to be taken into account in the case of neurosurgical interventions.

摘要

目的与背景

三叉动脉是一种罕见的解剖变异,代表颈内动脉与后循环系统之间吻合的胚胎遗迹,可无症状,也可因血流不足或血管神经冲突而产生广泛的临床表现。本研究是对在康斯坦察Medimar影像服务中心观察到的3例三叉动脉病例的解剖学呈现。

方法

这3例三叉动脉病例是在GE HD/e 8通道1.5T磁共振血管造影检查的860例中发现的(占病例的0.35%)。

结果

在所有3例中,动脉均起自右侧颈内动脉,1例起自左侧颈内动脉;2例起源于上表面,1例起源于前外侧表面,所有3例均起自C4水平海绵窦段。动脉管径在2.7毫米至5.1毫米之间;动脉长度在26至32毫米之间。其他相关血管畸形包括:部分或完全基底动脉发育不全,1例后交通动脉缺如,对侧椎动脉发育不全,大脑后动脉发育不全(2例),大脑后动脉P1段与后交通动脉之间无吻合(1例)。

结论

虽然三叉动脉是一种罕见的解剖变异,但它仍是位于后颅窝的非常重要的血管,在神经外科手术中需要予以考虑。

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