Management of pulmonary arteriovenous malformations.
Management of pulmonary arteriovenous malformations.
复制标题
DOI：
10.1055/s-0031-1273937
复制
发表时间：
2011-03-01
影响因子：
1.4
通讯作者：
Beheshti, Michael V
中科院分区：
文献类型：
--
作者：
Meek, Mary E;Meek, James C;Beheshti, Michael V
肺动静脉畸形是罕见的病变，具有显着的临床并发症。这些病变常见于遗传性出血性毛细血管扩张症（以前称为奥斯勒-韦伯-伦杜综合征）患者。介入放射科医生是这种复杂疾病治疗团队的关键组成部分，彻底了解疾病过程对于提供良好的患者护理至关重要。在本文中，作者回顾了病程及其与遗传性出血性毛细血管扩张症的关联，讨论了这些复杂患者的临床评估和治疗，并概述了并发症和随访。
Pulmonary arteriovenous malformations are rare lesions with significant clinical complications. These lesions are commonly seen in patients with hereditary hemorrhagic telangiectasia (formerly Osler-Weber-Rendu syndrome). Interventional radiologists are a key part of the treatment team in this complex disease, and a thorough understanding of the disease process is critical to providing good patient care. In this article, the authors review the disease course and its association with hereditary hemorrhagic telangiectasia, discusses the clinical evaluation and treatment of these complex patients, and outlines complications and follow-up.