伴有劳勃里-佩齐综合征的主动脉-肺动脉瘘:诊断之谜

Assia Elouardi , Mohammed Messouak
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引用次数: 0

摘要

主动脉肺动脉瘘通常是在死后被诊断出来的,是一种非常罕见的疾病,通常具有很高的致死率。在这里,我们介绍一例独特的病例,患者 29 岁,无主动脉瘤病史或既往主动脉手术史,因劳勃里-佩齐综合征转诊接受手术治疗,术中发现升主动脉与主肺动脉之间存在主动脉-肺动脉瘘。患者手术成功,术后恢复顺利。我们的病例是首次报道主动脉-肺动脉瘘同时合并劳勃里-佩齐综合征的病例。该病例的独特之处包括:由于隐匿性左心室容量超负荷,患者在数月内出现心力衰竭;与已知的心内分流并存,诊断具有挑战性,强调了提高警惕的必要性;尽管发病率和死亡率较高,但手术仍取得了成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aorto-pulmonary artery fistula with Laubry-Pezzi syndrome: A diagnostic enigma

Usually diagnosed post-mortem, aortopulmonary artery fistula is an exceptionally rare and often highly lethal condition. Here, we present a unique case of a 29-year-old woman with no history of aortic aneurysm or previous aortic surgery, referred for surgical management of Laubry-Pezzi syndrome in whom an aorto-pulmonary artery fistula bridging the ascending aorta and the main pulmonary artery was discovered intra operatively. The patient was successfully managed with an uneventful postoperative recovery. Our case outlines the inaugural reported occurrence of an aortopulmonary artery fistula coinciding with Laubry-Pezzi syndrome. Unique features include subtle onset of heart failure over months due to occult left ventricular volume overload, challenging diagnosis alongside known intracardiac shunts, emphasizing the need for vigilance, and demonstration of successful surgical outcomes despite high morbidity and mortality.

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