| Literature DB >> 26463919 |
Rui Zhang1, Wan Zhu1, Hua Su2.
Abstract
Brain arteriovenous malformation (bAVM) is an important cause of intracranial hemorrhage (ICH), particularly in the young population. ICH is the first clinical symptom in about 50 % of bAVM patients. The vessels in bAVM are fragile and prone to rupture, causing bleeding into the brain. About 30 % of unruptured and non-hemorrhagic bAVMs demonstrate microscopic evidence of hemosiderin in the vascular wall. In bAVM mouse models, vascular mural cell coverage is reduced in the AVM lesion, accompanied by vascular leakage and microhemorrhage. In this review, we discuss possible signaling pathways involved in abnormal vascular development in bAVM.Entities:
Keywords: Brain arteriovenous malformations; Delta-like ligand-4; Microhemorrhage; Mural cell coverage; Notch; Platelet-derived growth factor receptor beta; Vascular integrity; Vascular leakage
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Year: 2016 PMID: 26463919 PMCID: PMC4654926 DOI: 10.1007/978-3-319-18497-5_6
Source DB: PubMed Journal: Acta Neurochir Suppl ISSN: 0065-1419