Pediatric Pulmonary Vascular Disease or Adult Pulmonary Vascular Disease

Update on Eisenmenger syndrome – Review of pathophysiology and recent progress in risk assessment and management

Ranjan Banerjee, Alexander R. OpotowskyCincinnati Children’s Hospital and University of Cincinnati College of MedicineUnited States International Journal of Cardiology Congenital Heart DiseaseInt J Cardiol Congenit Heart Dis 2024; DOI: 10.1016/j.ijcchd.2024.100520 AbstractLongstanding left-to-right shunting associated with congenital heart disease (CHD) can ultimately lead to pulmonary vascular remodeling, pulmonary arterial hypertension, and shunt reversal, the hallmark feature of […]

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Pulmonary venous infarction

Warren A. Williamson, Bruce S. Tronic, Nathan Levitan, David G. Webb-Johnson, David M. Shahian, F. Henry Ellis, Jr.Lahey Clinic Medical Center.United States ChestChest 1992; 102: 937-940DOI: 10.1378/chest.102.3.937 AbstractPulmonary venous infarction, although rare, can develop in patients with the various pathologic conditions outlined. The triad of cough, dyspnea, and hemoptysis should raise clinical suspicion. The venous phase

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[Congenital unilateral pulmonary vein atresia: imaging findings]

I. Artero Muñoz, F. Serrano Puche, M. I. Padín Marín, F. Serrano RamosHospital Regional Universitario Carlos Haya.Spain RagiologíaRadiología 2008; 50: 82-85DOI: 10.1016/s0033-8338(08)71934-9 AbstractCongenital unilateral pulmonary vein atresia is a very rare anomaly that generally presents during childhood or adolescence as recurrent episodes of pulmonary infections or hemoptysis. Its presentation in adults is highly exceptional. We describe

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CT angiography of mildly symptomatic, isolated, unilateral right pulmonary vein atresia

Mindaugas Mataciunas, Lina Gumbiene, Sigitas Cibiras, Virgilijus Tarutis, Algirdas E. TamosiunasVilnius University.Lithuania Pediatric RadiologyPediatr Radiol 2009; 39: 1087-1090DOI: 10.1007/s00247-009-1291-9 AbstractWe report a mildly symptomatic 12-year-old boy with a very rare congenital anomaly-isolated unilateral pulmonary vein atresia. Diagnosis was made using CT angiography and its role in diagnosis is discussed. CategorySegmental Pulmonary Venous Disease. Without a Focus

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Extracorporeal membrane oxygenation as bridge to transplant in severe pulmonary hypertension

Sophie Kruszona, Khalil Aburahma, Philipp Wand, Nunzio D. de Manna, Murat Avsar, Dmitry Bobylev, Carsten Müller, Julia Carlens, Alexander Weymann, Nicolas Schwerk, Tobias Welte, Bin Liu, Arjang Ruhparwar, Christian Kuehn, Jawad Salman, Mark Greer, Fabio IusHannover Medical School.Germany European Journal of Cardiothoracic SurgeryEur J Cardiothorac Surg 2024; DOI: 10.1093/ejcts/ezae420 AbstractObjectives: Severe pulmonary hypertension is the leading lung

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Bioinformatic Analysis and Molecular Docking Identify Isorhamnetin Is a Candidate Compound in the Treatment of Pulmonary Artery Hypertension

Chen Shao, Wei Xia, Yang LiuSecond People’s Hospital of Lianyungang. Qilu Medical University. China Anatolgy Journal of CardiologyAnatol J Cardiol 2024;DOI: 10.14744/AnatolJCardiol.2024.4723 AbstractBackground: The current study aims to identify the key pathways and potential therapeutic targets for pulmonary arterial hypertension (PAH) and to further evaluate the anti-PAH effects of isorhamnetin.Methods: The dataset of gene expression profiling for PAH

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Case report: A finding of PVOD and PAH in first degree relatives suggests shared heritable risk and overlapping features of both pulmonary vascular diseases

Roger Winters, Lindsay M. Forbes, Dunbar Ivy, Carlyne Cool, Bryan D. Park, Peter Hountras, David Badesch, Sue Gu, Edda Spiekerkoetter, Roham Zamanian, Stacey Leier Gluck, Todd M. BullUniversity of Colorado and University of Colorado Children’s Hospital. Stanford University.United States Respirology Case ReportsRespirol Case Rep 2024; 12: DOI: 10.1002/rcr2.70064 AbstractPulmonary veno-occlusive disease (PVOD) is a rare form

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Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia

Lauren A. Beslow, Helen Kim, Steven W. Hetts, Felix Ratjen, Marianne S. Clancy, James R. Gossage, Marie E. FaughnanChildren’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania. University of California San Francisco. Hospital for Sick Children and University of Toronto. Cure HHT Foundation. Augusta University. St. Michael’s Hospital.United States and

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Trends and patterns in pulmonary arterial hypertension-associated hospital admissions among methamphetamine users: a decade-long study

Amanda Husein, Jolie Boullion, Ismail Hossain, Diensn Xing, Tareq Ferdous Khan, Shenuarin Bhuiyan, Gopi K. Kolluru, Mostafizur Rahman Bhuiyan, Nicholas E. Goeders, Steven A. Conrad, John A. Vanchiere A. Wayne Orr, Christopher G. Kevil, Mohammad Alfrad Nobel BhuiyanLouisiana State University Health Sciences Center at Shreveport. Cleveland State University. Bangabandhu Sheikh Mujib Medical University. United States

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Increased BMP-Responsive Transcription Factors in Distinct Endothelial and Mesenchymal Cells in PAH

Abam Michael Andruska, Rodrigo Cantu Valadez, Kenzo Ichimura, Pauline Chu, Tianyi Zhang, Katharina Schimmel, Lingli Wang, Aiqin Cao, Michaela A. Aldred, Edda SpiekerkoetterStanford University. University of California Berkeley. Indiana University School of Medicine.United States American Journal of Respiratory and Critical MedicineAm J Respir Crit Care Med 2024; DOI: 10.1164/rccm.202405-1039LE AbstractAbstract Not Available CategoryVascular Cell Biology and

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