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先天性冠状动脉瘘的有效长期手术治疗。

Effective long-term surgical management of congenital coronary artery fistulas.

机构信息

Department of Cardiovascular Surgery, Tokyo Women's Medical University, Japan.

出版信息

Tohoku J Exp Med. 2011 Mar;223(3):205-9. doi: 10.1620/tjem.223.205.

DOI:10.1620/tjem.223.205
PMID:21372522
Abstract

Congenital coronary artery fistula (CAF) is a rare anomaly involving communication between the coronary artery and any cardiac chamber. We retrospectively studied 23 patients with CAF who were surgically treated at 2 institutes over the past 38 years. All patients had continuous murmur and were diagnosed using echocardiography and cardiac catheterization. Eighteen patients had no other heart anomalies, and 5 had an associated anomaly. Fifteen patients were treated using cardiopulmonary bypass via differential surgical approaches (6 patients, CAF orifice closure through cardiac chamber; 6, coronary arteriotomy for CAF orifice closure; and 3, CAF ligation). Eight patients underwent CAF ligation without cardiopulmonary bypass. CAF originated from the right coronary artery in 11 patients; the left coronary artery in 10, and both arteries in 2. Drainage occurred at the following sites: the right ventricle (10 patients), right atrium (6), left ventricle (4), left atrium (2), and pulmonary artery (1). All surgeries were performed through a median sternotomy. There were no mortalities during or after the hospital stay. Aortic root replacement was performed in 1 patient 30 years after the CAF surgery. Three of the 6 patients who underwent coronary arteriotomy for CAF orifice closure showed coronary artery occlusion at the distal coronary arteriotomy site with long-term collateral formation. Surgical management of CAF was thus effective, resulting in 100% long-term survival and closure rates. Dilated CAF-associated vessels have been normalized for the long term. CAF should be therefore considered even in asymptomatic patients because of the risk of future complications.

摘要

先天性冠状动脉瘘(CAF)是一种罕见的异常情况,涉及冠状动脉与任何心腔之间的沟通。我们回顾性研究了过去 38 年在 2 个机构接受手术治疗的 23 例 CAF 患者。所有患者均有连续性杂音,并通过超声心动图和心导管检查进行诊断。18 例患者无其他心脏异常,5 例患者存在相关异常。15 例患者采用心肺转流术通过不同的手术方法进行治疗(6 例患者通过心腔闭合冠状动脉瘘口;6 例患者通过冠状动脉切开术闭合冠状动脉瘘口;3 例患者通过结扎冠状动脉瘘口)。8 例患者在无体外循环的情况下进行了冠状动脉瘘结扎术。冠状动脉瘘口起源于右冠状动脉 11 例;左冠状动脉 10 例,左右冠状动脉各 2 例。引流部位如下:右心室(10 例)、右心房(6 例)、左心室(4 例)、左心房(2 例)和肺动脉(1 例)。所有手术均通过正中胸骨切开术进行。在住院期间或之后,没有死亡病例。1 例患者在冠状动脉瘘手术后 30 年时进行了主动脉根部置换术。6 例接受冠状动脉切开术闭合冠状动脉瘘口的患者中,有 3 例出现远端冠状动脉切开处的冠状动脉闭塞,长期形成侧支循环。因此,CAF 的手术治疗是有效的,长期存活率和闭合率达到 100%。长期来看,扩张的 CAF 相关血管已经恢复正常。因此,即使无症状患者也应考虑 CAF,因为存在未来并发症的风险。

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引用本文的文献

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Case Report: Isolate Congenital Coronary Artery Fistula With Giant Artery Aneurysm in a Neonate.病例报告:新生儿孤立性先天性冠状动脉瘘合并巨大动脉动脉瘤
Front Cardiovasc Med. 2021 Jun 16;8:633840. doi: 10.3389/fcvm.2021.633840. eCollection 2021.
2
Congenital coronary artery fistula in pediatric patients: transcatheter versus surgical closure.小儿先天性冠状动脉瘘:介入治疗与外科治疗的对比。
BMC Cardiovasc Disord. 2020 Nov 16;20(1):484. doi: 10.1186/s12872-020-01769-7.
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Right coronary artery fistula misdiagnosed as right atrial cardiac myxoma: A case report.
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Oncol Lett. 2016 Jun;11(6):3715-3718. doi: 10.3892/ol.2016.4457. Epub 2016 Apr 19.
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A Giant Left Main Trunk and Left Circumflex Artery-to-Right Ventricle Fistula.巨大的左主干及左旋支动脉至右心室瘘
Heart Views. 2014 Apr;15(2):51-3. doi: 10.4103/1995-705X.137501.
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An uncommon anatomy presenting with a common disease.一种罕见的解剖结构表现为一种常见疾病。
BMJ Case Rep. 2012 Sep 7;2012:bcr-2012-006189. doi: 10.1136/bcr-2012-006189.