Segmental Pulmonary Venous Disease. Without a Focus on Pulmonary Hypertension

Pulmonary vein obstruction: an uncommon sequel to chronic fibrous mediastinitis

Irving L. Bindelglass, Sidney TrubowitzVeterans Administration Hospital, East Orange, New JerseyUnited States Annals of Internal MedicineAnn Int Med 1958; DOI: 10.7326/0003-4819-48-4-876 AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary Hypertension Age Focus: Adult Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article Access Free PDF […]

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Observations on Resistance to the Flow of Blood to and from the Lungs

Richmond L. Moore, Carl A. L. BingerHospital of The Rockefeller Institute for Medical ResearchUnited States Journal of Experimental MedicineJ Exp Med 1927; 45: 655-671DOI: 10.1084/jem.45.4.655 Abstract1. Embolism of pulmonary arterioles and capillaries produced by the intravenous injection of starch grains results in a dilatation of the pulmonary artery and the right chambers of the heart. This

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Constrictive pericarditis with obstruction of pulmonary veins

Walter Lawrence Jr, W. E. Adams, Donald E. CasselsUniversity of ChicagoUnited States Journal of Thoracic SurgeryJ Thorac Surg 1948; 17: 832-840DOI: Not Available AbstractAbstract Not 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

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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 DiamondChildren’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 arteriolosclerosis

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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. 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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