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

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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Concurrent Bronchopulmonary Sequestration in Congenital Diaphragmatic Hernia: Is Frequency Increasing or Are We Better at Diagnosis?

Michelle J. Yang, Christian C. Yost, Martha Monson, Paula J. Woodward, Anne M. Kennedy, Stephen J. Fenton, Katie W. Russell, Janice L. B. Byrne, Bradley A. YoderPrimary Children’s Hospital and University of Utah School of Medicine.United States Journal of Pediatrics: Clinical PracticeJ Pediatr Clin Pract 2025; DOI: 10.1016/j.jpedcp.2025.200141 AbstractObjective: To assess the incidence and clinical outcomes of

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Esophageal varices in association with unilateral pulmonary vein atresia

J. Kevin Harrison, Steven E. Hearne, William M. Baker, Peter Van Trigt, Gil Leidig, Thomas M. Bashore, Martin P. O’LaughlinDuke University Medical Center.United States Catheterization and Cardiovascular DiagnosesCathet Cardiovasc Diagn 1996; 38: 387-392DOI: 10.1002/(SICI)1097-0304(199608)38:4<387::AID-CCD14>3.0.CO;2-C AbstractA 27-yr-old woman with recurrent episodes of hemoptysis (and hematemesis due to esophageal varices) was found to have unilateral pulmonary vein atresia.

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Cardiac phenotypic spectrum of KCNT1 mutations

Utkarsh Kohli, Chitra Ravishankar, Douglas NordliComer Children’s Hospital and Pritzker School of Medicine of the University of Chicago. he Children’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania. United States Cardiology in the YoungCardiol Young 2020; 30: 1935-1939DOI: 10.1017/S1047951120002735 AbstractWe report a 10-month-old girl with KCNT1 (c1420C > T; p. Arg474Cys,

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Isolated agenesis of the right pulmonary veins with pulmonary sequestration

Shilpa Patil, Sakshi Sachdeva, Shweta Bakhru, Bharat Dalvi, Nageswara Rao KonetiCare Hospital. Glenmark Cardiac Center. India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2019; 12: 135-137DOI: 10.4103/apc.APC_55_18 AbstractWe report two cases of agenesis of the right pulmonary veins (PVs) associated with sequestration of the right lung with systemic to pulmonary collateral. Both the children were referred for

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