Article Type: Case Reports or Retrospective Observations in Small Groups of Patients (≤10 patients)

Pulmonary vein atresia with severe contralateral pulmonary vein stenosis in a child

Jeffrey E. Vergales, Shawn C. West, Andrew W. Hoyer University of Virginia Health SystemUnited States Pediatric CardiologyPediatr Cardiol 2012; 33: 663-665DOI: 10.1007/s00246-012-0178-y AbstractUnilateral pulmonary vein atresia is a very rare congenital anomaly associated with high morbidity and mortality. Most cases present in infancy or childhood with recurrent respiratory infections or hemoptysis. Further, the diagnosis can often

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Serum Levels After Everolimus-Stent Implantation and Paclitaxel-Balloon Angioplasty in an Infant with Recurrent Pulmonary Vein Obstruction After Repaired Total Anomalous Pulmonary Venous Connection

Matthias J. Muller, Ulrich Krause, Thomas Paul, Heike E. Schneider Georg-August-University Göttingen.Germany Pediatric CardiologyPediatr Cardiol 2011; 32: 1036-1039DOI: 10.1007/s00246-011-0054-1 AbstractEverolimus-eluting stents and paclitaxel-coated balloons are used in the interventional treatment of coronary artery disease in adults to reduce the restenosis rate and in small-vessel disease. Both substances are released into the circulation. We report systemic drug

Serum Levels After Everolimus-Stent Implantation and Paclitaxel-Balloon Angioplasty in an Infant with Recurrent Pulmonary Vein Obstruction After Repaired Total Anomalous Pulmonary Venous Connection Read More »

Cardiopulmonary magnetic resonance imaging in children after lung transplantation: preliminary observations

Lars Grosse-Wortmann, Shi-Joon Yoo, Melinda Solomon, Christopher K. Macgowan, Shaf Keshavjee, Hartmut Grasemann Hospital for Sick Children and University of Toronto.Canada Journal of Heart and Lung TransplantationJ Heart Lung Transplant 2011; 30: 1294-1298DOI: 10.1016/j.healun.2011.07.008 AbstractBackground: Lung transplantation carries a guarded prognosis and is burdened by short-term and long-term complications that affect the airway, lungs, and vasculature. In

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Hypoplastic right lung associated with right pulmonary vein stenosis and systemic collateral

Anant Khositseth, Suvipaporn Siriporpitak, Preecha Laohakunakorn Ramathibodi Hospital Mahidol University.Thailand Congenital Heart DiseaseCongenit Heart Dis 2010; 5: 76-80DOI: 10.1111/j.1747-0803.2009.00324.x AbstractWe present a case of a 6-month-old girl diagnosed as unilateral pulmonary vein stenosis (right inferior pulmonary vein) with dextroposition of the heart, hypoplastic right lung, hypoplastic right pulmonary artery, collateral from the descending aorta supplied right

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Role of left atrial hypertension in pulmonary hypertension associated with bronchopulmonary dysplasia

Rachel T. Sullivan, Megha D. Tandel, Shazia Bhombal, Gregory T. Adamson, Derek B. Boothroyd, Michael Tracy, Amanda Moy, Rachel K. Hopper Vanderbilt University Medical Center. Stanford University.United States Frontiers in PediatricsFront Pediatr 2022;DOI: 10.3389/fped.2022.1012136 AbstractLeft atrial hypertension (LAH) may contribute to pulmonary hypertension (PH) in premature infants with bronchopulmonary dysplasia (BPD). Primary causes of LAH in

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Treatment of pulmonary vein stenosis with expanded polytetrafluoroethylene covered stents

Brent M. Gordon, John W. Moore Rady Children’s Hospital and University of California, San Diego.United States Catheterization and Cardiovascular InterventionsCatheter Cardiovasc Interv 2010; 75: 263-267DOI: 10.1002/ccd.22240 AbstractAtrium expanded polytetrafluoroethylene covered stents were implanted in the stenotic pulmonary veins (n = 5) of three patients. Use of this device was feasible in infants and the procedure was

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Infantile form of scimitar syndrome with contralateral pulmonary vein stenosis

I. Ricardo Argueta-Morales, Lauren C. Meador, David G. Nykanen, William M. DeCampli Arnold Palmer Hospital for Children.United States Pediatric CardiologyPediatr Cardiol 2010; 31: 550-552DOI: 10.1007/s00246-009-9630-z AbstractInfantile scimitar syndrome (SS) carries significant mortality. Consistent management guidelines have not been well established, and outcomes continue to be disappointing. We present our experience managing an SS patient with complex

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First experience with a new drug-eluting balloon for the treatment of congenital pulmonary vein stenosis in a neonate

Goetz Christoph Mueller, Ali Dodge-Khatami, Jochen Weil University Heart Center Hamburg.Germany Cardiology in the YoungCardiol Young 2010; 20: 455-458DOI: 10.1017/S1047951110000703 AbstractPaclitaxel-eluting balloons are a new and innovative method in the treatment of in-stent stenosis and small vessel disease in adult cardiac pathology. The treatment of congenital pulmonary vein stenosis is difficult to manage, and results in

First experience with a new drug-eluting balloon for the treatment of congenital pulmonary vein stenosis in a neonate Read More »

Successful pediatric single-lung transplantation with previous contralateral pneumonectomy, using controlled “donation after cardiac death” lung, for congenital pulmonary vein stenosis

Amit Pawale, Michael McKean, John Dark, Asif Hasan Freeman Hospital.United Kingdom Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 2010; 139: e125-e126DOI: 10.1016/j.jtcvs.2009.06.006 AbstractAbstract Not Available CategoryStenosis or Obstruction of Normal Pulmonary Venous ConnectionsSymptoms and Quality of Life Associated with Pulmonary Venous ObstructionSurgical Interventions for Pulmonary Venous Obstruction After the Onset of Disease Lung Transplantation

Successful pediatric single-lung transplantation with previous contralateral pneumonectomy, using controlled “donation after cardiac death” lung, for congenital pulmonary vein stenosis Read More »

Results of intravascular stent placement for fibrosing mediastinitis

Matthew E. Ferguson, Allison K. Cabalka, Frank Cetta, Donald J. Hagler Mayo Clinic.United States Congenital Heart DiseaseCongenit Heart Dis 2010; 5: 124-133DOI: 10.1111/j.1747-0803.2010.00387.x AbstractObjective: Fibrosing mediastinitis is a rare disorder characterized by an excessive fibrotic reaction in the mediastinum which can result in compromise of mediastinal structures. We sought to evaluate short- and midterm results of intravascular

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