Roberta M. Bini, David C. Cleveland, Ricardo Ceballos, Lionel M. Bargeron, Albert D. Pacifico, John W. Kirklin University of Alabama BirminghamUnited States American Journal of CardiologyAm J Cardiol 1984; 54: 369-375DOI: 10.1016/0002-9149(84)90199-1 AbstractCongenital pulmonary vein stenosis is a rare and serious form of congenital heart disease. Between 1969 and 1982 10 patients with this lesion were […]
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Lars Grosse-Wortmann, Abdulmajeed Al-Otay, Hyun Woo Goo, Christopher K. Macgowan, John G. Coles, Leland N. Benson, Andrew N. Redington, Shi-Joon Yoo Hospital for Sick Children and The University of Toronto.Canada Journal of the American College of CardiologyJ Am Coll Cardiol 2007; 49: 993-1002DOI: 10.1016/j.jacc.2006.09.052 AbstractPulmonary vein pathologies often present a diagnostic challenge. Among the different imaging
Mathias Emmel, I. Bauer, M. Plug, Sabine Schickendantz, U. Mennicken University of Cologne.Germany Pediatric CardiologyPediatr Cardiol 1997; 18: 306-308DOI: 10.1007/s002469900180 AbstractWe describe two cases of left-side pulmonary vein obstruction observed after the arterial switch operation (Jatene) for D-transposition of the great arteries. This appears to be related to left-sided pulmonary vein obstruction occurring coincidently with D-transposition
Michael Vogel, Judith Ash, Richard D. Rowe, George A. Trusler, Marlene Rabinovitch Hospital for Sick Children and University of Toronto.Canada American Journal of CardiologyAm J Cardiol 1984; 54: 166-171DOI:https://doi.org/10.1016/0002-9149(84)90323-0 AbstractFour patients with transposition of the great arteries and unilateral pulmonary vein (PV) stenosis, all left-sided, were studied. Two patients had an intact ventricular septum (1
Ankit Bharat, Deidre J. Epstein, Mark Grady, Albert Faro, Peter Michelson, Stuart C. Sweet, Charles B. Huddleston Washington University.United States Journal of Heart and Lung TransplantationJ Heart Lung Transplant 2013; 32: 621-625DOI: 10.1016/j.healun.2013.03.002 AbstractBackground: Congenital pulmonary vein stenosis (PVS) is associated with high mortality because surgical repair is usually not feasible or is ineffective. In addition, acquired
Hideshi Tomita, Satoshi Yazaki, Kohji Kimura, Ken Watanabe, Kinya Hatakeyama, Yasuo Ono, Shigeyuki Echigo National Cardiovascular Center.Japan Cardiology in the YoungCardiol Young 2003; 13: 519-525DOI: Not Available AbstractWe implanted either large or medium Palmaz stents, or a Palmaz Corinthian stent, in various stenotic vessels, such as the pulmonary arteries, pulmonary veins, aorta, or superior caval
Victoria Sokoliuk, James A. DiNardo, Morgan L. Brown Boston Children’s Hospital.United States A and A PracticeA A Pract 2019; 12: 205-207DOI: 10.1213/XAA.0000000000000885 AbstractPulmonary vein stenosis (PVS) is a progressive disease with pulmonary hypertension (PH) as a major cause of morbidity and mortality. Traditional management of PH with inhaled nitric oxide (iNO) is typically avoided in PVS
Michelle C. Sykes, Christina Ireland, Julia E. McSweeney, Emily Rosenholm, Kristofer G. Andren, Thomas J. Kulik Boston Children’s Hospital.United States Pulmonary CirculationPulm Circ 2018;DOI: 10.1177/2045894018776894 AbstractPulmonary vein stenosis (PVS) is associated with pulmonary hypertension (PH), but there is little information regarding the impact of PH on right ventricular (RV) systolic function and survival. We conducted a
Kevin S. Roman, Christian Kellenberger, Christopher K. Macgowan, John Coles, Andrew N. Redington, Lee N. Benson, Shi-Joon Yoo Hospital for Sick Children.Canada Pediatric RadiologyPediatr Radiol 2005; 35: 580-586DOI: 10.1007/s00247-004-1399-x AbstractBackground: Hemodynamic changes within a stenosed pulmonary vein might not reflect the severity of the obstruction if redistribution of pulmonary artery flow occurs.Objective: The purpose was to investigate flow
Gerald F. Greil, Andrew J. Powell, Hans P. Gildein, Tal Geva Children’s Hospital, Boston.United States Journal of the American College of CardiologyJ Am Coll Cardiol 2002; 39: 335-341DOI: 10.1016/s0735-1097(01)01730-2 AbstractObjective: The goal of this study was to evaluate the diagnostic value of gadolinium (Gd)-enhanced three-dimensional (3D) magnetic resonance angiography (MRA) in patients with congenital and acquired anomalies
