Pediatric Pulmonary Vascular Disease

Susan M. Dusenbery, Tal Geva, Anna Seale, Anne Marie Valente, Jing Zhou, Laureen Sena, Robert L. GeggelBoston Children’s Hospital.United States American Heart JournalAm Heart J 2013; 165: 770-777DOI: 10.1016/j.ahj.2013.01.016 AbstractBackground: Scimitar syndrome is a rare congenital anomaly. We evaluated risk factors for postoperative pulmonary vein stenosis or death and predictive factors for survival without scimitar vein surgery in patients with scimitar syndrome.Methods: The records of patients with scimitar syndrome

R. Aeba, T. Katogi, S. Takeuchi, S. KawadaKeio University.Japan Cardiovascular SurgeryCardiovasc Surg 1998; 6: 50-57DOI: 10.1016/s0967-2109(97)00112-9 AbstractSurgical treatment of the cardiac type of total anomalous pulmonary venous connection requires special techniques. The treatment and outcome in 17 consecutive patients who had undergone primary repairs of the cardiac type between 1965 and 1996 were reviewed. The median

Takahiko Sakamoto, Mitsugi Nagashima, Kentarou Umezu, Ryogo Houki, Jin Ikarashi, Junko Katagiri, Kenji YamazakiThe Heart Institute of Japan and Tokyo Women’s Medical University.Japan Interactive Cardiovascular and Thoracic SurgeryInteract Cardiovasc Thorac Surg 2018; 27: 20-26DOI: 10.1093/icvts/ivy034 AbstractObjectives: Isolated total anomalous pulmonary venous connection (TAPVC) is a relatively rare congenital cardiac defect, while pulmonary venous obstruction (PVO) is associated

Ko Bando, Mark W. Turrentine, Gregory J. Ensing, K. Sun, Thomas G. Sharp Y. Sekine, Donald A. Girod, John W. BrownJames W. Riley Hospital for Children.United States CirculationCirculation 1996; 94(9 Suppl): II12-II16DOI: Not Available AbstractBackground: Reports of surgical correction of total anomalous pulmonary venous connection (TAPVC) over the past 30 years indicate a general improvement in

Arkadi M. Rywlin, Rita M. FojacoUniversity of Miami.United States Pediatrics Pediatrics 1968; 41: 931–934https://doi.org/10.1542/peds.41.5.931 AbstractThree main theories have to be considered in the pathogenesis of congenital pulmonary lymphangectasis: obstruction of major pulmonary lymphatics, obstruction to pulmonary venous flow, and anomalous pulmonary development. The authors report an infant with congenital pulmonary lymphangiectasis associated with a blind common

Gary E. Gathman, Alexander S. NadasBoston Children’s Hospital and Harvard Medical SchoolUnited States CirculationCirculation 1970; 42: 143-154DOI: 10.1161/01.cir.42.1.143 SummaryExperience with 75 cases of proven total anomalous pulmonary venous connection without other significant cardiac malformations treated at the Children’s Hospital Medical Center in Boston from January 1950 to June 1968 forms the basis of this report. Clinical

Gita T. Mody, Gordan M. Folger, Jr.Henry Ford HospitalUnited States PediatricsPediatrics 1974; 54: 62-66DOI.org/10.1542/peds.54.1.62 AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary Hypertension Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article Access Free PDF File or Full Text Article Available

Alain Serraf, Emré Belli, Danie lRoux, Miguel Sousa-Uva, Francois Lacour-Gayet, Claude PlanchéMarie-Lannelongue Hospital.France Annals of Thoracic SurgeryAnn Thorac Surg 1998; 65: 1391-1393DOI: 10.1016/s0003-4975(98)00141-6 AbstractBackground: The main goal in the surgical repair of total anomalous pulmonary venous drainage is to reestablish a wide patent connection between the common pulmonary vein and the left atrium. Several techniques have been