Pulmonary arteriovenous malformations and their mimics

被引:51
作者
Gill, S. S. [1 ]
Roddie, M. E. [1 ]
Shovlin, C. L. [2 ]
Jackson, J. E. [1 ]
机构
[1] Imperial Coll Healthcare NHS Trust, Dept Imaging, London W12 0HS, England
[2] Univ London Imperial Coll Sci Technol & Med, NHLI Cardiovasc Sci, London, England
关键词
HEREDITARY HEMORRHAGIC TELANGIECTASIA; TO-LEFT SHUNT; HELICAL CT; FOLLOW-UP; EMBOLIZATION; EMBOLOTHERAPY; PSEUDOANEURYSMS; HYPERTENSION;
D O I
10.1016/j.crad.2014.09.003
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 communications between, the pulmonary arteries and veins, which. result in a right-to-left (R L) shunt with resultant hypoxemia, the severity of which will depend upon the size and number of lesions. Most PAVMs occur in individuals with hereditary haemorrhagic telangiectasia (HHT) and are a cause of serious morbidity and mortality largely related to cerebrovascular complications secondary to paradoxical embolization. The importance of their recognition and treatment by embolization, even in the absence of symptoms, is well known. Their appearances on chest radiographs are often, but not always, characteristic and the CT appearances are diagnostic; however, there are a number of both vascular and non-vascular diseases that can cause confusion. This review serves to highlight these PAVM "mimics". (C) 2014 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:96 / 110
页数:15
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