Surgical repair of coronary sinus type partial anomalous pulmonary venous drainage with intact atrial septum

1998 ◽  
Vol 46 (11) ◽  
pp. 1211-1214 ◽  
Author(s):  
Atsushi Aoki ◽  
Takehiro Kubota ◽  
Mikizou Nakai ◽  
Masahiro Inoue ◽  
Syunji Sano
2010 ◽  
Vol 2010 ◽  
pp. 1-3
Author(s):  
Maryanne Caruana ◽  
Victor Grech ◽  
Jane Somerville

Hemianomalous pulmonary venous drainage with intact atrial septum is a rare congenital anomaly and reports of its surgical repair and the long-term complications related to the correction are only infrequently encountered in the literature. We report the case of a patient with hemianomalous pulmonary venous drainage and intact atrial septum who underwent surgical repair using a pericardial baffle and creation of an “atrial septal defect” aged 15 years. Dyspnoea and recurrent chest infections started 7 months after surgery when he was seen by a respiratory physician without cardiac followup. He presented again aged 28 years with a recurrent pneumonia investigated over 6 weeks and heart pronounced normal from examination and echocardiography. Correct diagnosis was made in Grown Up Congenital Heart (GUCH) clinic stimulating review of data and catheterisation with pulmonary artery angiography which confirmed it. We feel that this case highlights the importance of specialist care and followup for GUCH patients.


2016 ◽  
Vol 43 (5) ◽  
pp. 430-432
Author(s):  
Deepa Prasad ◽  
James P. Strainic ◽  
Khyati Pandya ◽  
Peter C. Kouretas ◽  
Ravi C. Ashwath

We report a rare causal association between obstructed supracardiac totally anomalous pulmonary venous drainage and coronary sinus ostial atresia. Our 12-week-old patient developed venous myocardial infarction secondary to coronary venous hypertension because her sole route of coronary venous drainage was obstructed. She recovered after the obstruction was relieved by balloon dilation. Surgical repair then included anastomosis of the pulmonary venous confluence to the left atrium, ligation of the vertical vein, and unroofing of the coronary sinus. Coronary sinus ostial atresia is rarely diagnosed before autopsy.


PEDIATRICS ◽  
1991 ◽  
Vol 87 (4) ◽  
pp. 584-584
Author(s):  
JACQUELINE A. NOONAN

To the Editor.— In a recent report, Moore et al1 reported that 3 of 12 patients with karyotype XO had partial anomalous pulmonary venous return with an intact atrial septum. In 1984, I presented a poster at the Southern Genetics Meeting which reported three patients with Turner syndrome who had partial anomalous pulmonary venous return demonstrated by cardiac catheterization. An additional infant with aortic atresia was noted at postmortem to have premature closure of the foramen ovale and partial anomalous pulmonary venous return.


2012 ◽  
Vol 1 (1) ◽  
pp. 33 ◽  
Author(s):  
Maryam Esmaeilzadeh ◽  
Mohammadtaghi Salehi-Omran ◽  
Saeid Hosseini ◽  
Mohammadali Sadr-Ameli

1980 ◽  
Vol 6 (3) ◽  
pp. 247-254 ◽  
Author(s):  
Arthur S. Pickoff ◽  
Rafael Sequeira ◽  
Pedro L. Ferrer ◽  
Dolores Tamer ◽  
Vicki Bennett ◽  
...  

2007 ◽  
Vol 17 (5) ◽  
pp. 554-556
Author(s):  
Masahiro Koh ◽  
Hideki Uemura ◽  
Koji Kagisaki

AbstractPartially anomalous pulmonary venous connection of a solitary pulmonary vein in the setting of an intact atrial septum is often subclinical, and the indications for surgical repair are controversial. Here we describe a patient who developed a significant shunt over a period of 10-years. Flow through the anomalously connected pulmonary segment depends on the difference of pressure between the right and left atrium, and may increase with age.


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