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一名右乳内动脉移植物起源于右迷走锁骨下动脉患者的直接经皮冠状动脉介入治疗

Primary percutaneous coronary intervention in a patient with right internal mammary artery graft originating from arteria lusoria dextra.

作者信息

Aleksandrić Srdjan, Stojković Siniša, Tomašević Miloje, Kostić Jelena, Banović Marko, Menković Nemanja, Ostojić Miodrag

机构信息

University of Belgrade, Serbia.

出版信息

Srp Arh Celok Lek. 2013 Mar-Apr;141(3-4):223-7. doi: 10.2298/sarh1304223a.

DOI:10.2298/sarh1304223a
PMID:23745348
Abstract

INTRODUCTION

Congenital aomalies of the aortic arch, although numerous and heterogeneous, occur in less than 1% of individuals at autopsies. Left aortic arch with an aberrant right subclavian artery, also called arteria lusoria dextra, is the most common anomaly of the aortic arch, occurring in 0.5-2.5% of individuals.

CASE OUTLINE

We report the case of a 48-year-old man suffering from acute inferoposterior-wall ST elevation myocardial infarction successfully treated by primary percutaneous coronary intervention.Ten years ago, the patient had undergone coronary artery bypass graft surgery with the implantation of two arterial grafts- left and right internal mammary arteries on both left anterior descending and right coronary artery. After several attempts to canulate truncus brachiocephalicus, angiogram revealed the left aortic arch with the aberrant right subclavian artery. To our knowledge, this is the first described case of primary percutaneous coronary intervention via the aberrant right subclavian artery and right internal mammary artery graft with stent implantation in the infarct related lesion of the distal segment of right coronary artery. Subsequent 64-multidetector computed tomography confirmed the angiographic findings.

CONCLUSION

Early recognition of congenital anomalies of the aortic arch and its great vessels, even before coronary artery bypass graft surgery, could be crucial for the urgent and successful treatment of patients with life-threatening conditions, such as ST segment elevation myocardial infarction.

摘要

引言

主动脉弓先天性异常虽然种类繁多且各不相同,但在尸检中的发生率不到1%。左主动脉弓伴迷走右锁骨下动脉,也称为右迷走动脉,是主动脉弓最常见的异常,发生率为0.5% - 2.5%。

病例概述

我们报告了一名48岁男性急性下后壁ST段抬高型心肌梗死患者,通过直接经皮冠状动脉介入治疗成功治愈。十年前,该患者接受了冠状动脉旁路移植手术,在左前降支和右冠状动脉上分别植入了两支动脉移植物——左、右乳内动脉。在多次尝试插管头臂干失败后,血管造影显示为左主动脉弓伴迷走右锁骨下动脉。据我们所知,这是首例经迷走右锁骨下动脉和右乳内动脉移植物进行直接经皮冠状动脉介入治疗,并在右冠状动脉远端梗死相关病变处植入支架的病例。随后的64排多层螺旋CT证实了血管造影结果。

结论

即使在冠状动脉旁路移植手术之前,早期识别主动脉弓及其大血管的先天性异常,对于危及生命状况(如ST段抬高型心肌梗死)患者的紧急和成功治疗可能至关重要。

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