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右位主动脉弓伴食管后左锁骨下动脉及肺动脉起源于主动脉异常

Right Aortic Arch with a Retroesophageal Left Subclavian Artery and an Anomalous Origin of the Pulmonary Artery from the Aorta.

作者信息

Jeon Chang-Seok, Shim Man-Shik, Yang Ji-Hyuk, Jun Tae-Gook

机构信息

Department of Thoracic and Cardiovascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine.

出版信息

Korean J Thorac Cardiovasc Surg. 2017 Feb;50(1):44-46. doi: 10.5090/kjtcs.2017.50.1.44. Epub 2017 Feb 5.

DOI:10.5090/kjtcs.2017.50.1.44
PMID:28180103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5295483/
Abstract

We report the case of a newborn with a rare anatomic variation: a right aortic arch with a retroesophageal left subclavian artery and an anomalous origin of the pulmonary artery from the aorta. This variation was diagnosed using echocardiography and computed tomography, and we treated the condition surgically.

摘要

我们报告了一例患有罕见解剖变异的新生儿病例

右位主动脉弓伴食管后左锁骨下动脉以及肺动脉起源于主动脉异常。这种变异通过超声心动图和计算机断层扫描得以诊断，并且我们对该病症进行了手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb7/5295483/517b678bacd5/kjtcvs-50-044f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb7/5295483/7426764d18ec/kjtcvs-50-044f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb7/5295483/517b678bacd5/kjtcvs-50-044f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb7/5295483/7426764d18ec/kjtcvs-50-044f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb7/5295483/517b678bacd5/kjtcvs-50-044f2.jpg

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本文引用的文献

1
Right aortic arch with aberrant left subclavian artery and anomalous origin of right pulmonary artery from ascending aorta.右位主动脉弓伴左锁骨下动脉异常及右肺动脉起自升主动脉异常。
World J Pediatr Congenit Heart Surg. 2011 Apr;2(2):324-6. doi: 10.1177/2150135110389830.
2
Right aortic arch and its variants.右位主动脉弓及其变异。
J Cardiovasc Comput Tomogr. 2010 Sep-Oct;4(5):293-300. doi: 10.1016/j.jcct.2010.07.002. Epub 2010 Jul 21.
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Incomplete double aortic arch with atresia of the distal left arch: distinctive imaging appearance.
不完全性双主动脉弓伴左弓远端闭锁：独特的影像学表现。
AJR Am J Roentgenol. 2005 May;184(5):1634-9. doi: 10.2214/ajr.184.5.01841634.
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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.与22号染色体间质q11缺失相关的临床特征谱：一项欧洲合作研究。
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A case of the incomplete double aortic arch diagnosed in adulthood by MR imaging.一例成年期通过磁共振成像诊断出的不完全性双主动脉弓病例。
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Surgical repair of coarctation of the aorta in infants under one year of age. Long-term results in 146 patients comparing subclavian flap angioplasty and modified end-to-end anastomosis.
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