Pulmonary Arteriovenous Malformations

Outcomes of Patients Undergoing the Kawashima Procedure at an Early Age: A Single Center Experience

Brian P. Bateson, Matthew Files, Lyubomyr BohutaMedical College of Georgia and Children’s Hospital of Georgia. University of Washington and Seattle Children’s Hospital.United States World Journal of Pediatric and Congenital Heart SurgeryWorld J Pediatr Congenit Heart Surg 2024; DOI: 10.1177/21501351241261361 AbstractBackground: Previous reports have demonstrated the safety and efficacy of performing early Kawashima procedure (KP). Despite this, more […]

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Congenital Lung Malformations: A Pictorial Review of Imaging Findings and a Practical Guide for Diagnosis

Giovanna Cancemi, Giulio Distefano, Gioele Vitaliti, Dario Milazzo, Giuseppe Terzo, Giuseppe Belfiore, Vincenzo Di Benedetto, Maria Grazia Scuderi, Maria Coronella, Andrea Giovanni Musumeci, Daniele Grippaldi, Letizia Antonella Mauro, Pietro Valerio Foti, Antonio Basile, Stefano PalmucciAzienda Sanitaria Provinciale di Siracusa. Azienda Sanitaria Provinciale di Ragusa and Maggiore Hospital of Modica. University Hospital Policlinico G. Rodolico-San Marco

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Early Infantile Diagnosis of Hereditary Hemorrhagic Telangiectasia Complicated by Child Abuse

Brittany Tang, Stephen Pophal, Madhusudan Ganigara, Brian Funaki, Mckenna Robinette, Veena Ramaiah, Nancy Ghanayem, Michael C. Hurley, Umesh DyamenahalliUniversity of Chicago. Indiana University.United States Journal of Pediatric Clinical PracticeJ Pediatr Clin Pract 2024; DOI: 10.1016/j.jpedcp.2024.200111 AbstractWe report a rare case of hereditary hemorrhagic telangiectasia (HHT) in a 4-month-old female infant with findings of child abuse. She

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Endothelial-to-Mesenchymal Transition in an Hereditary Hemorrhagic Telangiectasia-like Pediatric Case of Multiple Pulmonary Arteriovenous Malformations

Laura Lorente-Herraiz, Angel M. Cuesta, Lucía Recio-Poveda, Luisa M. Botella, Virginia AlbiñanaCentro de Investigaciones Biológicas Margarita Salas, CIB-CSIC. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER). Universidad Complutense de Madrid. Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC).Spain International Journal of Molecular SciencesInt J Mol Sci 2024; 25: DOI: 10.3390/ijms25116163 AbstractPulmonary arteriovenous

Endothelial-to-Mesenchymal Transition in an Hereditary Hemorrhagic Telangiectasia-like Pediatric Case of Multiple Pulmonary Arteriovenous Malformations Read More »

Objective Quantification of Bilateral Bubble Contrast Echocardiography Correlates with Systemic Oxygenation in Patients with Single Ventricle Circulation

Ashley Phimister, Chana Bushee, Monica Merbach, Sai Alekha Challa, Amy Y. Pan, Andrew D. SpearmanMedical College of Wisconsin and Children’s Wisconsin.United States Journal of Cardiovascular Development and DiseaseJ Cardiovasc Dev Dis 2024; 11: DOI: 10.3390/jcdd11030084 AbstractBubble contrast echocardiography is commonly used to diagnose pulmonary arteriovenous malformations (PAVMs) in single ventricle congenital heart disease (CHD), yet previous

Objective Quantification of Bilateral Bubble Contrast Echocardiography Correlates with Systemic Oxygenation in Patients with Single Ventricle Circulation Read More »

Phenotypic characterisation of SMAD4 variant carriers

Claire Caillot, Jean-Christophe Saurin, Valérie Hervieu, Marie Faoucher, Julie Reversat, Evelyne Decullier, Gilles Poncet, Sabine Bailly, Sophie Giraud, Sophie Dupuis-GirodFemme-Mère-Enfants Hospital and Hospices Civils de Lyon. Hôpital E. Herriot. Université Claude Bernard Lyon 1. France Journal of Medical GeneticsJ Med Genet 2024; DOI: 10.1136/jmg-2023-109632 AbstractBackground: Both hereditary haemorrhagic telangiectasia (HHT) and juvenile polyposis syndrome (JPS) are known

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Angiographic tool to detect pulmonary arteriovenous malformations in single ventricle physiology

Stephen B. Spurgin, Yousef M. Arar, Thomas M. Zellers, Jijia Wang, Nicolas L. Madsen, Surendranath R. Veeram Reddy, Ondine Cleaver, Abhay A. DivekarUniversity of Texas Southwestern Medical Center and Children’s Medical Center.United States Cardiology in the YoungCardiol Young 2024; DOI: 10.1017/S1047951124000933 AbstractObjective: Individuals with single ventricle physiology who are palliated with superior cavopulmonary anastomosis (Glenn surgery) may

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Sudden pediatric death unveiling pulmonary arteriovenous malformations

Hadeel Abu-El-Rub, Rashed Shatnawi, Yahia I. Abu Zetun, Doaa Ghorab, Ali M. ShotarYarmouk University. Mansoura University. Jordan University of Science and Technology School of Medicine.Jordan Autopsy Case ReportsAutops Case Rep 2024; DOI: 10.4322/acr.2024.489 AbstractPulmonary arteriovenous malformations (PAVMs) are abnormal vascular connections between pulmonary arteries and veins, often associated with hereditary hemorrhagic telangiectasia (HHT). Most PAVMs are

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Massive Pulmonary Arteriovenous Malformation as a Cause of Fetal Heart Failure

Joao Oliveira Dias, Ana Catarina Lai, Orlando Rodrigues, Paula Martins, Miguel Branco, Raquel Pina, António PiresCentro Hospitalar e Universitário de Coimbra.Portugal CureusCureus 2024; 16:DOI: 10.7759/cureus.52549 AbstractPulmonary arteriovenous malformations (AVMs) are abnormal connections between the pulmonary arteries and veins that can result in rapid-onset heart failure. We present a case of a fetus with pulmonary AVMs diagnosed

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Fusion imaging for guidance of pulmonary arteriovenous malformation embolisation with minimal radiation and contrast exposure

Catalina Vargas-Acevedo, Ernesto Mejia, Jenny E. Zablah, Gareth J. MorganUniversity of Colorado and Children’s Hospital Colorado.United States Cardiology in the YoungCardiol Young 2024; DOI: 10.1017/S1047951124000349 AbstractHereditary haemorrhagic telangiectasia is an inherited disorder characterised by vascular dysplasia that leads to the development of arteriovenous malformations. Pulmonary arteriovenous malformations occur in approximately 30% of patients with haemorrhagic telangiectasia.

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