Fetal echocardiographic diagnosis of a triad with common embryological origins: Cervical aortic arch, retro‐aortic left innominate vein and coarctation of the aorta

2021 ◽  
Author(s):  
Prema Ramaswamy ◽  
Jamie K. Harrington
2021 ◽  
pp. 1-2
Author(s):  
Stephen T. Dalby ◽  
Joshua A. Daily ◽  
Lawrence E. Greiten

Abstract We report a case of a newborn infant with coarctation of the aorta and hypoplastic transverse aortic arch who was found to have a circumaortic double left innominate vein on echocardiography. This exceedingly rare finding was important for surgical planning and was confirmed during congenital heart surgery.


2004 ◽  
Vol 50 (1) ◽  
pp. 27
Author(s):  
Young Min Han ◽  
Ja Hong Gu ◽  
Gong Yong Jin ◽  
Hyo Sung Kwak ◽  
Gyung Ho Chung ◽  
...  

2006 ◽  
Vol 30 (4) ◽  
pp. 672-672 ◽  
Author(s):  
Yoshitsugu Nakamura ◽  
Kiyoharu Nakano ◽  
Hayao Nakatani

2005 ◽  
Vol 22 (1) ◽  
pp. 43-45 ◽  
Author(s):  
Srinivas Vengala ◽  
Navin C. Nanda ◽  
Maninder Singh Sidhu ◽  
Harvinder S. Dod ◽  
Gopal Agrawal ◽  
...  

2020 ◽  
Author(s):  
Hideki Sasaki ◽  
Takashi Harada ◽  
Hiroshi Ishitoya ◽  
Osamu Sasaki

Abstract BackgroundRetroaortic innominate vein is a rare anomaly. It has been reported in patients with congenital anomalies such as Tetralogy of Fallot or right aortic arch. However, isolated retroaortic innominate vein is quite rare.Case presentationA 63-year-old man was transferred to our institution because of Stanford type A acute aortic dissection. Incidentally, we noticed that the left innominate vein coursed under the aortic arch and was directed into the superior vena cava on computed tomography. We performed emergent hemiarch replacement. ConclusionsAttention must be paid to the cannulation site for venous uptake and the method of myocardial protection.


2006 ◽  
Vol 20 (2) ◽  
pp. 166-170 ◽  
Author(s):  
Masaki Hara ◽  
Yasunori Matsuzaki ◽  
Tetsuya Shimizu ◽  
Masaki Tomita ◽  
Takanori Ayabe ◽  
...  

2020 ◽  
Author(s):  
Hideki Sasaki ◽  
Takashi Harada ◽  
Hiroshi Ishitoya ◽  
Osamu Sasaki

Abstract BackgroundRetroaortic innominate vein is a rare anomaly. It has been reported in patients with congenital anomalies such as Tetralogy of Fallot or right aortic arch. However, isolated retroaortic innominate vein is quite rare.Case presentationA 63-year-old man was transferred to our institution because of Stanford type A acute aortic dissection. Incidentally, we noticed that the left innominate vein coursed under the aortic arch and was directed into the superior vena cava on computed tomography. We performed emergent hemiarch replacement. ConclusionsAttention must be paid to the cannulation site for venous uptake and the method of myocardial protection.


2019 ◽  
Vol 29 (8) ◽  
pp. 1091-1093
Author(s):  
Utkarsh Kohli

AbstractRetroaortic course of left innominate vein is a rare venous anomaly which is usually associated with CHD. Isolated retroaortic innominate vein is exceedingly rare with only a handful of reported cases. We report an otherwise healthy newborn with isolated retroaortic innominate vein and right aortic arch, a combination which has previously not been reported.


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