Pulmonary Arteriovenous Malformations

Longitudinal Assessment of Curaçao Criteria in Children with Hereditary Hemorrhagic Telangiectasia

Mordechai Pollak, Dvir Gatt, Michelle Shaw, Sheryl L. Hewko, Anthony Lamanna, Sara Santos, Felix RatjenHospital for Sick Children. Ruth Rappaport Children’s Hospital. Canada and Israel Journal of PediatricsJ Pediatr 2023; DOI: 10.1016/j.jpeds.2023.113665 AbstractObjective: To assess the utility of the Curaçao criteria by age over time in children with hereditary hemorrhagic telangiectasia (HHT).Study design: This was a single-center, retrospective […]

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A Congenital Portosystemic Shunt in a Child With Heterotaxy, Situs Inversus, Polysplenia, and Interrupted Inferior Vena Cava With Azygous Continuation

Victoria Carvajal, Saigopala Reddy, Vani Gopalareddy, Adrienne Bean, Gonzalo WallisLevine Children’s Hospital. University of North Carolina Chapel Hill Medical School. United States American College of Gastroenterology Case Reports JournalACG Case Rep J 2023; DOI: 10.14309/crj.0000000000001201 AbstractCongenital portosystemic shunts are rare vascular malformations in which portal venous blood from the intestines and spleen bypasses the liver and

A Congenital Portosystemic Shunt in a Child With Heterotaxy, Situs Inversus, Polysplenia, and Interrupted Inferior Vena Cava With Azygous Continuation Read More »

A catheter-based interventional strategy redirects hepatic vein flows after Fontan procedure in left isomerism to treat severe hypoxemia

Kothandam SivakumarMadras Medical Mission.India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2022; 15: 212-215DOI: 10.4103/apc.apc_80_21 AbstractPulmonary arteriovenous malformations after the Kawashima procedure causing severe hypoxemia are treated by Fontan surgery that redirects hepatic venous blood to the pulmonary circulation. Alignment of the hepatic venous conduit toward both pulmonary arteries is crucial for their regression. Persistent hypoxemia due

A catheter-based interventional strategy redirects hepatic vein flows after Fontan procedure in left isomerism to treat severe hypoxemia Read More »

Management of an asymptomatic pulmonary arteriovenous fistula diagnosed prenatally by detachable balloon embolization: a case report

Wenjuan Li, Pengjun Zhao, Sun Chen Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine.China European Heart Journal Case ReportsEur Heart J Case Rep 2025; DOI: 10.1093/ehjcr/ytaf038 AbstractBackground: Pulmonary arteriovenous fistulas (PAVFs) are abnormal vascular malformations that connect pulmonary arteries and pulmonary veins, resulting in a right-to-left shunt. This anatomical shunt leads to a decrease in

Management of an asymptomatic pulmonary arteriovenous fistula diagnosed prenatally by detachable balloon embolization: a case report Read More »

Acquired Pulmonary Arteriovenous Malformation in a Case of a Pediatric Adrenocortical Carcinoma

Rahat-Ul-AinChildren’s Hospital and Institute of Child Health.Pakistan Journal of the College of Physicians and Surgeons PakistanJ Coll Physicians Surg Pak 2021; 31: 119-120DOI: 10.29271/jcpsp.2021.01.119 AbstractAbstract Not Available CategoryPulmonary Arteriovenous Malformations Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article Access Free PDF File or Full Text

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Determination of the Cause for Persistent Hypoxemia by Transesophageal Echocardiography After a Fontan Completion

Madan Mohan Maddali, Eapen Thomas, Pranav Subbaraya Kandachar, Nishant Ram Arora, Salim Nasser Al-MaskariRoyal Hospital. Oman Journal of Cardiothoracic and Vascular AnesthesiaJ Cardiothorac Vasc Anesth 2021; 35: 3135-3138DOI: 10.1053/j.jvca.2021.01.054 AbstractAbstract Not Available CategoryPulmonary Arteriovenous MalformationsDiagnostic Testing for Pulmonary Vascular Disease. Invasive Testing Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than

Determination of the Cause for Persistent Hypoxemia by Transesophageal Echocardiography After a Fontan Completion Read More »

Increases in oxygen saturation following discharge from Fontan palliation – an indicator of resolution of pulmonary arteriovenous malformations?

Hannah Van Galder, Amy M. Schaal, Mingen Feng, Amy Y. Pan, Michele A. Frommelt, Salil Ginde, Andrew D. SpearmanMedical College of Wisconsin and Children’s Wisconsin. United States Cardiology in the YoungCardiol Young 2021; 31: 1807-1813DOI: 10.1017/S1047951121000913 AbstractBackground: Pulmonary arteriovenous malformations in single ventricle congenital heart disease are poorly understood. Previous studies investigating pulmonary arteriovenous malformations predominantly focus

Increases in oxygen saturation following discharge from Fontan palliation – an indicator of resolution of pulmonary arteriovenous malformations? Read More »

Arteriovenous Malformations-Current Understanding of the Pathogenesis with Implications for Treatment

Katharina Schimmel, Khadem Ali, Serena Y. Tan, Joyce Teng, Huy M. Do, Gary K. Steinberg, David A. Stevenson, Edda SpiekerkoetterStanford University. Lucile Packard Children’s Hospital. United States International Journal of Molecular SciencesInt J Mol Sci 2021; 22: DOI: 10.3390/ijms22169037 AbstractArteriovenous malformations are a vascular anomaly typically present at birth, characterized by an abnormal connection between an

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Konar-MF™: Versatile Utility Suggests Potential to Simplify Congenital Catheterization Laboratory Inventory

Navaneetha Sasikumar, Pranoti Toshniwal. Usha Mandikal Kondakarna Sastry, Shweta Bakhru, Jayaranganath Mahimarangaiah, Nageshwara Rao Koneti, Raman Krishna KumarAmrita Institute of Medical Sciences. Sri Jayadeva Institute of Cardiovascular Sciences and Research. Rainbow Children’s Hospital.India Pediatric CardiologyPediatr Cardiol 2025; DOI: 10.1007/s00246-025-03849-x AbstractKONAR-MF™ device is a novel, cone-shaped, medium profile, self-expanding, double-disk, nitinol occlusive device designed for the ventricular

Konar-MF™: Versatile Utility Suggests Potential to Simplify Congenital Catheterization Laboratory Inventory Read More »

Editorial on “Elective Thoracic Surgical Resections for Pulmonary Arteriovenous Malformations-A 16 Year Single-Center Experience”

Raghav MurthyMedical City Children’s HospitalUnited States Pulmonary CirculationPulm Circ 2025; 15: DOI: 10.1002/pul2.70073 AbstractAbstract Not Available CategoryPulmonary Arteriovenous MalformationsSurgical and Catheter-mediated Interventions for Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication Article Access Free PDF File or Full Text Article Available Through PubMed

Editorial on “Elective Thoracic Surgical Resections for Pulmonary Arteriovenous Malformations-A 16 Year Single-Center Experience” Read More »

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