Results 221 to 230 of about 9,223 (251)
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An Aneurysm of Right-Sided Aortic Arch With Mirror-Image Brachiocephalic Branching
Journal of Thoracic Imaging, 2005The patient is a 63-year-old man whose right retroesophageal aortic arch with mirror-image braciocephalic branching was discovered incidentally on computer tomography (CT), performed after a minor motor vehicle accident 12 years ago. The size of the aortic arch was normal at that time. The patient had no other congenital cardiac anomalies.
Lev, Khitin +3 more
exaly +3 more sources
CardioVascular and Interventional Radiology, 1978
Two patients with a right aortic arch, right patent ductus arteriosus, and mirror-image branching of the brachiocephalic vessels are described. The clinical, angiographic, and surgical findings in these two cases are detailed, and a description of the embryologic basis for these anomalies is given.
Elizabeth A Fisher
exaly +3 more sources
Two patients with a right aortic arch, right patent ductus arteriosus, and mirror-image branching of the brachiocephalic vessels are described. The clinical, angiographic, and surgical findings in these two cases are detailed, and a description of the embryologic basis for these anomalies is given.
Elizabeth A Fisher
exaly +3 more sources
Pediatric Radiology, 1995
An unusual case is presented of a vascular ring due to a right arch with mirror-image branching and a left ligamentum arteriosum from the descending aorta to the left pulmonary artery. There have been only four previous reports of this rare arch anomaly.
A E Schlesinger +2 more
exaly +3 more sources
An unusual case is presented of a vascular ring due to a right arch with mirror-image branching and a left ligamentum arteriosum from the descending aorta to the left pulmonary artery. There have been only four previous reports of this rare arch anomaly.
A E Schlesinger +2 more
exaly +3 more sources
The National Medical Journal of India, 2018
An isolated right-sided aortic arch with no congenital heart disease is extremely rare. We report an adult woman with longstanding rheumatic heart disease causing severe calcific mitral stenosis, moderate mitral regurgitation and moderate pulmonary hypertension, for which she underwent mitral valve replacement and tricuspid annuloplasty.
Sanjay Ganapathi +2 more
exaly +3 more sources
An isolated right-sided aortic arch with no congenital heart disease is extremely rare. We report an adult woman with longstanding rheumatic heart disease causing severe calcific mitral stenosis, moderate mitral regurgitation and moderate pulmonary hypertension, for which she underwent mitral valve replacement and tricuspid annuloplasty.
Sanjay Ganapathi +2 more
exaly +3 more sources
British Journal of Radiology, 1973
Abstract Three patients with right aortic arch and mirror-image branching of the major arteries are presented. In contrast to those reported in the literature, none had associated cardiac defects and all of them had severe symptoms resulting from vascular ring, which required surgical treatment.
Maurice M Aygen, Morris J Levy, B Vidne
exaly +3 more sources
Abstract Three patients with right aortic arch and mirror-image branching of the major arteries are presented. In contrast to those reported in the literature, none had associated cardiac defects and all of them had severe symptoms resulting from vascular ring, which required surgical treatment.
Maurice M Aygen, Morris J Levy, B Vidne
exaly +3 more sources
Vascular Ring: Right Aortic Arch, Mirror Image Branching with Kommerell's Diverticulum
Heart, Lung and Circulation, 2010Images of vascular ring-right aortic arch, mirror image branching with Kommerell's diverticulum and a brief comment on its management.
Krishnan Ganapathy, Subramaniam +1 more
openaire +2 more sources
Prenatal diagnosis of right aortic arch with mirror‐image branching without associated anomalies
Journal of Obstetrics and Gynaecology Research, 2013AbstractA pregnant woman at 32 weeks of gestation was referred because of untypical visualization of a three‐vessel tracheal view. Detailed ultrasound examination demonstrated an abnormal position of descending aorta, positioned at the right‐front side of the spine at the level of four‐chamber view.
Masahiko, Nakata +4 more
openaire +2 more sources
Annals of Nuclear Medicine, 2003
A 53-year-old male patient with a previous diagnosis of situs inversus with mirror-image dextrocardia underwent thallium-201 (Tl-201) stress-redistribution myocardial perfusion single photon emission computed tomography (SPECT). Electrocardiogram (ECG) obtained on right hemithorax revealed constant complete left bundle branch block.
Turgut, B +4 more
openaire +5 more sources
A 53-year-old male patient with a previous diagnosis of situs inversus with mirror-image dextrocardia underwent thallium-201 (Tl-201) stress-redistribution myocardial perfusion single photon emission computed tomography (SPECT). Electrocardiogram (ECG) obtained on right hemithorax revealed constant complete left bundle branch block.
Turgut, B +4 more
openaire +5 more sources
Right Aortic Arch with Mirror Image Branching and Situs Solitus: A case report on anatomic variation
The FASEB Journal, 2020During a routine cadaver dissection performed by first year medical students at Oakland University William Beaumont School of Medicine, a 60‐year‐old female cadaver was found to have right aortic arch with mirror image branching (RAMI). The descending aorta was observed to pass to the right of the midline and subsequently to cross left, anterior to the
Jordan L. Ensz +5 more
openaire +1 more source
Pediatric Cardiology, 2001
It is unusual to have a right aortic arch with mirror-image branching of the brachiocephalic vessels and no associated congenital cardiac anomalies. Pathogenetic factors of this anomaly, and associated development of the derivatives of the pharyngeal arches, have not been explored extensively.
D B, McElhinney +5 more
openaire +2 more sources
It is unusual to have a right aortic arch with mirror-image branching of the brachiocephalic vessels and no associated congenital cardiac anomalies. Pathogenetic factors of this anomaly, and associated development of the derivatives of the pharyngeal arches, have not been explored extensively.
D B, McElhinney +5 more
openaire +2 more sources