An uncommon cause of respiratory distress in infancy: Right aortic arch anomaly

2012 ◽  
Vol 2 (3) ◽  
pp. 191-193
Author(s):  
Mahmut Dogru ◽  
Tayfur Ginis ◽  
İlknur Bostanci
Keyword(s):  
Respiratory Distress ◽  
Aortic Arch ◽  
Right Aortic Arch ◽  
Aortic Arch Anomaly

Right aortic arch and isolated left innominate artery from a left sided patent ductus arteriosus: a very rare aortic arch anomaly

2009 ◽  
Vol 44 (4) ◽  
pp. e29-e31 ◽  
Author(s):  
Emmanuel Le Bret ◽  
Bertrand Leobon ◽  
François Roubertie ◽  
Anne Sigal-Cinqualbre ◽  
Bertrand Stos ◽  
...  
Keyword(s):  
Patent Ductus Arteriosus ◽  
Aortic Arch ◽  
Ductus Arteriosus ◽  
Innominate Artery ◽  
Right Aortic Arch ◽  
Aortic Arch Anomaly ◽  
Patent Ductus

Right Aortic Arch Anomaly Masqurading As Bronchial Asthma

2014 ◽  
Vol 3 (2) ◽  
pp. 122-125
Author(s):  
Burcu Karaboga ◽  
Ahmet Gokhan Arslan ◽  
Aykut Cilli
Keyword(s):  
Aortic Arch ◽  
Bronchial Asthma ◽  
Right Aortic Arch ◽  
Aortic Arch Anomaly

scholarly journals Agenesis of the left pulmonary artery accompanied by right aortic arch anomaly: CT angiography findings of a case

2011 ◽  
Vol 17 (2) ◽  
pp. 123-124 ◽  
Author(s):  
Bilal Battal ◽  
Bulent Karaman ◽  
Veysel Akgun ◽  
Ugur Bozlar ◽  
Fatih Ors
Keyword(s):  
Pulmonary Artery ◽  
Aortic Arch ◽  
Ct Angiography ◽  
Left Pulmonary Artery ◽  
Right Aortic Arch ◽  
Aortic Arch Anomaly

scholarly journals A case of right aortic arch with isolated left innominate artery and global cerebral white matter atrophy

2019 ◽  
Vol 29 (8) ◽  
pp. 1107-1109
Author(s):  
Edem Binka ◽  
Lisa R. Sun ◽  
Philippe Gailloud ◽  
Joanne S. Chiu
Keyword(s):  
White Matter ◽  
Aortic Arch ◽  
Innominate Artery ◽  
Right Aortic Arch ◽  
Cerebral White Matter ◽  
Rare Form ◽  
Aortic Arch Anomaly ◽  
Neonatal Diagnosis

AbstractA right aortic arch with an isolated left innominate artery is a rare form of aortic arch anomaly. We present a case of neonatal diagnosis of this anomaly with concerning findings of global cerebral white matter atrophy at 13 months of age.

TEVAR Procedure in a Patient with Descending Aortic Aneurysm Accompanying Right Aortic Arch Anomaly: Case Report

2013 ◽  
Vol 22 (1) ◽  
pp. 48-51
Author(s):  
Orhan BOZOĞLAN ◽  
Bülent MEŞE ◽  
Erdinç EROĞLU ◽  
Murat ARI ◽  
Kemalettin ERDEM ◽  
...  
Keyword(s):  
Case Report ◽  
Aortic Aneurysm ◽  
Aortic Arch ◽  
Right Aortic Arch ◽  
Aortic Arch Anomaly ◽  
Descending Aortic Aneurysm

Kommerell's diverticulum of retroesophageal aberrant brachiocephalic artery with right aortic arch in an adult

2021 ◽  
pp. 021849232110563
Author(s):  
Otohime Mori ◽  
Keiichi Fujiwara ◽  
Kosuke Yoshizawa ◽  
Toshi Maeda ◽  
Hisanori Sakazaki
Keyword(s):  
Aortic Arch ◽  
Right Aortic Arch ◽  
Anatomical Reconstruction ◽  
Left Internal Carotid Artery ◽  
Brachiocephalic Artery ◽  
Descending Aorta ◽  
Aortic Arch Anomaly ◽  
Artery Graft ◽  
Kommerell’S Diverticulum ◽  
Midline Sternotomy

A retroesophageal aberrant brachiocephalic artery is a very rare congenital aortic arch anomaly. We herein presented a 29-year-old man with right aortic arch, retroesophageal aberrant left brachiocephalic artery, left ligamentum arteriosus, and absent left internal carotid artery. Graft replacement of the descending aorta and anatomical reconstruction of left brachiocephalic artery was successfully performed using a midline sternotomy approach without blood transfusion. We discuss the surgical management for Kommerell's diverticulum.

Sign in / Sign up

Export Citation Format

Share Document