A Case of the Right Aortic Arch with Mirror-image Branching and a Left Ligamentum Arteriosum Forming a Vascular Ring

1998 ◽  
Vol 11 (1) ◽  
pp. 177
Author(s):  
Byung Pil Cho ◽  
Ho Suck Kang ◽  
Young Chul Yang ◽  
Tae Sun Hwang ◽  
Ji Won Kim
1973 ◽  
Vol 46 (542) ◽  
pp. 115-119 ◽  
Author(s):  
Izchak J. Garti ◽  
Maurice M. Aygen ◽  
Bernardo Vidne ◽  
Morris J. Levy

1995 ◽  
Vol 25 (6) ◽  
pp. 455-457 ◽  
Author(s):  
A. E. Schlesinger ◽  
E. Mendeloff ◽  
A. M. Sharkey ◽  
T. L. Spray

2014 ◽  
Vol 12 (3) ◽  
pp. 175-178
Author(s):  
Ali Yıldırım ◽  
Pelin Köşger ◽  
Gökmen Özdemir ◽  
Tevfik Demir ◽  
Birsen Uçar ◽  
...  

1990 ◽  
Vol 9 (1) ◽  
pp. 41-43
Author(s):  
H. Arakawa ◽  
K. Tokuyama ◽  
H. Mochizuki ◽  
M. Shigeta ◽  
M. Tashiro ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Silke Hecht ◽  
April M. Durant ◽  
William H. Adams ◽  
Gordon A. Conklin

A 4-month-old female mixed breed dog was presented to the University of Tennessee College of Veterinary Medicine with a history of regurgitation and cachexia. Thoracic radiographs revealed focal megaesophagus cranial to the heart base. Magnetic resonance imaging (MRI) was performed. True fast imaging with steady-state precession (TrueFISP), fast low angle shot (FLASH), and short tau inversion recovery (STIR) sequences were acquired prior to contrast medium administration. Contrast-enhanced magnetic resonance angiography (CE-MRA) demonstrated focal megaesophagus and position of the aortic arch to the right of the esophagus. A small ductus diverticulum and an indistinct linear soft tissue band crossing the esophagus were also noted. Surgical exploration confirmed MR diagnosis of a persistent right aortic arch (PRAA) with left ligamentum arteriosum. The dog improved following surgery but was unable to be transitioned to dry food. To our knowledge this is the first report describing the use of CE-MRA for preoperative diagnosis and guided surgical treatment of a vascular ring anomaly in a dog.


2020 ◽  
Vol 30 (6) ◽  
pp. 892-893
Author(s):  
Toyohide Endo ◽  
Daigo Ochiai ◽  
Mamoru Tanaka

AbstractThe right aortic arch is a congenital vascular anomaly, which may form a vascular ring. However, prenatal identification of the branching pattern of brachiocephalic vessels is often limited. In this paper, we clearly demonstrated the branching pattern of brachiocephalic vessels in a case of right aortic arch with an aberrant left subclavian artery using HDlive Flow imaging.


1985 ◽  
Vol 8 (3) ◽  
pp. 134-136 ◽  
Author(s):  
Vincent J. D'Souza ◽  
Guillermo Velasquez ◽  
Ted A. Glass ◽  
Augustin G. Formanek

2008 ◽  
Vol 130 (1) ◽  
pp. e53-e55 ◽  
Author(s):  
Yasutomi Higashikuni ◽  
Tamon Nagashima ◽  
Nobukazu Ishizaka ◽  
Koichiro Kinugawa ◽  
Yasunobu Hirata ◽  
...  

2021 ◽  
pp. 1-3
Author(s):  
Kei Kobayashi ◽  
Gen Harada ◽  
Takeshi Shinkawa

Abstract Right aortic arch in association with coarctation of the aorta and vascular ring is a rare anatomy. We present an infant with chromosome 22q11.2 deletion, who had the right aortic arch with retroesophageal aberrant left subclavian artery and left internal carotid artery. The left external carotid artery and right common carotid artery originated together from the ascending aorta as a bovine branch. The infant also had severe coarctation, which was prostaglandin dependent.


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