Aberrant right retroesophageal subclavian artery causing esophageal compression

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Aberrant right retroesophageal subclavian artery causing esophageal compression

Dysphagia lusoria is present in 0.2-2.5% of the population representing the most common anomaly of the aortic arch (De Araújo et al., 2015, Int. J. Surg. Case Rep., 7, 32). It usually presents in infants, but can present at any age. Symptoms include cough, dysphagia, thoracic pain, and pulmonary infection. Barium contrast studies, CT, and MR angiography are useful studies for evaluating the con...

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Three cases of retroesophageal right subclavian artery.

We have experienced three cases of retroesophageal right subclavian artery. Two cases were cadavers, and one case was a live human. In the two cadavers of a 68-year-old and a 76-year-old, respectively Japanese and European males, the right subclavian artery originated from the aorta after the aorta branched the right carotid artery, the left carotid artery and the left subclavian artery. The ri...

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Right subclavian steal associated with aberrant right subclavian artery.

The subclavian steal syndrome is a well-recognized clinical and radiographic entity that involves the left subclavian artery far more commonly than the right. Atherosclerotic stenoses are the most common underlying cause [1-3]. Right subclavian stenosis with associated steal is markedly less common. Although an aberrant right subclavian artery is one of the most common anomalies of the great ve...

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Arch of aorta with bi-carotid trunk, left subclavian artery, and retroesophageal right subclavian artery.

We report a case of left sided aortic arch with three branches - a bi-carotid trunk, left subclavian, artery and right subclavian artery. The anomalous right subclavian artery presented a retroesophageal course. A right non-recurrent laryngeal nerve was noticed. The embryonic development of this branching pattern is discussed.

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Aberrant right subclavian artery and right-sided ductus arteriosus.

DESCRIPTION A premature newborn weighing 1.9 kg, presenting with cyanosis, feeding and respiratory difficulties was admitted to our centre for further evaluation. An initial echocardiogram suggested a pulmonary atresia with a malalignment infundibular ventricle septum defect with atypical right-sided ductus arteriosus (2.4 mm) arising from the aberrant right subclavian artery (4 mm), which was ...

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ژورنال

عنوان ژورنال: Clinical Case Reports

سال: 2015

ISSN: 2050-0904,2050-0904

DOI: 10.1002/ccr3.351