经导管限制孤立性非冗余主动脉-肺侧枝血流1例报告。

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
European Heart Journal: Case Reports Pub Date : 2025-09-02 eCollection Date: 2025-09-01 DOI:10.1093/ehjcr/ytaf426
Nandini Mehra, Hani Najm, Justin Tretter, Nicholas Szugye, Joanna Ghobrial
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引用次数: 0

摘要

背景:主要的主动脉-肺动脉副动脉是供应肺部的节段性动脉的先天性残余。它们通常与先天性心脏病有关,特别是在肺动脉主干分支不发达的情况下,这些节段性侧枝不退化,继续向肺血管供应含氧血液。随着时间的推移,这些侧络会出现问题,特别是当它们扩大时,会导致咯血、节段性肺动脉高压和左心容量过载等临床症状。病例总结:在此,我们描述了一个罕见的病例孤立的主要主动脉-肺侧支没有相关的先天性心脏病,表现为咯血,并经皮处理改良的血流减少装置。讨论:对于这种非常独特的临床情况,这是一种新的治疗方法。在讨论本病例时,采用多学科讨论和以患者为中心的共同决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Case report of transcatheter flow restriction in isolated non-redundant major aorto-pulmonary collateral arteries.

Case report of transcatheter flow restriction in isolated non-redundant major aorto-pulmonary collateral arteries.

Case report of transcatheter flow restriction in isolated non-redundant major aorto-pulmonary collateral arteries.

Case report of transcatheter flow restriction in isolated non-redundant major aorto-pulmonary collateral arteries.

Background: Major aorto-pulmonary collateral arteries are congenital remnants of the segmental arteries that supply the lungs. They are commonly associated with congenital heart disease, particularly in cases where the main pulmonary artery branches are not well developed, these segmental collaterals do not regress and continue to supply oxygenated blood to the pulmonary vasculature. Over time, these collaterals can become problematic, particularly if they enlarge, leading to clinically significant symptoms such as haemoptysis, segmental pulmonary hypertension, and left heart volume overload.

Case summary: Herein, we describe a rare case of isolated major aorto-pulmonary collaterals without associated congenital heart disease that presented with haemoptysis and managed percutaneously with a modified flow-reducer device.

Discussion: This is a novel therapy for this very unique clinical scenario. Both multidisciplinary discussion and patient centred shared decision-making were utilized while discussing this case.

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来源期刊
European Heart Journal: Case Reports
European Heart Journal: Case Reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
10.00%
发文量
451
审稿时长
14 weeks
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