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http://dx.doi.org/10.1161/CIRCULATIONAHA.115.020819 | DOI Listing |
World J Pediatr Congenit Heart Surg
November 2021
Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
The association of total anomalous pulmonary venous connection (TAPVC) with aortopulmonary window (APW) is extremely rare. The coexistence of these two anomalies will have implications on clinical presentation, diagnosis, and pathophysiology. The lungs are exposed to pulmonary venous hypertension due to obstructed TAPVC as well as pulmonary arterial hypertension due to unrestrictive APW.
View Article and Find Full Text PDFWorld J Pediatr Congenit Heart Surg
January 2020
Athens Heart Surgery Institute, Iaso Children's Hospital, Athens, Greece.
Aortopulmonary window (APW) is an abnormal congenital connection between the main pulmonary artery (MPA) and the ascending aorta, with intact aortic and pulmonary valves, leading to heart failure or, if not repaired early, to pulmonary vascular obstructive disease. We report the rare case of an asymptomatic adult with an unrestrictive APW, whose pulmonary arterial hypertension was remarkably still reversible, permitting successful repair.
View Article and Find Full Text PDFCardiol Young
February 2018
1Department of Congenital Heart Disease, Royal Brompton Hospital,London,United Kingdom.
Persistence of the embryonic "fifth aortic arch" in postnatal life is a rare, enigmatic - and at times controversial - condition, with variable anatomical forms and physiological consequences. First described in humans over 40 years ago by Van Praagh, the condition was labelled the "great pretender" by Gerlis 25 years later, because of its apparent propensity to mimic anatomically similar structures. Despite many subsequent case reports citing the condition, the true developmental origin of these structures remains unresolved, and has been the subject of debate among embryologists for more than a century.
View Article and Find Full Text PDFCirculation
October 2016
From Cardiovascular Surgery (P.O.M.), Pulmonary Hypertension Program (P.O.M., M.B.), and Unit of Pediatric Cardiology (M.B.), Children's University Hospital Geneva, Geneva, Switzerland.
Circulation
October 2016
From Department of Cardiology, Chiba Children's Hospital, Chiba, Japan (T.M.); Department of Cardiology, Saiseikai Kumamoto Hospital, Kumamoto, Japan (Y.H.); and Department of Cardiology, St. Luke's International Hospital, Tokyo, Japan (K.N.).
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