成人孤立性单侧肺动脉缺失(UAPA):在单纯咳嗽和重症监护之间

F. Jacob, F. Vogt, E. Stahlberg, T. Oechtering, S. Anton, M. Planert, S. Schierholz, J. Barkhausen, A. Frydrychowicz
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摘要

单侧肺动脉缺失(UAPA)是一种罕见的先天性疾病,单独发生或与其他先天性心脏缺陷(CHD)一起发生。虽然非孤立性UAPA大多在生命早期被检测到,但孤立性UAPA的检测往往由于多种不特异性症状而延迟。虽然对年轻有症状患者的治疗策略有共识,但在年轻或成人无症状患者中偶然发现UAPA是一个持续争论和有限证据的问题。在这里,我们将提出两个以前未发表的,说明性的不同程度的症状严重的情况下,并讨论确定一个适当的治疗策略的困难。随着病例,我们将回顾文献,目前的典型症状和可能的陷阱,并提供治疗方案的概述,重点是成人患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated Unilateral Absence of Pulmonary Artery (UAPA) in the Adult:Between Simple Cough and Intensive Care
Unilateral absence of pulmonary artery (UAPA) is a rare congenital condition occurring isolated or in conjunction with other congenital heart defects (CHD). While none-isolated UAPA is mostly detected early in life, detection of isolated UAPA is often delayed due to diverse and unspecific symptoms. While there is consensus on the therapeutic strategy in young symptomatic patients, the incidental finding of UAPA in young or adult asymptomatic patients is a matter of on-going debate and limited evidence. Here, we will present two previously unpublished, illustrative cases with different extent of symptom severity and discuss the difficulties in determining an appropriate therapeutic strategy. Along with the cases, we will review the literature, present typical symptoms and possible pitfalls, and provide an overview of therapeutic options with a focus on the adult patient.
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