Pascual-Castroviejo Ignacio, Alvarez-Linera Juan, Coya Juan, Viaño Juan, Pascual-Pascual Samuel-Ignacio, Velázquez-Fragua Ramón, López-Gutiérrez Juan-Carlos
Pediatric Neurology Service, University Hospital La Paz, Madrid, Spain.
Childs Nerv Syst. 2011 Apr;27(4):617-25. doi: 10.1007/s00381-010-1242-7. Epub 2010 Jul 31.
Cutaneous hemangioma and vascular malformation are two vascular abnormalities frequently associated with absence or hypoplasia of one or both carotid and/or vertebral arteries, presence of persistent embryonic arteries, especially the trigeminal, cerebellar malformations, and coarctation of the aortic arch and/or congenital cardiopathy. This disease is known as Pascual-Castroviejo type II syndrome (P-CIIS) and by the acronym PHACE.
Three patients (two females and one male) with facial hemangioma are studied during the first years of age by magnetic resonance angiography (MRA) and their vascular evolution to adult age followed through several MRA controls.
All the three patients showed persistence of the trigeminal artery associated to other intra- and extracranial vascular abnormalities of type hemangioma or hemangiomatous arteries that presented progressive involution with decreased arterial caliber without appearing cerebrovascular stroke or hypoxic zones because, at the same time, collateral vascularization appeared through connections between the embryonic arteries and the peripheral branches of the internal carotids or connections between branches of the external and internal carotids. Only one patient had obstruction of a branch of the left middle cerebral artery after 3 days, with gastroenteritis with elevated fever at 17 months of life that caused parenchymal infarct in the left cerebral region supplied by the obstructed artery.
The presence of embryonic arteries, especially the trigeminal, and connections between branches of the internal and external carotids, mainly through the internal maxillary and ophthalmic arteries, ensure the cerebral supply in the P-CIIS despite the progressive involvement of the cerebral arteries.
皮肤血管瘤和血管畸形是两种血管异常疾病,常与一侧或双侧颈动脉和/或椎动脉缺如或发育不全、持续性胚胎动脉(尤其是三叉动脉)存在、小脑畸形以及主动脉弓缩窄和/或先天性心脏病相关。这种疾病被称为帕斯夸尔 - 卡斯特罗维霍II型综合征(P - CIIS),简称为PHACE。
对三名面部血管瘤患者(两名女性和一名男性)在其幼年时进行磁共振血管造影(MRA)研究,并通过多次MRA检查跟踪其血管发育至成年期。
所有三名患者均显示三叉动脉持续存在,并伴有其他血管瘤或血管瘤样动脉的颅内和颅外血管异常,这些异常呈现出渐进性消退,动脉管径减小,未出现脑血管中风或缺氧区域,因为与此同时,通过胚胎动脉与颈内动脉外周分支之间的连接或颈外动脉与颈内动脉分支之间的连接出现了侧支血管形成。只有一名患者在3天后出现左大脑中动脉一支的阻塞,该患者在17个月大时因肠胃炎伴高热导致由阻塞动脉供血的左脑区域实质梗死。
尽管脑动脉逐渐受累,但胚胎动脉(尤其是三叉动脉)的存在以及颈内动脉和颈外动脉分支之间的连接(主要通过上颌内动脉和眼动脉)确保了P - CIIS患者的脑供血。