An unusual case of vascular ring: The right aortic arch with mirror-image branching and aneurysm of the left ductus arteriosus

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

2020 ◽  
Vol 41 (Supplement_2) ◽  
Author(s):  
G Amir ◽  
N Soffair ◽  
G Frenkel ◽  
E Bruckheimer ◽  
E Nachum ◽  
...  

Abstract Background Vascular anomalies of the Aortic arch can cause respiratory symptoms in children due to tracheal compression. Treatment consists of division of the vascular rings, nevertheless data regarding mid- term results is scarce. The purpose of this study was to evaluate clinical results of vascular ring surgery. Methods Between2007–2014, 85 children underwent vascular ring surgery. 51 had Double Aortic Arch (DAA, 60%), 31 Right Arch with Aberrant Subclavian Artery (RAA & ALSA, 36.5%) and 3 had RAA, mirror image branching & left ductus arteriosus (3.5%). Mean age and weight at operation were 12.4±13months and 8.6±4.1 kg respectively. Mid-term follow-up included clinical follow up by a pulmonologist (38 patients, 44.7%) and a telephone questionnaire (71 patients, 83%) performed 57±25.7 months after surgery. Results In most patients, symptomatic relief occurred in less than 6 months (table 1). Mid –term follow up revealed that although most parents described a significant improvement in their child's respiratory symptoms (95%), a significant number of patients described some residual respiratory symptoms (table 2). We did not find any significant association between age at surgery (under 6 month), or vascular ring anatomy (DAA vs. RAA&ASA) and the presence of residual symptoms at follow up Conclusions Surgical division of vascular rings results in a significant clinical improvement within one year, nevertheless many patients remain symptomatic to some degree. We found no association between the age at surgery or anatomic variant to the presence of symptoms in mid- term follow up. Further evaluation whether a more aggressive surgical approach is warranted in order to decrease the incidence long-term symptoms. Funding Acknowledgement Type of funding source: None


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

1978 ◽  
Vol 1 (3) ◽  
pp. 147-149 ◽  
Author(s):  
R. L. Horst ◽  
E. A. Fisher ◽  
I. W. DuBrow ◽  
A. R. Hastreiter

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.


2011 ◽  
Vol 40 (5) ◽  
pp. 240-243
Author(s):  
Sadanari Sawaki ◽  
Yuichi Hirate ◽  
Shinichi Ashida ◽  
Akira Takanohashi ◽  
Kei Yagami ◽  
...  

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