Anomalous Origin of Pulmonary Artery From Aorta: Neonatal Autologous Aortopulmonary Reconstruction

2017 ◽  
Vol 8 (4) ◽  
pp. 502-506
Author(s):  
Alexander J. Eason ◽  
Brent Shafer ◽  
Kenneth A. Murdison ◽  
Anastasios C. Polimenakos

Anomalous origin of a branch pulmonary artery (PA) from the ascending aorta is rather rare within the spectrum of congenital cardiovascular anomalies. In the scarce subset of patients with anomalous origin of right PA (RPA) from the ascending aorta originating from the lateral aspect of the distal ascending aorta, early neonatal repair by employing native aortic tissue for RPA reconstruction combined with translocation of the aorta posteriorly to the RPA can be an alternative option in the surgical armamentarium.

2018 ◽  
pp. 253-254 ◽  
Author(s):  
Michael C. Mongé ◽  
Osama Eltayeb ◽  
Andrada R. Popescu ◽  
Carl L. Backer

2012 ◽  
Vol 15 (1) ◽  
pp. 86-92 ◽  
Author(s):  
P. Garg ◽  
S. Talwar ◽  
S. S. Kothari ◽  
A. Saxena ◽  
R. Juneja ◽  
...  

2019 ◽  
Vol 10 (3) ◽  
pp. 13-14
Author(s):  
Manohar B Kachare ◽  
◽  
Vijay C Nalpe ◽  
Ravi Raval ◽  
◽  
...  

1995 ◽  
Vol 18 (2) ◽  
pp. 118-121 ◽  
Author(s):  
Tae Kyoung Kim ◽  
Yeon Hyoen Choe ◽  
Hak Soo Kim ◽  
Jae Kon Ko ◽  
Young Tak Lee ◽  
...  

2002 ◽  
Vol 12 (2) ◽  
pp. 186-188 ◽  
Author(s):  
Mi-Jin Jung ◽  
Shi-Joon Yoo

We report a case of anomalous origin of the right pulmonary artery from the ascending aorta that was diagnosed by fetal ultrasound at 21 weeks of gestation. The clue to the diagnosis was present in the three-vessel view, this being one of the views that we use for fetal cardiac screening. The anomaly was corrected surgically at 11 days of age. We discuss the importance of prenatal diagnosis in the management of this rare anomaly.


Herz ◽  
2013 ◽  
Vol 40 (2) ◽  
pp. 311-313 ◽  
Author(s):  
J. He ◽  
H. Li ◽  
Y. Li ◽  
L. Gui ◽  
X. Mao

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