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本文引用的文献

1
[Cutaneous hemangiomas and vascular malformations and associated pathology (Pascual-Castroviejo type II syndrome). Study of 41 patients].[皮肤血管瘤和血管畸形及相关病理学(帕斯夸尔 - 卡斯特罗维霍II型综合征)。41例患者的研究]
Rev Neurol. 2005;41(4):223-36.
2
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?面部血管瘤与皮质发育畸形:PHACE综合征谱系的扩展还是一种新的疾病实体?
Am J Med Genet A. 2004 Jan 15;124A(2):192-5. doi: 10.1002/ajmg.a.20316.
3
The biology of VEGF and its receptors.血管内皮生长因子(VEGF)及其受体的生物学特性
Nat Med. 2003 Jun;9(6):669-76. doi: 10.1038/nm0603-669.
4
Facial hemangioma and cerebral corticovascular dysplasia: a syndrome associated with epilepsy.
Neurology. 2003 Mar 25;60(6):1030-2. doi: 10.1212/01.wnl.0000052688.20517.7d.
5
PHACE syndrome: new views on diagnostic criteria.PHACE综合征:诊断标准的新观点
Eur J Pediatr Surg. 2002 Dec;12(6):366-74. doi: 10.1055/s-2002-36849.
6
The many faces of PHACE syndrome.PHACE综合征的多种表现
J Pediatr. 2001 Jul;139(1):117-23. doi: 10.1067/mpd.2001.114880.
7
Unilateral polymicrogyria: a common cause of hemiplegia of prenatal origin.单侧多小脑回畸形:产前偏瘫的常见病因。
Brain Dev. 2001 Jul;23(4):216-22. doi: 10.1016/s0387-7604(01)00211-x.
8
[Joint presentation of facial hemangioma, posterior fossa malformation, and carotid-vertebral hypoplasia (Pascual-Castroviejo syndrome II): report of 2 new cases].[面部血管瘤、后颅窝畸形和颈-椎发育不全联合表现(帕斯卡-卡斯特罗维霍综合征II型):2例新病例报告]
Rev Neurol. 2001;32(1):50-4.
9
The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain.头部神经嵴为面部和前脑的所有血管提供周细胞和平滑肌细胞。
Development. 2001 Apr;128(7):1059-68. doi: 10.1242/dev.128.7.1059.
10
Homeobox B3 promotes capillary morphogenesis and angiogenesis.同源盒B3促进毛细血管形态发生和血管生成。
J Cell Biol. 2000 Jan 24;148(2):343-51. doi: 10.1083/jcb.148.2.343.

面部血管瘤与半球迁移障碍:5例患者的病例报告

Facial hemangioma and hemispheric migration disorder: presentation of 5 patients.

作者信息

Pascual-Castroviejo I, Pascual-Pascual S-I, López-Gutiérrez J-C, Velazquez-Fragua R, Viaño J

机构信息

Pediatric Neurology Service, University Hospital La Paz, Madrid, Spain.

出版信息

AJNR Am J Neuroradiol. 2007 Sep;28(8):1609-12. doi: 10.3174/ajnr.A0583.

DOI:10.3174/ajnr.A0583
PMID:17846222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8134379/
Abstract

BACKGROUND AND PURPOSE

The association of cortical organization disorders with facial hemangiomas or vascular malformations has been described in only a few reports. The purpose of this study was to show the close association of these cutaneous anomalies with cortical dysplasias and intracranial vascular abnormalities.

MATERIALS AND METHODS

Five patients, all women, with cutaneous vascular abnormalities, 4 with hemangioma and 1 with vascular malformation, were studied with MR and MR angiography.

RESULTS

All 5 of the patients showed cortical dysplasia. The cutaneous lesions involved the left frontal region, ipsilateral to the cerebral hemisphere with cortical dysplasia, in all of the patients. Four patients had seizures that responded well to antiepileptic drugs. Hemispheric hypoplasia was associated with the cortical dysplasia in all 5 of the patients. Arterial abnormalities were found in all of the patients, consisting of aplasia of the ipsilateral internal carotid artery in 2, persistence of the trigeminal artery in 2, persistence of both proatlantal arteries and double kinking in the internal carotid artery in 1, and origin of both anterior cerebral arteries from the same internal carotid in all 5 of the patients, 1 of whom also showed an intracavernous anterior cerebral artery origin of the same side of the hemispheric hypoplasia and polymicrogyria. Seizures and mild psychomotor delay could be caused by the cortical dysplasia and the hemispheric hypoplasia.

CONCLUSIONS

The presence of many congenital vascular abnormalities in this series suggests that facial hemangioma and vascular malformations may be in close relationship with cortical and vascular abnormalities. The reason that the vascular and cortical abnormalities occurred in the left side in all 5 of the patients and the mechanism underlying the association of both malformations are unclear. A genetic origin is suggested.

摘要

背景与目的

仅有少数报告描述了皮质组织紊乱与面部血管瘤或血管畸形之间的关联。本研究的目的是表明这些皮肤异常与皮质发育异常和颅内血管异常密切相关。

材料与方法

对5例患有皮肤血管异常的女性患者进行了研究,其中4例为血管瘤,1例为血管畸形,均接受了磁共振成像(MR)和磁共振血管造影(MRA)检查。

结果

所有5例患者均表现出皮质发育异常。所有患者的皮肤病变均累及与存在皮质发育异常的大脑半球同侧的左额叶区域。4例患者有癫痫发作,对抗癫痫药物反应良好。所有5例患者的皮质发育异常均伴有半球发育不全。所有患者均发现动脉异常,其中2例同侧颈内动脉发育不全,2例三叉动脉持续存在,1例前寰椎动脉均持续存在且颈内动脉双折曲,所有5例患者双侧大脑前动脉均起自同一颈内动脉,其中1例还表现为半球发育不全和多小脑回同侧的海绵窦内大脑前动脉起源。癫痫发作和轻度精神运动发育迟缓可能由皮质发育异常和半球发育不全引起。

结论

本系列中存在多种先天性血管异常表明,面部血管瘤和血管畸形可能与皮质和血管异常密切相关。所有5例患者的血管和皮质异常均发生在左侧,以及两种畸形关联的潜在机制尚不清楚。提示可能存在遗传起源。