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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 CategoryAbsence or Atresia of Normal Pulmonary Venous Connections Year of Publication: 1974 Age Focus: Pediatric Article Type: Case Reports or Retrospective Observations in Small Groups of Patients (≤10 patients) Article Access: Free PDF File or Full Text […]

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Congenital pulmonary lymphangiectasis associated with a blind common pulmonary vein

Arkadi M. Rywlin, Rita M. Fojaco University 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

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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. Brown James 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

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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 Yamazaki The 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

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Correction of total anomalous pulmonary venous connection of the cardiac type

R. Aeba, T. Katogi, S. Takeuchi, S. Kawada Keio 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

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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. Geggel Boston 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

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

Donald Emslie-Smith, Ian G. W. Hill, Kenneth G. Lowe University 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 CategoryStenosis or Obstruction of Normal Pulmonary Venous ConnectionsPulmonary Hypertension Associated with Stenosis or Atresia of Pulmonary VeinsPulmonary Venous Pathology Year of Publication: 1955 Age Focus: Pediatric Article Type: Case

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Unilateral Pulmonary Arteriosclerosis Unusual Fibrous Connective Tissue Growth Associated; Review of Literature and Discussion of Possible Physiological Mechanisms Involved in These Changes

Scott R. Inkley, George R. Abbott Western Reserve University and University Hospitals of Cleveland.United States Journal of the American Medical Association Internal MedicineJAMA Int Med 1961; 108: 903-915https://doi:10.1001/archinte.1961.03620120087012 AbstractAn extensive fibrous connective tissue proliferation suggestive of retroperitoneal fibrosis or chronic mediastinitis is reported here. Aside from being the most extensive involvement that we can find

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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. Edwards Mayo ClinicUnited States American Medical Association Archives of PathologyAMA Arch Pathol 1955; 59: 463-470DOI: Not Available AbstractAbstract Not Available CategoryStenosis or Obstruction of Pulmonary Veins: Other CategoriesStenosis of individual pulmonary veins associated with cor triatriatum before the era surgical interventionPulmonary Venous Pathology Year

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The Hamman-Rich syndrome in childhood; report of a case with unilateral pulmonary arterial and venous stenosis and atriovenous occlusion

Israel Diamond Children’s Hospital and University of Louisville School of MedicineUnited States PediatricsPediatrics 1958; 22: 279–288https://doi.org/10.1542/peds.22.2.279 AbstractThe Hamman-Rich syndrome is described in a 4-year-old Negro male. The clinical picture was that of persistent cough and progressive dyspnea beginning at 4 months of age. Diagnosis was made ante mortem by lung biopsy. The fibrotic process and

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