Angioarchitecture of Hereditary Arteriovenous Malformations

被引:6
|
作者
Burrows, Patricia E. [1 ]
机构
[1] Med Coll Wisconsin, Childrens Hosp Wisconsin, Dept Radiol, 9000 West Wisconsin Ave,MS 721, Milwaukee, WI 53226 USA
关键词
arteriovenous malformation; capillary malformation-arteriovenous malformation; hereditary hemorrhagic telangiectasia; PTEN tumor hamartoma syndrome; genetic mutations; HEPATIC VASCULAR MALFORMATIONS; RILEY-RUVALCABA-SYNDROME; HEMORRHAGIC TELANGIECTASIA; IMAGING FINDINGS; RASA1; MUTATIONS; PTEN MUTATIONS; EMBOLIZATION; CHILDREN; RISK; MANAGEMENT;
D O I
10.1055/s-0037-1604298
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
This article describes three hereditary conditions known to be associated with arteriovenous malformation (AVM), along with their clinical and imaging features and angiographic angioarchitecture. Hereditary hemorrhagic telangiectasia, capillary malformation AVM (CM AVM), and PTEN tumor hamartoma syndrome are conditions with autosomal dominant inheritance, caused by mutations in different molecular pathways, which frequently present with symptomatic AVMs. Imaging biomarkers, including sites of predilection, angioarchitecture, and tissue overgrowth patterns, are helpful in identifying these patients and selecting appropriate treatment.
引用
收藏
页码:250 / 257
页数:8
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