Systemic to Pulmonary Arterial Collaterals or Connections Associated with Pulmonary Vascular Disease

A translational framework for patient-specific modeling of pulmonary vein stenosis

Manish Bansal, Jeffrey S. Heinle, Athar M. Qureshi, Ravi K. BirlaTexas Children’s Hospital Heart Center and Baylor College of Medicine. United States Journal of Thoracic and Cardiovascular Surgery OpenJTCVS Open 2026; DOI: 10.1016/j.xjon.2026.101858 AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionReview Articles Concerning Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular […]

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Multimodal imaging of infantile scimitar syndrome with Eisenmenger physiology: A case report of complex intracardiac and extracardiac shunts

Berihu Gebre, Yirgalem Gereziher, Catherine Alcober, Gladys Baltazar, Viachaslau MarkauNauru Medical Center. Mekelle University.Republic of Nauru and Ethiopia Radiology Case ReportsRadiol Case Rep 2026; 21: 4642-4650DOI: 10.1016/j.radcr.2026.06.141 AbstractScimitar syndrome is a rare congenital vascular malformation in which the right pulmonary veins drain abnormally into the inferior vena cava, right atrium, or portal vein instead of the

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Expanding the phenotypic and genotypic spectrum of KCNT1-related epilepsies

Mathilde Gras, Gaelle Quentin-Romand, Nicole Chemaly, Giulia Barcia, KCNT1 consortium and Rima NabboutNecker Enfants Malades Hospital and Université Paris Cité. France Brain CommunicationsBrain Commun 2026; 8: DOI: 10.1093/braincomms/fcag256 AbstractThe KCNT1 gene encodes for a sodium-activated potassium channel involved in neuronal excitability. Since its initial description in 2012 in patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS)

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Anomalous origin of the right pulmonary artery from the ascending aorta: a case report and review of the literature

Alwaleed Al-Dairy, Ali Deeb, Zakaria Aldammad, Ahmad Al-BitarDamascus University. Syrian Arab Republic (Syria) International Journal of Surgery Case ReportsInt J Surg Case Rep 2026; 138: 2278-2282DOI: 10.1097/RC9.0000000000000526 AbstractIntroduction: Anomalous aortic origin of a pulmonary artery (AORPA), or hemitruncus arteriosus, is a rare congenital anomaly in which one pulmonary artery arises directly from the ascending aorta. Without timely

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Major Aortopulmonary Collateral Artery as a Rare Cause of Heart Failure in a Neonate with Transposition of the Great Arteries: An Unexpected Turn in an Otherwise Routine Case

Vojislav Parezanovic, Dusan Andric, Vladimir Chadikovski, Vedran Stojanovikj, Jordanka Madzoska, Vesna Trpkovska, Igor StefanovicUniversity Children’s Hospital and University of Belgrade. Acibadem Sistina Hospital.Serbia Journal of Cardiovascular Development and DiseaseJ Cardiovasc Dev Dis 2026; 13: DOI: 10.3390/jcdd13050210 AbstractThe association of a major aortopulmonary collateral artery (MAPCA) with simple transposition of the great arteries (TGA) is uncommon. Such

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Two Uncomplicated Vaginal Deliveries in a Woman With Scimitar Syndrome: A Case Report

Motoki Tanabe, Toshiyuki Itai, Chika Akamatsu, Shinya Kondo, Rie Nakashima, Shun Kawai, Yuichi Imai, Etsuko MiyagYokohama City University School of Medicine. Japan CureusCureus 2026; 18: DOI: 10.7759/cureus.104674 AbstractScimitar syndrome is a rare, complex congenital cardiopulmonary venous anomaly characterized by anomalous drainage of the right pulmonary vein into the inferior vena cava, hypoplasia of the right lung,

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Transcatheter closure of anomalous systemic arterial supply to the left lung from the left subclavian artery: Diagnostic and procedural challenges

Anil Kumar Singhi, Manojit Lodha, Santunu De, Arpita Choraria, Sandip Sardar, Ejaz Ahmed Bari, Debadri ChakrabartiManipal Hospital EM Bypass. Vivekananda Institute of Medical Sciences. India Journal of Cardiology CasesJ Cardiol Cases 2025 Aug 5; 32: 207-210DOI: 10.1016/j.jccase.2025.07.007 AbstractA 26-year-old woman with chronic effort intolerance and a continuous murmur underwent evaluation for suspected congenital heart disease. While

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Congenital descending aorta to pulmonary vein fistula: an unusual cause of left ventricular dilation in a 21-year-old female

Xiang Pan, Chan Yu, Zhouhui Chen, Bowen ZhaoSir Run Run Shaw Hospital and Zhejiang University College of Medicine.China Journal of Cardiothoracic SurgeryJ Cardiothorac Surg 2025; 20: DOI: 10.1186/s13019-025-03691-5 AbstractBackground: Congenital descending aorta to pulmonary vein fistula (cDAPVF) is a rare congenital vascular malformation diagnosed in infancy and childhood. Adult cDAPVF is often asymptomatic and usually detected incidentally

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Protective Effects of Bronchopulmonary Sequestration (BPS) on the Prognosis of Neonates with Congenital Diaphragmatic Hernia (CDH)

Sujin Gang, Yong Jae Kwon, Hyunhee Kwon, Suhyun Ha, Jueun Park, Byong Sop Lee, Euiseok Jung, Jiyoon Jeong, Soo Hyun Kim, Jung-Man NamgoongAsan Medical Center Children’s Hospital, Asan Medical Center and Jeonbuk National University Hospital. University of Ulsan College of Medicine. Gangneung Asan Hospital.Republic of Korea BioMedical Central PediatricsBMC Prediatr 2025; 25: DOI: 10.1186/s12887-025-05755-w AbstractBackground: Congenital diaphragmatic

Protective Effects of Bronchopulmonary Sequestration (BPS) on the Prognosis of Neonates with Congenital Diaphragmatic Hernia (CDH) Read More »

Unilateral Pulmonary Vein Atresia in a Child

Jia-Bei Liu, Peng LiuFirst Affiliated Hospital of Hunan Normal University and Hunan Provincial People’s Hospital.China Pediatric PulmonologyPediatr Pulmonol 2025; 60:DOI: 10.1002/ppul.27378 AbstractWe describe a case of unilateral pulmonary vein atresia in a child who presented with a recurrent cough. Pulmonary artery CT angiography confirmed the diagnosis. In addition, we found anomalous blood-supplying arteries from the abdominal

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