Results 201 to 210 of about 49,976 (250)
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Right lung cancer with right aortic arch
General Thoracic and Cardiovascular Surgery, 2003We report here a case of right lung cancer with right aortic arch. A 67-year-old woman with right aortic arch was found to have a 3-cm squamous cell carcinoma arising in the right middle lobe. Right middle lobectomy with lymphadenectomy was performed via right thoracotomy.
Takashi Kondo +2 more
exaly +3 more sources
American Heart Journal, 1950
Abstract A case of a right-sided aortic arch is presented with angiocardiographic confirmation of the exact type of right-sided arch present.
P, SAMET, D J, STONE
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Abstract A case of a right-sided aortic arch is presented with angiocardiographic confirmation of the exact type of right-sided arch present.
P, SAMET, D J, STONE
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Coarctation of a Right Aortic Arch
Journal of Cardiac Surgery, 2006Right-sided aortic arch with a concomitant coarctation is an exceedingly rare congenital cardiac anomaly. We report of a 4-year-old boy who presented with a history of a stenotic bicuspid aortic valve who upon further evaluation was found to have a coarctation of a right-sided aortic arch. The frequency with which other anomalies exist in either of the
Thomas S, Maxey +4 more
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Retroesophageal right aortic arch
Pediatric Cardiology, 1984Right aortic arch with left descending aorta and a retroesophageal aortic segment is an uncommon congenital vascular malformation which may cause symptoms of compression from a vascular "ring." The presence of this malformation may be suspected by the findings on barium swallow and the diagnosis confirmed by angiocardiography. Surgical intervention may
A, Schneeweiss +4 more
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The right aortic arch revisited
Clinical Radiology, 1991The association between congenital cardiac defects and a right-sided aortic arch was assessed in 900 children undergoing cardiac angiography. Some of the associations observed differ from those reported in the established radiological literature. A right arch occurred in 15% of children with truncus arteriosus (up to 50% quoted in the literature), and ...
D, Glew, G G, Hartnell
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Postgraduate Medicine, 1970
In right aortic arch the branching pattern will be either a mirror image of normal or a partial mirror image characterized by an aberrant left subclavian artery. The chance of associated severe heart defect is 95 percent with mirror-image branching, but only about 10 percent with an aberrant left subclavian artery. A barium esophagram will indicate the
Edward B. D. Neuhauser +1 more
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In right aortic arch the branching pattern will be either a mirror image of normal or a partial mirror image characterized by an aberrant left subclavian artery. The chance of associated severe heart defect is 95 percent with mirror-image branching, but only about 10 percent with an aberrant left subclavian artery. A barium esophagram will indicate the
Edward B. D. Neuhauser +1 more
openaire +2 more sources
Aortic Atresia Combined with Right Aortic Arch
Journal of Cardiac Surgery, 2012We present a case of an aortic atresia and a persistent right aortic arch with a retro-aortic brachiocephalic vein. A left neo-aortic arch was constructed using a reversed subclavian flap and a standard Norwood-type patch enlargement to provide systemic outflow. The intercarotid section of the aortic arch was hypoplastic.
Melchior, Burri +4 more
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Harefuah
A 66-year-old male developed dysphagia due to external compression of the esophagus caused by an aberrant left subclavian artery, as part of a rare congenital anomaly of a right aortic arch. This represents an incomplete vascular ring-an anatomical variant of the right aortic arch - which is typically asymptomatic but may present with swallowing ...
Emil, Sameyah, Gil, Bachar
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A 66-year-old male developed dysphagia due to external compression of the esophagus caused by an aberrant left subclavian artery, as part of a rare congenital anomaly of a right aortic arch. This represents an incomplete vascular ring-an anatomical variant of the right aortic arch - which is typically asymptomatic but may present with swallowing ...
Emil, Sameyah, Gil, Bachar
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Total Arch Replacement for a Distal Aortic Arch Aneurysm With Right Aortic Arch
The Annals of Thoracic Surgery, 2007Right-sided aortic arch accompanied by an aberrant origin of the left subclavian artery is rare and seen in 0.05% approximately 0.1% of the population. A 73-year-old woman with this anomaly was admitted to our institution because of the enlargement of the distal aortic arch aneurysm. She also had mild dysphagia.
Keiko, Kiokawa +5 more
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Radiology, 1936
Right aortic arch is a rare anomaly, the diagnosis of which is seldom established during life. Paradoxically, it is the easiest of all the congenital anomalies of the circulatory system to recognize with certainty. This can be accomplished immediately in practically all cases in which a complete roentgenologic examination of the heart can be made.
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Right aortic arch is a rare anomaly, the diagnosis of which is seldom established during life. Paradoxically, it is the easiest of all the congenital anomalies of the circulatory system to recognize with certainty. This can be accomplished immediately in practically all cases in which a complete roentgenologic examination of the heart can be made.
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