Total anomalous pulmonary venous connection

ESC CardioMed ◽  
2018 ◽  
pp. 831-834
Author(s):  
Marietta Charakida ◽  
John Deanfield

Total anomalous pulmonary venous connection is repaired in childhood and the long-term results are usually excellent. Recent surgical advances have reduced further the rate of recurrent pulmonary venous obstruction.

2002 ◽  
Vol 74 (5) ◽  
pp. 1616-1620 ◽  
Author(s):  
Paul M Kirshbom ◽  
Richard J Myung ◽  
J.William Gaynor ◽  
Richard F Ittenbach ◽  
Stephen M Paridon ◽  
...  

2006 ◽  
Vol 16 (5) ◽  
pp. 507-509 ◽  
Author(s):  
Kenji Waki ◽  
Yoshio Arakaki ◽  
Kiyoshi Baba

We report a 3-month-old female infant, in whom pulmonary venous obstruction occurred after repair of totally anomalous pulmonary venous connection, and which was successfully released by a transcatheter implantation of a stent using the transseptal approach. Close follow-up is required, since the long-term outcome is still unclear. Nevertheless, transcatheter implantation of stents is a promising option for treating this challenging lesion.


Circulation ◽  
1962 ◽  
Vol 25 (6) ◽  
pp. 916-928 ◽  
Author(s):  
ALOIS R. HASTREITER ◽  
MILTON H. PAUL ◽  
MARIAN E. MOLTHAN ◽  
ROBERT A. MILLER

1970 ◽  
Vol 25 (1) ◽  
pp. 98
Author(s):  
Manuel M.R. Gomes ◽  
Robert H. Feldt ◽  
Dwight C. McGoon ◽  
Gordon K. Danielson

1998 ◽  
Vol 46 (11) ◽  
pp. 1126-1132
Author(s):  
Katsunori Yoshihara ◽  
Tsukasa Ozawa ◽  
Hiroshi Sakuragawa ◽  
Takeshirou Fujii ◽  
Noritsugu Shiono ◽  
...  

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Takahiro Ito ◽  
Ikuo Hagino ◽  
Mitsuru Aoki ◽  
Kentaro Umezu ◽  
Tomohiro Saito ◽  
...  

Abstract Background Total anomalous pulmonary venous connection accompanied by unilateral lung agenesis and Goldenhar syndrome is extremely rare. Case presentation We present a case of total anomalous pulmonary venous connection accompanied by unilateral lung agenesis and Goldenhar syndrome in a patient who was diagnosed based on transthoracic echocardiography and computed tomography. We observed complete absence of the lung, the bronchial tree, and vascular structures on the right side, with abnormal drainage of the left pulmonary veins into the innominate vein. The patient showed clear clinical evidence of pulmonary venous obstruction and underwent surgery 3 days after birth. The pulmonary venous chamber containing the vertical vein was anastomosed to the left atrium using 7–0 PDS running sutures via a median sternotomy. Echocardiography and computed tomography performed 1 year postoperatively revealed no pulmonary venous obstruction. Conclusion We report a rare case of total anomalous pulmonary venous connection accompanied by unilateral lung agenesis and Goldenhar syndrome, which was successfully repaired 3 days after birth. A median sternotomy is a safe and effective approach for surgical repair of congenital heart disease with unilateral lung agenesis. Repair of the supra cardiac total anomalous pulmonary connection using the vertical vein is feasible in patients with a small pulmonary venous chamber.


2012 ◽  
Vol 94 (3) ◽  
pp. 825-832 ◽  
Author(s):  
S. Adil Husain ◽  
Elaine Maldonado ◽  
Debbie Rasch ◽  
Joel Michalek ◽  
Richard Taylor ◽  
...  

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