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新发脑动静脉畸形及其形成理论综述

De novo intracerebral arteriovenous malformations and a review of the theories of their formation.

作者信息

Dalton A, Dobson G, Prasad M, Mukerji N

机构信息

a James Cook University Hospital , Middlesbrough , UK.

出版信息

Br J Neurosurg. 2018 Jun;32(3):305-311. doi: 10.1080/02688697.2018.1478060. Epub 2018 Jun 6.

Abstract

PURPOSE

Arteriovenous malformations (AVM) are still frequently described as congenital lesions in medical texts despite little evidence existing for their congenital nature. Increasing numbers of case reports of de novo AVMs add weight to the notion that they are dynamic lesions and that they can form postnatally. A thorough review of all reported cases of de novo AVM formation and a review of articles relating to AVM pathogenesis was planned to summarise current research on AVM pathogenesis and provide insight into the future implications for AVM research and treatment.

METHODS AND RESULTS

MEDLINE was searched to find 29 cases of de novo AVM formation with prior MRI imaging, nine of which also had prior digital subtraction angiography. A discussion of AVM pathogenesis is undertaken through a review of articles relating to AVM embryology, postnatal angiogenesis, syndromic forms of AVMs and studies of AVM molecular biology and genetics in human and animal models.

CONCLUSIONS

There is little evidence for an embryological origin through dysregulated vasculogenesis, whereas there is a raft of evidence to support dysregulated angiogenesis in childhood or even adulthood. Translational implications include risk stratification by biomarkers for predicting haemorrhage and novel therapeutic approaches to suppress AVM proliferation and initiate reversal.

摘要

目的

尽管几乎没有证据表明动静脉畸形(AVM)具有先天性,但在医学文献中它们仍经常被描述为先天性病变。越来越多关于新发AVM的病例报告支持了这样一种观点,即它们是动态病变,可在出生后形成。计划对所有已报告的新发AVM形成病例进行全面回顾,并对与AVM发病机制相关的文章进行综述,以总结当前关于AVM发病机制的研究,并深入了解AVM研究和治疗的未来意义。

方法与结果

检索MEDLINE以查找29例有先前MRI成像的新发AVM形成病例,其中9例还进行了先前的数字减影血管造影。通过回顾与AVM胚胎学、出生后血管生成、AVM综合征形式以及人类和动物模型中AVM分子生物学和遗传学研究相关的文章,对AVM发病机制进行了讨论。

结论

几乎没有证据表明AVM起源于胚胎期血管生成失调,而有大量证据支持儿童期甚至成年期血管生成失调。转化意义包括通过生物标志物进行风险分层以预测出血,以及采用新的治疗方法来抑制AVM增殖并启动逆转。

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