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

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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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

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

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

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

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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Constrictive pericarditis with obstruction of pulmonary veins

Walter Lawrence Jr, W. E. Adams, Donald E. Cassels University of ChicagoUnited States Journal of Thoracic SurgeryJ Thorac Surg 1948; 17: 832-840DOI: Not Available AbstractAbstract Not Available CategoryStenosis or Obstruction of Normal Pulmonary Venous ConnectionsPatient Factors Influencing the Onset, Severity or Outcome of DiseasePulmonary Venous Pathology Year of Publication: 1948 Age Focus: Pediatric Article Type:

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Multilobar pulmonary venous obstruction with pulmonary hypertension; protective arterial lesions in the involved lobes

Jesse E. Edwards, Howard B. Burchell Mayo ClinicUnited States American Medical Association Archives of Internal MedicineAMA Arch Intern Med 1951; 87: 372-378.DOI: 10.1001/archinte.1951.03810030045004 AbstractIn the presence of structural obstruction to the free flow of blood from the lungs to the left ventricle, such as in classic mitral stenosis, proliferative thickening of the walls of the small arteries

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Pulmonary vein obstruction: an uncommon sequel to chronic fibrous mediastinitis

Irving L. Bindelglass, Sidney Trubowitz Veterans 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 CategoryStenosis or Obstruction of Normal Pulmonary Venous ConnectionsPatient Factors Influencing the Onset, Severity or Outcome of DiseasePulmonary Venous Pathology Year of Publication: 1958 Age Focus: Adult Article Type: Case Reports or Retrospective

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Significance of the Pulmonary Vascular Bed in Congenital Heart Disease: V. Lesions of the Left Side of the Heart Causing Obstruction of the Pulmonary Venous Return

Charlotte Ferencz, J. Francis Dammann Johns Hopkins University and Hospital. University of Virginia.United States CirculationCirculation 1957; 16:1046-1056DOI: 10.1161/01.cir.16.6.1046 AbstractA microscopic study was made of the lungs of 18 patients with congenital malformations of the heart in which there was obstruction of pulmonary venous drainage. Alterations in various components of the pulmonary vascular bed and of the

Significance of the Pulmonary Vascular Bed in Congenital Heart Disease: V. Lesions of the Left Side of the Heart Causing Obstruction of the Pulmonary Venous Return Read More »

Stenosis and obstruction of the pulmonary veins associated with pulmonary artery hypertension

George Contis, Robert H. Fung, Gordon F. Vawter, Alexander Nadas The Children’s Hospital Medical Center and Harvard Medical School.United States American Journal of CardiologyAm J Cardiol 1967; 20: 718-724DOI: 10.1016/0002-9149(67)90015-x AbstractA case of stenosis and obstruction of the pulmonary veins associated with pulmonary artery hypertension and microcytic anemia, is presented. The child was completely normal until

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