نتایج جستجو برای: aortic arch

تعداد نتایج: 126647  

Journal: :British heart journal 1982
S Milo C Massini D A Goor

Isolated atresia of the aortic arch is rare. In aortic arch atresia the arch is continuous, yet a segment of it is atretic so that apart from a collateral circulation, communication with the lower aortic segment is absent. Haemodynamically, the condition is similar to complete interruption of the aortic arch. To our knowledge only 10 cases of isolated aortic arch atresia or interruption have be...

Journal: :Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2003
S-J Yoo J-Y Min Y-H Lee K Roman E Jaeggi J Smallhorn

Aortic arch anomalies refer to congenital abnormalities of the position or branching pattern, or both of the aortic arch. Although aortic arch anomalies are not uncommon, reports on their prenatal diagnosis are scarce. Insight into the hypothetical arch model is crucial to understanding anomalies of the aortic arch in the fetus. Recognition of the trachea, three major vessels, ductus arteriosus...

Journal: :Journal of atherosclerosis and thrombosis 2010
Yuzuru Ito Koichiro Yoshimura Yoko Matsuzawa Jun Saito Hiroko Ito Hiroshi Furukawa Kazuhiro Okura Mutsumu Fukata Toshio Konishi Tetsuo Nishikawa

We describe a diabetic patient successfully treated for an acute mycotic aortic arch pseudoaneurysm with primary aldosteronism. The patient first complained of severe pain in the left upper extremity and left back with high C reactive protein (CRP) and high-grade fever. It was suspected that acute aortic dissection had developed in association with mycotic pseudoaneurysm of the aortic arch beca...

Journal: :Journal of the American College of Cardiology 1998
W T Mahle J Rychik P M Weinberg M S Cohen

OBJECTIVES We sought to characterize the growth of the reconstructed aortic arch after the Norwood operation (NO). BACKGROUND The first stage of surgical palliation of hypoplastic left heart syndrome (HLHS), the NO, includes augmentation of the aortic arch with homograft. Growth characteristics of the reconstructed aortic arch, which is comprised of both native aortic tissue and homograft, ha...

Journal: :Circulation 1992
L K Hornberger R G Weintraub E Pesonen A Murillo-Olivas I A Simpson C Sahn S Hagen-Ansert D J Sahn

BACKGROUND In a study of normal and abnormal growth of the aorta before birth, high-resolution echocardiographic imaging of the aortic arch in 92 normal fetuses aged 16-38 weeks was used to establish normal values for aortic arch dimensions at varying gestational ages. METHODS AND RESULTS From long-axis views of the aortic arch, the internal diameter of the aortic root, ascending aorta, trans...

2005
Lisa K. Hornberger Azucena Murillo-Olivas David J. Sahn

Background. In a study of normal and abnormal growth of the aorta before birth, high-resolution echocardiographic imaging of the aortic arch in 92 normal fetuses aged 16-38 weeks was used to establish normal values for aortic arch dimensions at varying gestational ages. Methods and Results. From long-axis views of the aortic arch, the internal diameter of the aortic root, ascending aorta, trans...

Journal: :International heart journal 2017
Qingwang Hua Zhiyong Lin Xingti Hu Qifeng Zhao

Congenital abnormalities of the aortic arch include interrupted aortic arch (IAA), coarctation of the aorta (CoA), and double aortic arch (DAA). Aortic arch repair is difficult and postoperative complications are common. However, postoperative tracheobronchial stenosis with respiratory insufficiency is an uncommon complication and is usually caused by increased aortic anastomotic tension. We re...

Journal: :Pediatrics 2003
Doff B McElhinney Deborah A Driscoll Elissa R Levin Abbas F Jawad Beverly S Emanuel Elizabeth Goldmuntz

BACKGROUND A ventricular septal defect (VSD) is the most common form of congenital heart disease and is one of the most common cardiovascular anomalies in individuals with chromosome 22q11 deletion syndrome. However, the frequency of a chromosome 22q11 deletion in patients with a VSD is not known. In addition, among patients with a VSD, it is not clear whether particular types of VSD or associa...

Journal: :Interactive CardioVascular and Thoracic Surgery 2010

Journal: :Journal of cancer research and therapeutics 2013
Arvind Krishnamurthy

CT revealed also a right aortic arch, classified as an aortic anomaly of type III-A: A mirror image branching of the normal left aortic arch, according to Edward’s classification (Panel B). Type IIIB is the most frequent, followed by Type IIIA. The classification of aortic anomalies by Edward’s et al. is based on their theoretical concept of the development of the aortic arch. Right aortic arch...

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