Esophageal duplication cyst and aberrant right subclavian artery mimicking a symptomatic vascular ring

1989 ◽  
Vol 19 (8) ◽  
pp. 543-544 ◽  
Author(s):  
G. L. Helund ◽  
G. S. Bisset
2013 ◽  
Vol 96 (1) ◽  
pp. e15-e16 ◽  
Author(s):  
Zhi-Jun Dai ◽  
Hua-Feng Kang ◽  
Shuai Lin ◽  
Ming-Hua Bai ◽  
Li Ma ◽  
...  

2021 ◽  
Author(s):  
A Taleb ◽  
N Roshdy ◽  
A Montasser ◽  
M Madbouly ◽  
M Ibrahim

2009 ◽  
Vol 19 (1) ◽  
pp. 75 ◽  
Author(s):  
Rangasami Rajeswaran ◽  
Anupama Chandrasekharan ◽  
Lal Archana ◽  
Joseph Santhosh

1987 ◽  
Vol 20 (8) ◽  
pp. 1952-1955 ◽  
Author(s):  
Hidekazu SADATSUKI ◽  
Michio KAMINISHI ◽  
Sigeru SAKAI ◽  
Hiromi SANO ◽  
Shouji KANEKO ◽  
...  

2017 ◽  
Vol 85 (5) ◽  
pp. AB114
Author(s):  
Paul Korc ◽  
Nikolai A. Bildzukewicz ◽  
John C. Lipham ◽  
Phuong T. Nguyen

2021 ◽  
Author(s):  
Xiaoming Bian

Diverticulum of Kommerell is a congenital anomaly in the development of the primitive embryonic aortic vasculature resulting in either an aberrant left subclavian artery (ALSA) from a right-sided aortic arch (RSAA) or an aberrant right subclavian artery (ARSA) from a left-sided aortic arch (LSAA). Kommerell’s diverticulum (KD), is extremely rare in the general population having prevalence of 0.7–2.0 %. KD with true aneurysmal dilatation like any vascular lesion of the thoracic aorta weakens the vasculature and increases the risk of aortic rupture. Timely surgical intervention is of paramount importance in most of these cases. Variable clinical presentations in patients with KD are either a result of compression of some mediastinal organs or strangulation by the vascular ring from the aberrant subclavian artery (ASA). We report a case of a 39 years old Chinese female with a rare co-existence of a huge KD with a microaneurysm, an aberrant right subclavian artery (ARSA), and ventricular septal defect (VSD). She underwent a successful operation and all her pre-surgical symptoms disappeared.


2021 ◽  
Author(s):  
Samantha Snyder ◽  
Mark T. DiMarcangelo, DO, MSc

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