脑血管病双侧后交通动脉发育不全的尸检研究

A. Dumitrescu, A. Sava, D. Turliuc, A. Cucu, R. Șufaru, I. Gotcă, I. Grierosu, Ş. Turliuc
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引用次数: 1

摘要

目的:探讨双侧后交通动脉(PCoAs)发育不全的临床后果,为神经外科医生和神经科医生诊断和治疗脑卒中患者提供依据。材料和方法:我们对98个威利斯环(CW)的大体形态进行了解剖回顾性研究,这些环是在罗马尼亚东北部地区主要的神经和神经外科保健中心“教授博士N. Oblu”急诊临床医院(Iasi)对死亡患者进行尸检时确定的,为期三年。从病理科的登记和档案中获取了人口统计和尸检数据以及摄影图像。我们只研究了双侧PCoA发育不全且无其他相关解剖异常的CWs。结果:双侧pcoa发育不全5例(5.12%)。男女比例为3:2。平均年龄为63.5岁。80%的病例死于缺血性或出血性中风,但10%死于心脏病。在2例(40%)病例中,两个pcoa中的一个表现为发育不全,另一个表现为发育不全,这一事件与同侧额叶中风有关。在另外两个(40%)双动脉发育不全的病例中,死亡原因是位于脑干的缺血性中风。只有一例(20%),即使存在双侧pcoa发育不全,死亡原因也是非神经性的。结论:尽管文献认为PCoA发育不全仅在同侧颈内动脉(ICA)闭塞时才会成为缺血性卒中的危险因素,但在我们的研究中,我们发现与控制侧动脉发育不全相关的两种PCoA中的一种发育不全导致脑干缺血性卒中,从而揭示了PCoA在椎基底系统闭塞时保障后循环的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Autopsic Study on Bilateral Hypoplasiaof the Posterior Communicating Arteriesin Cerebrovascular Diseases
Objective: To identify the clinical consequences of bilateral hypoplasia of the posterior communicating arteries (PCoAs) in order to provide a clue to neurosurgeons and neurologists in their work to diagnose and treat patients with stroke symptoms. Material and methods: We performed an anatomical retrospective study on gross morphology of 98 circles of Willis (CW) that were identified at the time of the autopsies made on patients who have died in the "Prof. dr. N. Oblu” Emergency Clinical Hospital Iasi, Romania, the main neurological and neuro-surgical healthcare Centre in the region of North-Eastern Romania, for a period of three years. Demographical and autopsic data, as well as photographic images were taken from the registers and archives of the Pathology Department. Only CWs with bilateral hypoplasia of PCoA without any other associated anatomical abnormalities were studied. Results: In 5 cases (5.12%) we identified bilateral hypoplasia of PCoAs. Male: Female ratio was 3: 2. The average age was 63.5 years. 80% of cases died of ischemic or haemorrhagic stroke, but 10% died of heart disease. In 2 (40%) cases, one of the two PCoAs presented aplasia and the other was hypoplastic, an event related to frontal lobe strokes on the same side. In the other two (40%) cases in which both arteries were hypoplastic, the cause of death was ischemic stroke located in the brainstem. In only one case (20%), even in the presence of bilateral hypoplasia of PCoAs, the cause of death was non-neurological. Conclusion: Even if literature claims that PCoA hypoplasia becomes a risk factor for ischemic stroke only in the presence of ipsilateral internal carotid artery (ICA) occlusion, in our study we found that aplasia of one of the two PCoAs associated with hypoplasia of the controlateral artery caused ischemic stroke in the brainstem, thus revealing the role of PCoAs in ensuring the posterior circulation in case of occlusion of the vertebro-basilar system.
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