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

[Proceedings: Ventricular septal defect associated with unilateral pulmonary vein stenosis and pulmonary hypertension]

K. Kinoshita, Y. Yamazaki, M. Kusakawa, K. Aoki, K. Yoshizumi Institution Not AvailablleJapan Japanese Circulation JournalJap Circ J 1975; 39: 874DOI: Not Available AbstractAbstract Not Available CategoryStenosis or Obstruction of Normal Pulmonary Venous Connections Year of Publication: 1975 Age Focus: Pediatric Article Type: Case Reports or Retrospective Observations in Small Groups of Patients (≤10 patients) […]

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The significance of lung scintigraphy in anomalies of the pulmonary vascular bed

C. Ruth, J. Skovránek, and Milan Samánek University Hospital MotoJCzechoslovakia Pediatric RadiologyPediatr Radiol 1975; 4: 21-27DOI: 10.1007/BF00978815 AbstractAplasia, hypoplasia and stenosis of the pulmonary artery showed, on scintigraphic investigation, unilateral, homogenous decreased in lung perfusion. In 3 of 4 children with pulmonary sequestration there was a difference in blood flow between the two lungs, or in

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Congenital unilateral pulmonary venous atresia with pulmonary veno-occlusive disease in contralateral lung: an unusual association

Savitri Shrivastava, James H . Moller, Jesse E . Edwards University of Minnesota.United States Pediatric CardiologyPediatr Cardiol 1986; 7: 213-219DOI: 10.1007/BF02093183 AbstractA patient presenting with the rare association of congenital unilateral pulmonary venous atresia in one lung and pulmonary veno-occlusive disease in the other is described. The patient first presented at the age of 3 1/2

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Unilateral pulmonary vein stenosis

John M. Reid, Morgan P. G. Jamieson, Michael D. Cowan Western Infirmary.United Kingdom British Heart JournalBrit Heart J 1986; 55: 599-601DOI: 10.1136/hrt.55.6.599 AbstractUnilateral pulmonary vein stenosis is a rare congenital anomaly. A case is described in a girl who first presented at the age of four years with recurring haemoptysis but in whom diagnosis was not

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Extreme dyspnea from unilateral pulmonary venous obstruction. Demonstration of a vagal mechanism and relief by right vagotomy

Scott F. Davies, Kenneth R. McQuaid, Conrad Iber, Charles McArthur, Michael Path, David S. Beebe, Hovald K. Helseth University of MinnesotaUnited States American Review of Respiratory DiseaseAm Rev Respir Dis 1987; 136: 184-188DOI: 10.1164/ajrccm/136.1.184 AbstractA 43-yr-old woman developed severe exertional dyspnea after an unsuccessful attempt to correct a total right anomalous pulmonary venous connection. A clotted

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Horseshoe lung with left lung hypoplasia and critical pulmonary venous stenosis

Joel Lutterman, Roy Jedeikin, David C. Cleveland Arizona Pediatric Cardiology Consultants.United States Annals of Thoracic SurgeryAnn Thorac Surg 2004; 77: 1085-1087DOI: 10.1016/S0003-4975(03)01213-X AbstractHorseshoe lung is a rare congenital anomaly characterized by an isthmus of the pulmonary parenchyma that extends posterior to the pericardial reflection at the cardiac apex and across the midline. There is unilateral, usually

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Anomalous unilateral single pulmonary vein: two cases mimicking arteriovenous malformations and a review of the literature

J. M. Hanson, A. M. Wood, R. Seymour, I.S. Petheram University Hospital, Cardiff.United Kingdom Australasian RadiologyAustralas Radiol 2005; 49: 246–251DOI: 10.1111/j.1440-1673.2005.01423.x AbstractTotal anomalous pulmonary venous drainage is a rare congenital anomaly. It usually involves a pulmonary to systemic venous shunt and most cases have a septal defect in order to survive. Anomalous pulmonary venous drainage with

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Supracardiac anomalous pulmonary venous connection with unilateral pulmonary venous atresia: Diagnosis and management

Vishal P. Changela, Suresh Pujar, Sunita Maheshwari Narayan Hrudayalaya Institute of Cardiac Sciences.India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2009; 2: 153-155DOI: 10.4103/0974-2069.58318 AbstractWe report a case of a 6-day-old neonate referred to us for surgical correction of total anomalous pulmonary venous connection. Meticulous evaluation contributed to accurate diagnosis of associated unilateral pulmonary venous atresia. This

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Isolated unilateral pulmonary vein atesia in adults

M. Teresa Gómez Hernández, María Rodríguez Pérez, Marcelo F. Jiménez Hospital Universitario de Salamanca.Spain Archivos de BronconeumologíaArch Bronconeumonol 2015; 51: 424-425DOI: 10.1016/j.arbres.2014.10.004 AbstractAbstract Not Available CategoryAbsence or Atresia of Normal Pulmonary Venous ConnectionsSymptoms and Quality of Life Associated with Pulmonary Venous ObstructionLength of Life Associated with Pulmonary Venous ObstructionDiagnostic Testing. Invasive Year of Publication: 2015 Age Focus: Adult

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[Unilateral congenital atresia in adults. A case report and review of the literature]

Juan Santos-Morano, Silvia Rodríguez-Hernández, Jesica Ivana Hilares-Vera Hospital de Valme.Spain Archivos de BronconeumologíaArch Bronconeumonol 2015; 51: 423-424DOI: 10.1016/j.arbres.2014.10.002 AbstractAbstract Not Available CategoryAbsence or Atresia of Normal Pulmonary Venous ConnectionsSymptoms and Quality of Life Associated with Pulmonary Venous Obstruction Length of Life Associated with Pulmonary Venous ObstructionDiagnostic Testing. Noninvasive Year of Publication: 2015 Age Focus: Adult Article

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