scholarly journals Use of autogenous aortic and main pulmonary artery flaps for repair of anomalous origin of the right pulmonary artery from the ascending aorta

1996 ◽  
Vol 111 (3) ◽  
pp. 675-676 ◽  
Author(s):  
Jacques A.M. van Son ◽  
Frank L. Hanley
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

2000 ◽  
Vol 29 (1) ◽  
pp. 25-28
Author(s):  
Toshihiro Funatsu ◽  
Hidefumi Kishimoto ◽  
Hiroaki Kawata ◽  
Takuya Miura ◽  
Takayoshi Ueno ◽  
...  

1965 ◽  
Vol 50 (5) ◽  
pp. 726-733 ◽  
Author(s):  
S. Frank Redo ◽  
Harry R. Foster ◽  
Mary Allen Engle ◽  
Kathryn H. Ehlers

Author(s):  
Nguyen L.T. Truong ◽  
Tran Q. Vinh ◽  
Nguyen T. Mai

Anomalous origin of the right pulmonary artery from the ascending aorta (AORPA), sometimes referred to as hemitruncus, is a rare malformation. We report a unique case of AORPA associated with Ebstein's anomaly and with congenital tracheal stenosis due to complete tracheal rings. The AORPA and tracheal stenosis were both successfully corrected in the neonatal period.


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