Aortopulmonary Window; Hemitruncus

Author(s):  
Inder D. Mehta ◽  
Prashob Porayette ◽  
Ramon Julio Rivera ◽  
Amulya Buddhavarapu ◽  
Christopher Mehta
2008 ◽  
Vol 4 (1) ◽  
Author(s):  
MR Hoque ◽  
MA Hossain ◽  
Z Rahman ◽  
SMG Saklayen

2021 ◽  
Vol 49 (1) ◽  
pp. 030006052098465
Author(s):  
Mingyue Cui ◽  
Binfeng Xia ◽  
Heru Wang ◽  
Haihui Liu ◽  
Xia Yin

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.


2011 ◽  
Vol 26 (3) ◽  
pp. 174-178
Author(s):  
Shaoping Chen ◽  
Xianxian Zhao ◽  
Dong Jiang ◽  
Yongwen Qin

2020 ◽  
Vol 29 (1) ◽  
pp. 38-41
Author(s):  
Mamatha Gowda ◽  
Monica Reddy ◽  
Devika Ramesh ◽  
Srivatsa Prasad

2015 ◽  
Vol 149 (3) ◽  
pp. e38-e39 ◽  
Author(s):  
María-Teresa González-López ◽  
Juan-Miguel Gil-Jaurena ◽  
José-Luis Zunzunegui-Martínez ◽  
Reyes Álvarez-García-Rovés

2015 ◽  
Vol 30 (11) ◽  
pp. 846-848 ◽  
Author(s):  
Jiten Singh ◽  
Manpal Loona ◽  
Alok Suryavanshi ◽  
Manoranjan Sahoo ◽  
Tek S. Mahant

2012 ◽  
Vol 60 (03) ◽  
pp. 215-220 ◽  
Author(s):  
Peter Murin ◽  
Nicodème Sinzobahamvya ◽  
Hedwig Blaschczok ◽  
Joachim Photiadis ◽  
Christoph Haun ◽  
...  

2015 ◽  
Vol 99 (5) ◽  
pp. 1803-1805
Author(s):  
Brojendra N. Agarwala ◽  
Peter Varga ◽  
Ziyad M. Hijazi ◽  
Gerhard Ziemer

Author(s):  
Balaji Arvind ◽  
Velayoudam Devagourou ◽  
Anita Saxena

Aortopulmonary window (APW) seen in association with anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is extremely uncommon. When faced with this combination, ALCAPA usually goes undetected since most of the clinical and echocardiographic features of ALCAPA, including ventricular dysfunction are absent due to co-existent pulmonary hypertension. Herein we report a 5-month-old child with a large APW in whom a preoperative computed tomography angiogram facilitated the diagnosis of ALCAPA. The case is described for its rarity and the challenges faced during management. Also, it is extremely crucial that this coronary anomaly is identified and corrected during surgery, since failure to do so results in unforeseen postoperative ventricular dysfunction.


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