Intracranial pial arteriovenous fistula in infancy: a case report and literature review

被引：16
作者：
Kraneburg, U. M. [1 ]
Nga, V. D. W. [2 ]
Ting, E. Y. S. [3 ]
Hui, F. K. H. [4 ]
Lwin, S. [2 ]
Teo, C. [5 ]
Chou, N. [2 ]
Yeo, T. T. [2 ]
机构：
[1] Univ Witten Herdecke, Sch Med, Witten, Germany
[2] Natl Univ Singapore Hosp, Univ Surg Cluster, Div Neurosurg, Singapore 119074, Singapore
[3] Natl Univ Singapore Hosp, Dept Diagnost Radiol, Singapore 119074, Singapore
[4] Natl Inst Neurosci, Dept Neuroradiol, Singapore, Singapore
[5] Univ New S Wales, Prince Wales Hosp, Ctr Minimally Invas, Sydney, NSW, Australia
来源：
CHILDS NERVOUS SYSTEM | 2014年 / 30卷 / 02期
关键词：
Congenital pial arteriovenous fistula; Cerebral pediatric arteriovenous malformation; Intraventricular hemorrhage; Hydrocephalus; HEREDITARY HEMORRHAGIC TELANGIECTASIA; ENDOVASCULAR TREATMENT; CHILDREN; MALFORMATIONS; OCCLUSION; OUTCOMES; BRAIN; COILS;
D O I：
10.1007/s00381-013-2217-2
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Intracranial pial arteriovenous fistulas (AVF) are rare vascular malformation especially in the first 2 years of life. The pathology in this age group is associated with greater morbidity and mortality. We report a rare case of 36-day-old male infant with a pial AVF associated with an arterial aneurysm, who presented with intraventricular hemorrhage and hydrocephalus. In addition, an online review of the literatures on pediatric pial AVF was performed using PubMed on published case reports and articles from 1980 to April 2013.
引用
收藏
页码：365 / 369
页数：5
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