Pulmonary arteriovenous malformations

被引:50
作者
Tellapuri, Sreeshma [1 ]
Park, Harold S. [1 ]
Kalva, Sanjeeva P. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Radiol, Div Intervent Radiol, Dallas, TX 75390 USA
关键词
Pulmonary arteriovenous malformation (PAVM); Embolization; Endovascular therapy; Coil; Microvascular plug; Hereditary hemorrhagic telangiectasia (HHT); HEREDITARY HEMORRHAGIC TELANGIECTASIA; CONTRAST ECHOCARDIOGRAPHY; HEPATOPULMONARY SYNDROME; MR-ANGIOGRAPHY; CT; EMBOLIZATION; ANGIOARCHITECTURE; EMBOLOTHERAPY; FISTULAS; MANAGEMENT;
D O I
10.1007/s10554-018-1479-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in 50% individuals, it can present with the dreaded complications of stroke or intracranial abscess in high-risk individuals including pregnant women, if untreated. The mainstay of treatment is now endovascular embolization of the feeding artery which can alleviate the symptoms and prevent these complications. In this review, we describe the pathophysiology, methods of screening, diagnostic workup and treatment of these vascular lesions with a particular focus on the currently used embolization techniques and their outcomes.
引用
收藏
页码:1421 / 1428
页数:8
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