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毛细血管性胎记在非外伤性脑出血患儿中作为毛细血管畸形-动静脉畸形综合征的重要标志物的潜力。

The potential of capillary birthmarks as a significant marker for capillary malformation-arteriovenous malformation syndrome in children who had nontraumatic cerebral hemorrhage.

机构信息

Douglas Stephens Surgical Research Unit, Murdoch Children's Research Institute, Melbourne, Australia.

出版信息

J Pediatr Surg. 2010 Dec;45(12):2419-22. doi: 10.1016/j.jpedsurg.2010.08.043.

DOI:10.1016/j.jpedsurg.2010.08.043
PMID:21129558
Abstract

BACKGROUND/PURPOSE: Capillary malformation-arteriovenous malformation (CM-AVM) is a new autosomal dominant disorder with cutaneous capillary malformations (CM) and high-flow cerebral arteriovenous malformations (AVM). Patients may have Parkes-Weber syndrome. This study determined if cutaneous CM are a significant indicator of CM-AVM in children with cerebral bleeds.

METHODS

Children with cerebral AVMs between 1991 and 2009 were reviewed. A family history of brain hemorrhage, AVMs, or cutaneous birthmarks was elicited. Patients and siblings were examined for CM and a family tree recorded. A brief questionnaire determined the family's opinion regarding screening for this syndrome.

RESULTS

Of 30 families, 1 family had Parkes-Weber syndrome. In 3 families, both patient and relatives had CM. In 9 families, patients had no CM, but relatives had them. One family had hereditary hemorrhagic telangiectasia. From the survey, 80% of families would be concerned about vascular marks, and 87% of families would allow screening for cerebral AVMs.

CONCLUSION

A family history of vascular marks may predict families at risk of having a cerebral AVM with hemorrhage. Most families would agree to screening. However, family history and physical examination alone do not confirm CM-AVM but form a useful screening tool to identify families needing further investigations with genetic testing and/or magnetic resonance imaging.

摘要

背景/目的:毛细血管畸形-动静脉畸形(CM-AVM)是一种新的常染色体显性遗传疾病,伴有皮肤毛细血管畸形(CM)和高流量脑动静脉畸形(AVM)。患者可能患有 Parkes-Weber 综合征。本研究旨在确定在发生脑溢血的儿童中,皮肤 CM 是否是 CM-AVM 的重要指标。

方法

回顾了 1991 年至 2009 年间患有脑动静脉畸形的儿童。询问了家族中是否有脑出血、AVM 或皮肤出生缺陷的病史。检查患者和兄弟姐妹是否存在 CM,并记录家族树。通过简短的问卷调查确定了该家庭对该综合征筛查的看法。

结果

在 30 个家庭中,有 1 个家庭患有 Parkes-Weber 综合征。在 3 个家庭中,患者和亲属均存在 CM。在 9 个家庭中,患者没有 CM,但亲属有。1 个家庭患有遗传性出血性毛细血管扩张症。根据调查,80%的家庭会关注血管标记,87%的家庭会允许筛查脑 AVM。

结论

家族史中有血管标记可能预示着有发生脑出血的脑 AVM 的风险。大多数家庭会同意筛查。然而,仅凭家族史和体格检查并不能确诊 CM-AVM,但可以作为有用的筛查工具,以确定需要进一步进行基因检测和/或磁共振成像检查的家庭。

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