Extremely tortuous vertical vein in supracardiac totally anomalous pulmonary venous connection

Author(s):  
Mansi Verma ◽  
Niraj Nirmal Pandey ◽  
Balaji Arvind ◽  
Sanjeev Kumar
KYAMC Journal ◽  
2019 ◽  
Vol 10 (2) ◽  
pp. 118-121
Author(s):  
ASM Shariful Islam ◽  
Md Lutfar Rahman ◽  
Jayanta Kumar Saha ◽  
Mohammad Arifur Rahman ◽  
Mezanur Rahman ◽  
...  

Total anomalous pulmonary venous connection (TAPVC) is a rare congenital heart disease in which there is developmental absence of connection of all four pulmonary veins with the left atrium. To report a rare case and share our experience in surgery and post-operative management for supracardiac TAPVC. Patient with supracardiac TAPVC with atrial septal defect (ASD) secundum variety with rudimentary patent ductus arteriosus (PDA) underwent rechanneling of pulmonary veins to left atrium (LA) with gluteryldehye treated autologous pericardial patch closure of ASD with ligation of ascending vertical vein and ligation of rudimentary PDA.Post operatively there were no events of pulmonary hypertensive crisis, low cardiac output syndrome, right heart failure or conduction defect were observed and echocardiogram showed adequate pulmonary venous drainage with no residual shunt across the interatrial septum. Marked development in surgical results of TAPVC has been observed in recent years with declining mortality rate from 65% in early sixties to 5% in current surgical scenerio. KYAMC Journal Vol. 10, No.-2, July 2019, Page 118-121


2020 ◽  
Vol 2020 (10) ◽  
Author(s):  
Georgia R Layton ◽  
Marinos Koulouroudias ◽  
Eyad Issa ◽  
Steve Jepson ◽  
Antonio F Corno ◽  
...  

Abstract A 28-year-old male with infra-cardiac totally anomalous pulmonary venous connection (TAPVC) repaired as new-born presented in adulthood with right heart strain and very large left atrium to portal vein vessel. Residual connections from pulmonary veins to systemic circulation are believed to represent persistent ‘vertical veins’ (VV) not ligated at the time of the initial surgery. In our patient, since endovascular occlusion was not judged suitable, the anomalous vessel was surgically ligated and resected. A review of the literature failed to find such a procedure reported in an adult patient and analyzed the intra-operative ligation of VV during repair of TAPVC.


2001 ◽  
Vol 122 (3) ◽  
pp. 615-617 ◽  
Author(s):  
Raghavan Nair Suresh Kumar ◽  
Anil Kumar Dharmapuram ◽  
Ivatury M. Rao ◽  
Venkitachalam C. Gopalakrishnan ◽  
Velayudhan Ramakrishna Pillai ◽  
...  

1997 ◽  
Vol 64 (1) ◽  
pp. 23-29 ◽  
Author(s):  
Jeffrey T Cope ◽  
David Banks ◽  
Nancy L McDaniel ◽  
Kimberly S Shockey ◽  
Stanton P Nolan ◽  
...  

2017 ◽  
Vol 3 (6) ◽  
pp. 176-179 ◽  
Author(s):  
András Bratincsák ◽  
Elisa Rhee ◽  
William Van Alstine ◽  
Lindsay Koren ◽  
Kimberly Stoughton ◽  
...  

2012 ◽  
Vol 3 (4) ◽  
pp. 521-524 ◽  
Author(s):  
Sachin Talwar ◽  
Palleti Rajashekar ◽  
Robert H. Anderson ◽  
Priya Jagia ◽  
Neeti Makhija ◽  
...  

2009 ◽  
Vol 30 (7) ◽  
pp. 1043-1045
Author(s):  
Sejal Shah ◽  
Mukesh Singh ◽  
Colin John ◽  
Sunita Maheshwari

2007 ◽  
Vol 17 (5) ◽  
pp. 551-553 ◽  
Author(s):  
Aamir Jeewa ◽  
Gurdeep S. Mann ◽  
Martin C.K. Hosking

AbstractWe describe a combination, unique as far as we are aware, of tetralogy of Fallot with so-called “absent” pulmonary valve and supracardiac totally anomalous pulmonary venous connection. The vertical vein was obstructed in a neonate born at term who presented with respiratory compromise.


2012 ◽  
Vol 5 (2) ◽  
pp. 188
Author(s):  
Rajnish Juneja ◽  
SaurabhKumar Gupta ◽  
GurpreetSingh Gulati ◽  
Velayoudam Devagourou

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