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左冠状动脉先天性闭锁——两名儿童的心肌血运重建

Congenital atresia of the left coronary artery--myocardial revascularization in two children.

作者信息

Gebauer Roman, Cerny Stepan, Vojtovic Pavel, Tax Petr

机构信息

Kardiocentrum and Cardiovascular Research Centre, University Hospital Motol, Prague, Czech Republic.

出版信息

Interact Cardiovasc Thorac Surg. 2008 Dec;7(6):1174-5. doi: 10.1510/icvts.2008.184317. Epub 2008 Aug 26.

Abstract

Two patients with congenital atresia of the left coronary artery ostium underwent myocardial revascularization at the age of three years and three months, respectively. The patients were admitted to the hospital with a clinical history of sudden chest pain or short apnea not necessitating resuscitation. Non-invasive examinations and hemodynamic studies revealed dysfunction of the left ventricle and ostial atresia of the left coronary artery. Surgical revascularization-bypass grafts were performed using the left internal mammary artery and saphenous vein graft in the first case and the left internal mammary artery in the second child. Both patients survived surgery and good patency of the grafts was confirmed by coronary angiograms during hospital stay. These cases are interesting because of their rarity and diagnostic and therapeutic difficulties.

摘要

两名左冠状动脉口先天性闭锁患者分别在三岁零三个月时接受了心肌血运重建术。这两名患者因突发胸痛或短暂呼吸暂停的临床病史入院,无需进行复苏。非侵入性检查和血流动力学研究显示左心室功能障碍和左冠状动脉口闭锁。第一例手术采用左乳内动脉和大隐静脉移植进行血运重建搭桥手术,第二例患儿采用左乳内动脉。两名患者均手术存活,住院期间冠状动脉造影证实移植血管通畅良好。这些病例因其罕见性以及诊断和治疗困难而令人关注。

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