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 Total anomalous pulmonary venous connection masking an aortopulmonary window: A rare combination of defects

Shyamajit Samaddar1, Dheeraj Bhatt1, Munish Guleria2, Dinesh Kumar Yadav1, Anubhav Gupta3
1 Department of Pediatrics, Division of Pediatric Cardiology, Dr RML Hospital and PGIMER, New Delhi, India
2 Department of Radiology, Dr RML Hospital and PGIMER, New Delhi, India
3 Department of CTVS, Dr RML Hospital and PGIMER, New Delhi, India

Correspondence Address:
Dr. Dheeraj Bhatt
Room No 238 (OPD Building), Department of Pediatrics, Division of Pediatric Cardiology, Dr RML Hospital and PGIMER, New Delhi - 110 001
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_45_18

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Year : 2018  |  Volume : 11  |  Issue : 3  |  Page : 322-324

 
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The association of aortopulmonary (AP) window with total anomalous pulmonary venous connection (TAPVC) has so far not been reported. We report a unique case of an 8-month-old child who presented with congestive cardiac failure and severe pulmonary arterial hypertension. Initial echocardiography revealed supracardiac TAPVC. Cardiac computed tomography showed the presence of Type I AP window along with the TAPVC. In the presence of severe pulmonary hypertension and dilated right ventricle, AP window may easily be missed if not actively looked for.






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 © 2008 Annals of Pediatric Cardiology | Published by Wolters Kluwer - Medknow
 Online since 20th April, 2008

 

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Shyamajit Samaddar1, Dheeraj Bhatt1, Munish Guleria2, Dinesh Kumar Yadav1, Anubhav Gupta3
1 Department of Pediatrics, Division of Pediatric Cardiology, Dr RML Hospital and PGIMER, New Delhi, India
2 Department of Radiology, Dr RML Hospital and PGIMER, New Delhi, India
3 Department of CTVS, Dr RML Hospital and PGIMER, New Delhi, India

Correspondence Address:
Dr. Dheeraj Bhatt
Room No 238 (OPD Building), Department of Pediatrics, Division of Pediatric Cardiology, Dr RML Hospital and PGIMER, New Delhi - 110 001
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_45_18

Rights and Permissions

The association of aortopulmonary (AP) window with total anomalous pulmonary venous connection (TAPVC) has so far not been reported. We report a unique case of an 8-month-old child who presented with congestive cardiac failure and severe pulmonary arterial hypertension. Initial echocardiography revealed supracardiac TAPVC. Cardiac computed tomography showed the presence of Type I AP window along with the TAPVC. In the presence of severe pulmonary hypertension and dilated right ventricle, AP window may easily be missed if not actively looked for.






[FULL TEXT] [PDF]*


        
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 © 2008 Annals of Pediatric Cardiology | Published by Wolters Kluwer - Medknow
 Online since 20th April, 2008