Surgical treatment of pediatric moyamoya disease

被引：0

作者：

Rhee, Jay W. ^{[1
]}

Tork, Craig A. ^{[2
]}

Sabbag, Orlando D. ^{[3
]}

Magge, Suresh N. ^{[4
]}

机构：

[1] Georgetown Univ Hosp, Dept Neurosurg, Washington, DC USA

[2] Medstar Washington Hosp Ctr, Washington, DC USA

[3] Georgetown Univ, Sch Med, Arlington, VA USA

[4] Childrens Natl Med Ctr, Div Neurosurg, 111 Michigan Ave NW,4th Floor West Wing,Suite 100, Washington, DC 20010 USA

来源：

JOURNAL OF PEDIATRIC NEURORADIOLOGY | 2014年 / 3卷 / 01期

关键词：

Moyamoya disease; Moyamoya syndrome; Encephaloduroarteriosynangiosis; EDAS; Superficial temporal artery to middle cerebral artery bypass; pial synangiosis; stroke; ischemia;

D O I：

10.3233/PNR-14084

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Cerebral ischemia is a well-recognized cause of morbidity in the pediatric population. Moyamoya disease, first described in 1957 by Takeuchi and Shimizu, is an idiopathic chronic vasculopathy that often presents with ischemia. Moyamoya syndrome presents with similar clinical manifestations and disease progression but may occur unilaterally or in the setting of a predisposing condition. Both direct and indirect revascularization procedures have proven to be efficacious for pediatric moyamoya patients.

引用

页码：29 / 37

页数：9

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