Pulmonary Arteriovenous Malformations: What the Interventional Radiologist Should Know

被引:6
|
作者
Kaufman, Claire S. [1 ]
McDonald, Jamie [2 ]
Balch, Heather [3 ]
Whitehead, Kevin [4 ]
机构
[1] Oregon Hlth & Sci Univ, Dotter Dept Intervent Radiol, Pacific Northwest HHT Ctr Excellence, Portland, OR 97201 USA
[2] Univ Utah, Dept Pathol, Salt Lake City, UT USA
[3] Univ Utah, HHT Ctr Excellence, Dept Internal Med, Salt Lake City, UT USA
[4] Univ Utah, HHT Ctr Excellence, Div Cardiovasc Med, Salt Lake City, UT USA
关键词
hereditary hemorrhagic telangiectasia; pulmonary arteriovenous malformation; embolization; interventional radiology; HEREDITARY HEMORRHAGIC TELANGIECTASIA; AMPLATZER VASCULAR PLUG; TO-LEFT SHUNT; CONTRAST ECHOCARDIOGRAPHY; FOLLOW-UP; MR-ANGIOGRAPHY; JUVENILE POLYPOSIS; EMBOLIZATION; EMBOLOTHERAPY; FEASIBILITY;
D O I
10.1055/s-0042-1751260
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
Pulmonary arteriovenous malformations (PAVMs) are abnormal connections between the pulmonary artery and pulmonary vein bypassing the normal capillary bed causing a right-to-left shunt. The majority (80-90%) of PAVMs are associated with hereditary hemorrhagic telangiectasia (HHT). PAVMs may be asymptomatic or present with symptoms of hypoxia, shortness of breath, migraines, sequelae of paradoxical embolization, or rupture. Transcatheter embolization has become the standard of care. This article will review the clinical presentation, workup, genetics, imaging findings, embolization, complications, and follow-up for patients with PAVMs.
引用
收藏
页码:261 / 270
页数:10
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