Transcatheter closure of a pulmonary arteriovenous malformation in a patient with hereditary hemorrhagic telangiectasia

被引：0

作者：

Parker C. ^{[2
]}

Rousan T.A. ^{[1
]}

Abu-Fadel M. ^{[1
]}

机构：

[1] Section of Cardiovascular Disease, University of Oklahoma Health Sciences Center and Department of Veterans Affairs Medical Center, 920 Stanton L. Young Boulevard, Williams Pavilion 3010, Oklahoma City, 73104, OK

[2] Department of Internal Medicine, University of Oklahoma Health Sciences Center and Department of Veterans Affairs Medical Center, Oklahoma City, OK

来源：

Cardiovascular Intervention and Therapeutics | 2015年 / 30卷 / 3期

关键词：

Hereditary Hemorrhagic Telangiectasia; Amplatzer Vascular Plug; Compute Tomography Angiogram; Pulmonary Arteriovenous Malformation; Mixed Venous Saturation;

D O I：

10.1007/s12928-014-0276-2

中图分类号：

学科分类号：

摘要：

Pulmonary arteriovenous malformations (PAVM) are rare pulmonary vascular anomalies. Over 50 % of the cases are associated with hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu Syndrome. Untreated PAVMs progressively enlarge and can cause significant right-to-left shunting. Surgical- and catheter-based approaches have been used in the management of PAVM. We report a case of a 74-year-old man who presented with dyspnea and hypoxia and was found to have a large right-sided PAVM. He underwent percutaneous closure of the PAVM with an Amplatzer device with significant improvement of his symptoms. © 2014, Japanese Association of Cardiovascular Intervention and Therapeutics.

引用

页码：270 / 272

页数：2

共 10 条

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