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Atresia of the common pulmonary vein

Youcef Sadou, Matteo Ciuffreda, Giancarlo CrupiOspedali Riuniti di Bergamo.Italy Cardiology in the YoungCardiol Young 2006; 16: 398-400DOI: 10.1017/S1047951106000199 AbstractA newborn girl with atresia of the common pulmonary vein, presented immediately after birth with severe cyanosis and acidosis. The diagnosis of totally obstructed total pulmonary venous return was made by cross-sectional echocardiography. Subsequent cardiac catheterization failed to […]

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Common pulmonary vein atresia: a diagnostic and therapeutic challenge

Carlos Mas, Andrew Cochrane, Samuel Menahem, Brodie KnightRoyal Children’s Hospital. Women’s and Children’s Hospital.Australia Pediatric CardiologyPediatr Cardiol 2000; 21: 490-492DOI: 10.1007/s002460010119 AbstractFollowing Doppler echocardiographic evaluation, a 16 hour-old infant underwent successful surgical repair of common pulmonary vein atresia. Investigations for prolonged postoperative ventilatory assistance, including cardiac catheterization and computerized tomography, led to a clinical diagnosis of

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Atresia of the common pulmonary vein. Case report and differential diagnosis

Myron A. Levine, James H. Moller, Kurt Amplatz, Jesse E. EdwardsUniversity of Minnesota and Charles T. Miller Hospital.United States American Journal of RoentgenologyAm J Roentgenol 1967; 100: 322-327DOI: 10.2214/ajr.100.2.322 AbstractAbstract Not Available CategoryClass II. Pulmonary Hypertension Associated with Pulmonary Vein StenosisSymptoms and Findings Associated with Pulmonary Vascular DiseaseDiagnostic Testing for Pulmonary Vascular Disease. Invasive TestingPulmonary Vascular

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Common pulmonary vein atresia

Marion K. Ledbetter, David H. Wells, Dean M. ConnorsSt. Marys Hospital Medical Center and University of WisconsinUnited States American Heart JournalAm Heart J 1978; 96: 580-586DOI: 10.1016/0002-8703(78)90193-x AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionSymptoms and Findings Associated with Pulmonary Vascular DiseaseDiagnostic Testing for Pulmonary Vascular Disease. Invasive TestingPulmonary Vascular Pathology

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Congenital Pulmonary Lymphangiectasia Masked by Postoperative Pulmonary Venous Obstruction in an Infant with Total Anomalous Pulmonary Venous Connection

Yoshiko Nawata, Daisuke Toyomura, Seigo Okada, Yasuo Suzuki, Narumi Honda-Nakada, Yuji Ohnishi, Yuichiro Sugitani, Naoki Kawaguchi, Rui Tokitaka-Okada, Naoki Masaki, Eiji Ikeda, Shunji HasegawaYamaguchi University Graduate School of Medicine. Fukuoka Children’s Hospital. Tohoku University Graduate School of Medicine.Japan International Journal of CardiologyInt J Cardiol 2024; 65: 363-366DOI: 10.1536/ihj.23-232 AbstractCongenital pulmonary lymphangiectasia (CPL) is associated with fetal

Congenital Pulmonary Lymphangiectasia Masked by Postoperative Pulmonary Venous Obstruction in an Infant with Total Anomalous Pulmonary Venous Connection Read More »

Exercise-induced Pulmonary Hypertension in Long-term Survivors of Congenital Diaphragmatic Hernia

Paul J. Critser, Terry L. Buchmiller, Kimberlee Gauvreau, Jill M. Zalieckas, Catherine A. Sheils, Gary A. Visner, Keri M. Shafer, Ming Hui Chen, Mary P. MullenBoston Children’s Hospital and Harvard Medical School. United States Journal of PediatricsJ Pediatr 2024;DOI: 10.1016/j.jpeds.2024.114034 AbstractObjective: To determine the prevalence of exercise-induced pulmonary hypertension (PH) among long-survivors of congenital diaphragmatic hernia (CDH)

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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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ABCA3 mutation-induced congenital pulmonary surfactant deficiency: A case report

Chunxia Lei, Chunhui Wan, Caixia LiuWuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College and Huazhong University of Science and Technology. Taihe Hospital and Hubei University of Medicine.China MedicineMedicine 2024; 103: DOI: 10.1097/MD.0000000000037622 AbstractIntroduction: Congenital surfactant deficiency, often caused by mutations in genes involved in surfactant biosynthesis such as ABCA3, presents a significant challenge

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Whole-Exome Sequencing Identifies DYNC2H1 Mutations as a Cause of Jeune Asphyxiating Thoracic Dystrophy Without Extra-Skeletal Organ Involvement

Ali Alsuheel Asseri, Ahmad A. Alzoani, Mohammed Almahdi, Hussein Almahdi, Nouf Almushayt, Noha Saad Alyazidi, Basmah Mohammed Al MufarrihKing Khalid University. Abha Maternity and Children Hospital and Ministry of Health. Saudi Arabia International Medical Case Reports JournalInt Med Case Rep J 2024; 17: 209-214DOI: 10.2147/IMCRJ.S447466 AbstractJeune syndrome, or asphyxiating thoracic dystrophy (JATD), is a rare autosomal

Whole-Exome Sequencing Identifies DYNC2H1 Mutations as a Cause of Jeune Asphyxiating Thoracic Dystrophy Without Extra-Skeletal Organ Involvement Read More »

Pleural Effusion and Chylothorax in Congenital Diaphragmatic Hernia-Risk Factors, Management and Outcome

Yannick Schreiner, Sidre Sahin, Christiane Otto, Meike Weis, Svetlana Hetjens, Kathrin Zahn, Michael Boettcher, Alba Perez Ortiz, Neysan RafatUniversity Children’s Hospital Mannheim, University Medical Centre Manheim and University of Heidelberg. Adolescent and Women’s Medicine, Olgahospital.Germany Journal of Clinical MedicineJ Clin Med 2024; 13:DOI: 10.3390/jcm13061764 AbstractBackground: Pleural effusion and chylothorax are common complications in the treatment of congenital

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