Segmental Pulmonary Venous Disease. Without a Focus on Pulmonary Hypertension

Anomalous connection of pulmonary veins with normal pulmonary venous drainage; report of case associated with pulmonary venous stenosis and cor triatriatum

Luis M. Becu, W. Newlon Tauxe, James W. Dushane, Jesse E. EdwardsMayo ClinicUnited States American Medical Association Archives of PathologyAMA Arch Pathol 1955; 59: 463-470DOI: Not Available 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 […]

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Unilateral membranous pulmonary venous occlusion, pulmonary hypertension, and patent ductus arteriosus

Donald Emslie-Smith, Ian G. W. Hill, Kenneth G. LoweUniversity of St. Andrews.United Kingdom British Heart Journal (Heart)Brit Heart J 1955; 17: 79-84DOI: 10.1136/hrt.17.1.79 AbstractNo Abstract Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionPulmonary Vascular Pathology Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication

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Outcome predictors and implications for management of scimitar syndrome

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

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Correction of total anomalous pulmonary venous connection of the cardiac type

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

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Long-term outcomes of total correction for isolated total anomalous pulmonary venous connection: lessons from 50-years’ experience

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

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Surgical management of total anomalous pulmonary venous connection. Thirty-year trends

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

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Congenital pulmonary lymphangiectasis associated with a blind common pulmonary vein

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

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Total anomalous pulmonary venous connection: clinical and physiologic observations of 75 pediatric patients

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

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Atresia of the common pulmonary vein: report of one case

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

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Modified superior approach for repair of supracardiac and mixed total anomalous pulmonary venous drainage

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

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