Type A interrupted aortic arch and type III aortopulmonary window with anomalous origin of the right pulmonary artery from the aorta

2018 ◽  
Vol 33 (6) ◽  
pp. 344-347 ◽  
Author(s):  
Ziyad M. Binsalamah ◽  
Christopher E. Greenleaf ◽  
Jeffrey S. Heinle
Keyword(s):  
Pulmonary Artery ◽  
Aortic Arch ◽  
Type A ◽  
Interrupted Aortic Arch ◽  
Anomalous Origin ◽  
Aortopulmonary Window ◽  
Type Iii ◽  
Right Pulmonary Artery ◽  
The Right

scholarly journals A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome

2021 ◽  
Vol 49 (1) ◽  
pp. 030006052098465
Author(s):  
Mingyue Cui ◽  
Binfeng Xia ◽  
Heru Wang ◽  
Haihui Liu ◽  
Xia Yin
Keyword(s):  
Pulmonary Artery ◽  
Rare Case ◽  
Congenital Heart ◽  
Respiratory Tract Infections ◽  
Anomalous Origin ◽  
Aortopulmonary Window ◽  
Eisenmenger Syndrome ◽  
Right Pulmonary Artery ◽  
The Right ◽  
Tract Infections

Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta, with Eisenmenger syndrome and without surgery.

Sign in / Sign up

Export Citation Format

Share Document