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一名有症状的迷走右锁骨下动脉且头臂干缺如患者的诊断挑战

Diagnostic Challenge in a Symptomatic Patient of Arteria Lusoria with Retro-esophageal Right Subclavian Artery and Absent Brachiocephalic Trunk.

作者信息

Akbar Hina, Kahloon Arslan, Kahloon Rehan

机构信息

Internal Medicine and Hospital Medicine, The University of Tennessee Health Science Center (UTHSC), Memphis, USA.

Gastroenterology, Erlanger Health System/UT College of Medicine, Chattanooga, USA.

出版信息

Cureus. 2020 Feb 18;12(2):e7029. doi: 10.7759/cureus.7029.

Abstract

A combination of absent brachiocepahlic trunk and anomalous left circumflex artery with a retro-esophageal right subclavian artery is an extremely rare finding. This can clinically manifest as episodic dysphagia and chest pain. Routine coronary angiography via femoral access could be misleading and right radial access in such cases can be particularly challenging and has never been reported in literature before. We present a case of a 42-year-old female with symptoms of chest, back, and left neck pain. She also complained of occasional dysphagia, dizziness, and palpitations. Physical examination revealed a regular heart rhythm with no vascular bruits. An electrocardiogram (EKG) only showed normal sinus rhythm and incomplete right bundle branch block. Noninvasive testing included an echocardiogram and previously done exercise stress test, and myocardial perfusion scans were noted to be normal. A diagnostic cardiac catheterization via right radial approach was performed to delineate her coronary anatomy and rule out ischemic etiology. This led to diagnosis of anomalous coronary anatomy (retro-esophageal right subclavian artery arising from descending aorta in association with an anomalous right circumflex artery with absent innominate artery) through a technically difficult and risky procedure. Significant vessel tortuosity and abnormal catheter angulations were encountered and were overcome by using specific catheters. Meticulous use of 6 French MP, WR, JL, and JR4 catheters along with an exchange length wire was required to negotiate the anatomical variations and complete the coronary angiogram via right radial artery. From a procedural stand-point, coronary angiography via right radial access in presence of such rare anatomical variations can be particularly challenging. Routine femoral catheterization may fail to depict this important anatomical variation. Coronary angiogram via right radial access in the presence of a combination of anatomical variations of great vessels and anomalous coronary arteries is particularly challenging from a procedural stand point due to vessel tortuosity and shape of catheters. Choice of anatomically appropriate diagnostic catheters and specific maneuvers are imperative in these coronary angiographic procedures.

摘要

头臂干缺如、左旋支动脉异常合并食管后右锁骨下动脉是一种极其罕见的情况。这在临床上可表现为发作性吞咽困难和胸痛。经股动脉途径进行常规冠状动脉造影可能会产生误导,而在此类病例中经右桡动脉途径操作极具挑战性,且此前文献中从未有过报道。我们报告一例42岁女性,有胸部、背部和左颈部疼痛症状。她还主诉偶尔出现吞咽困难、头晕和心悸。体格检查显示心律规则,无血管杂音。心电图(EKG)仅显示正常窦性心律和不完全性右束支传导阻滞。无创检查包括超声心动图和之前做过的运动负荷试验,心肌灌注扫描结果正常。通过右桡动脉途径进行诊断性心导管检查,以明确其冠状动脉解剖结构并排除缺血性病因。通过一项技术难度大且有风险的操作,诊断为冠状动脉解剖异常(食管后右锁骨下动脉发自降主动脉,合并无名动脉缺如的异常右回旋支动脉)。术中遇到明显的血管迂曲和异常的导管成角情况,通过使用特定导管得以克服。需要精细使用6F的MP、WR、JL和JR4导管以及交换长度导丝来应对解剖变异,经右桡动脉完成冠状动脉造影。从操作角度来看,在存在此类罕见解剖变异的情况下经右桡动脉进行冠状动脉造影极具挑战性。常规股动脉导管检查可能无法显示这一重要的解剖变异。由于血管迂曲和导管形状,在存在大血管解剖变异和冠状动脉异常合并情况时经右桡动脉进行冠状动脉造影,从操作角度来看尤其具有挑战性。在这些冠状动脉造影操作中,选择解剖结构合适的诊断导管和特定操作至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3207/7029822/2b71d108535b/cureus-0012-00000007029-i01.jpg

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