双肺移植患者肺动脉动脉瘤合并严重肺动脉高压:一种罕见疾病的回顾和经食管超声心动图的作用。

IF 1.1 Q3 ANESTHESIOLOGY
Faisal D Arain, Victoria A Gilbride
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引用次数: 1

摘要

肺动脉动脉瘤(PAA)是一种罕见的疾病,在病因不明的情况下,可分为先天性、获得性或特发性。当合并严重的特发性肺动脉高压时,这种PAA病例可能作为肺移植的指征出现在手术室。在这篇文章中,我们提出了这样一个病例,患者有一个巨大的主、右PAA,接受双肺移植。我们描述了这种PAA的病理生理和自然过程,并讨论了术中经食管超声心动图在治疗这种罕见诊断患者中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary Artery Aneurysm Associated With Severe Pulmonary Hypertension in a Patient Presenting for Double Lung Transplant: Review of a Rare Disorder and Role of Transesophageal Echocardiography.

Pulmonary artery aneurysm (PAA) is a rare disorder that may be classified as congenital, acquired, or idiopathic, in the case of unclear etiology. When associated with severe idiopathic pulmonary arterial hypertension, such a case of PAA may present to the operating room as an indication for lung transplantation. In this article, we present such a case of a patient with a giant main and right PAA that underwent a double lung transplant. We describe the pathophysiology and natural course of this PAA and discuss the role of intraoperative transesophageal echocardiography in the management of patients with this rare diagnosis.

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来源期刊
CiteScore
3.60
自引率
14.30%
发文量
31
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