Friso M. Rijnberg, Hans C. van Assen, Joe F. Juffermans, Lucia J. M. Kroft, Pieter J. van den Boogaard, Patrick J. H. de Koning, Mark G. Hazekamp, Séline F. S. van der Woude, Evangeline G. Warmerdam, Tim Leiner, Heynric B. Grotenhuis, Jelle J. Goeman, Hildo J. Lamb, Arno A. W. Roest, Jos J. M. WestenbergLeiden […]
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
Isolated agenesis of the right pulmonary veins with pulmonary sequestration Read More »
Mirjana Miksić, Faris Mujezinović, Maruša Selič Serdinšek, Miha Weiss, Sergej PrijićUniversity Medical Centre. University of Belgrade.Slovenia and Serbia American Journal of Case ReportsAm J Case Rep 2020; 21:DOI: 10.12659/AJCR.923162 AbstractBackground: Scimitar syndrome (SCS) is a rare congenital cardiopulmonary malformation, characterized by anomalous pulmonary venous drainage from the right lung associated with aortopulmonary collateral arteries and pulmonary
A Scimitar Syndrome Variant Associated with Critical Aortic Coarctation in a Newborn Read More »
Siavosh Khonsari, Peter W. Saunders, Martin H. Lees, Albert StarrOregon Health Sciences University.United States Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 1982; 83: 443-448DOI: https://doi.org/10.1016/S0022-5223(19)37282-4 AbstractCommon pulmonary vein atresia is a rare congenital anomaly; all four pulmonary veins drain into a common dilated chamber with no direct connections to the heart or systemic
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
Common pulmonary vein atresia. Premortem diagnosis in two infants Read More »
O. Dominguez Garcia, M. A. Granados Ruiz, M. D. Sanchez Redondo, M. Lázaro Salvador, R. Juarez TosinaHospital Virgen de la Salud.Spain Pediatric CardiologyPediatr Cardiol 2009; 30: 989-991DOI: 10.1007/s00246-008-9320-2 AbstractA newborn female experienced severe respiratory distress immediately after delivery. She presented with intense cyanosis, refractory hypoxemia, and acidosis. The deterioration was rapidly progressive, leading to the child’s
A difficult emergency surgical diagnosis: atresia of the common pulmonary vein Read More »
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
Common pulmonary vein atresia without anomalous pulmonary venous connection Read More »
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
Yuki Nakamura, Kagami Miyaji, Yurie Miyata, Atsushi KitagawaKitasato University Hospital.Japan Annals of Thoracic SurgeryAnnThorac Surg 2016; 101: 2382-2384DOI: 10.1016/j.athoracsur.2015.08.085 AbstractWe describe an unusual case of a newborn with a rare variant of atresia of the common pulmonary vein that was mistaken for total anomalous pulmonary venous connection, cardiac type. The survival of patients with atresia of
An Extremely Rare Variant of Pulmonary Venous Atresia Read More »
T. Suzuki, M. Sato, T. Murai, T. FukudaTokyo Metropolitan Children’s Hospital.Japan Pediatric CardiologyPediatr Cardiol 2001; 22: 255-257DOI: 10.1007/s002460010217 AbstractA 7-hour-old boy underwent an emergency operation with an anticipated diagnosis of total anomalous pulmonary venous connection. The precise diagnosis of common pulmonary vein atresia (CPVA) was made during the operation. A side-to-side anastomosis between the common pulmonary
Successful surgical repair of common pulmonary vein atresia in a newborn Read More »
