Atypical Presentation of a Large Aortopulmonary Window in a Very Low Weight and Preterm Born Infant

Katja Schumacher, Sabine Meier, M. Borger, M. Kostelka, M. Vollroth
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Abstract

of a Large Aortopulmonary Window in a Very Low Weight and Preterm Born Infant. 370-373. Abstract Background Aortopulmonary window represents 0.2-0.3% of all congenital cardiac malformations. Usually, aortopulmonary window results in left-to-right shunt. Thus, progressive pulmonary hypertension and its consequences are associated with this anomaly. Commonly, it is located in the ascending aorta. Case Presentation We are describing a premature low-birth-weight infant who was diagnosed with large aortopulmonary window between the pulmonary artery bifurcation and the ascending aorta extending to the aortic arch. Surgery was successfully performed at the age of 4 weeks due to progressive congestive heart failure. This report highlights the importance of early surgical repair in patients with complex aortopulmonary window configuration.
极低体重早产儿主动脉肺窗大的不典型表现
极低体重早产儿大主动脉肺窗的研究。370-373。主动脉肺窗占所有先天性心脏畸形的0.2-0.3%。通常,主动脉肺窗导致左向右分流。因此,进行性肺动脉高压及其后果与这种异常有关。通常,它位于升主动脉。我们报告了一个早产的低出生体重婴儿,他被诊断为肺动脉分叉和升主动脉延伸到主动脉弓之间的大主动脉肺窗。由于进行性充血性心力衰竭,手术在4周大时成功进行。本报告强调了早期手术修复复杂主动脉肺窗结构患者的重要性。
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