Pulmonary Vascular Pathology

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 »

Common pulmonary vein atresia. Premortem diagnosis in two infants

Richard E. Hawker, John M. Celermajer, Don C. Gengos, Timothy B. Cartmill, J. Denby BowdlerRoyal Alexandra Hospital for Children.Australia CirculationCirculation 1972; 46: 368-374DOI: 10.1161/01.cir.46.2.368 Abstract (Summary)Two cases of common pulmonary vein atresia (CPVA) are presented. In one, the diagnosis was suspected on clinical grounds, and in both it was confirmed by cardiac catheterization and angiocardiography. Surgical

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Common pulmonary vein atresia without anomalous pulmonary venous connection

Charles T. DeLise, Bernard Schneider, Marie S. BlackmanUpstate Medical Center, Syracuse.United States Pediatric RadiologyPediatr Radiol 1979; 8: 195-197DOI: 10.1007/BF00973835 AbstractCommon pulmonary vein atresia without pulmonary venous connection is a rare form of congenital heart disease. No communication exists between the confluence of the pulmonary veins and the heart or a major systemic vessel. A case diagnosed

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Incidence of alveolar capillary dysplasia with misalignment of pulmonary veins in infants with unexplained severe pulmonary hypertension: The roles of clinical, pathological, and genetic testing

Tetsuo Onda, Takuma Akimoto, Itaru Hayasaka, Masahiko Ikeda, Yuta Furuse, Akiko Ando, Yuichi Nakamura, Ryota Honjo, Atsushi Manabe, Itsuko Furuta, Kazutoshi ChoHokkaido University Hospital. Japan Early Human DevelopmentEarly Hum Dev 2021; 155:DOI: 10.1016/j.earlhumdev.2021.105323 AbstractBackground: Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a rare and fatal disorder that occurs in the developing fetal lungs; at

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Atresia of the common pulmonary vein

Jaya R. Deshpande, Suman G. KinareSeth G.S. Medical College.India International Journal of CardiologyInt J Cardiol 1991; 30: 221-226DOI: 10.1016/0167-5273(91)90099-b AbstractIn our study of 1326 autopsied cases of congenital heart disease, we have encountered 3 cases of atresia of the common pulmonary vein. This is a rare condition of which, to the best part of our knowledge,

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Atresia of the common pulmonary vein–a rare congenital anomaly

Pradeep Vaideeswar, Milind S. Tullu, Pragati A. Sathe, Ruchi NanavatiSeth G.S. Medical College and KEM Hospital.India Congenital Heart DiseaseCongenit Heart Dis 2008; 3: 431-434DOI: 10.1111/j.1747-0803.2008.00225.x AbstractObjectives: Early atresia of the common pulmonary vein (ACPV) leads to total anomalous pulmonary venous drainage, while late atresia or incomplete absorption leads to common pulmonary vein atresia and cor triatriatum sinister

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Pulmonary vasculature development in congenital diaphragmatic hernia: a novel automated quantitative imaging analysis

Emrah Aydin, Furkan Durmus, Nilhan Torlak, Marc Oria, Nilgün Güler Bayazit, Esin Öztürk Isik, Birol Aslanyürek, Jose L. PeiroCincinnati Children’s Hospital Medical Center and University of Cincinnati College of Medicine. Boğaziçi University. Yildiz Technical University.United States and Turkey Pediatric Surgery InternationalPediatr Surg Int 2024; 40:DOI: 10.1007/s00383-024-05643-x AbstractPurpose: Impaired fetal lung vasculature determines the degree of pulmonary hypertension

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Twins with alveolar capillary dysplasia with misalignment of pulmonary veins: Strategies for diagnosis and management

Sinead Brady, Usha Krishnan, Anjali Saqi, Diana VargasNew York Presbyterian-Morgan Stanley Children’s Hospital and Columbia University Irving Medical Center.United States Journal of Neonatal-Perinatal MedicineJ Neonatal Perinatal Med 2024; 17: 147-152DOI: 10.3233/NPM-230085 AbstractWe present a case of dichorionic-diamniotic twin females who developed hypoxemic respiratory failure. They were ultimately diagnosed by lung biopsy with alveolar capillary dysplasia with

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c-Myc Drives inflammation of the maternal-fetal interface, and neonatal lung remodeling induced by intra-amniotic inflammation

April W. Tan, Xiaoying Tong, Silvia Alvarez-Cubela, Pingping Chen, Aline Guimarães Santana, Alejo A. Morales, Runxia Tian, Rae Infante, Vanessa Nunes de Paiva, Shathiyah Kulandavelu, Merline Benny, Juan Dominguez-Bendala, Shu Wu, Karen C. Young, Claudia O. Rodrigues, Augusto F. SchmidtUniversity of Miami Miller School of Medicine and Holtz Children’s Hospital. Florida Atlantic University Charles E.

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Increased Elastase and Matrix Metalloproteinase Levels in the Pulmonary Arteries of Infants With Congenital Diaphragmatic Hernia

Jui-Hsia Hung, Stéphanie Langlois, Meagen Weibe, Benjamin Wild, Jessica Barré-Dunn, Kyle N. CowanUniversity of Ottawa and Children’s Hospital of Eastern Ontario. Canada Journal of Pediatric SurgeryJ Pediatr Surg 2024;DOI: 10.1016/j.jpedsurg.2024.01.028 AbstractBackground: Pulmonary vascular disease (PVD) complicated with pulmonary hypertension (PH) is a leading cause of mortality in congenital diaphragmatic hernia (CDH). Unfortunately, CDH patients are often resistant

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