Left bronchial compression and pulmonary hypertension related to anomalous right pulmonary artery

2016 ◽  
Vol 26 (5) ◽  
pp. 999-1001
Author(s):  
Jennifer A. Su ◽  
Andrew L. Cheng ◽  
Jacqueline R. Szmuszkovicz

AbstractAnomalous origin of a pulmonary artery from the ascending aorta is a congenital defect that can be complicated by pulmonary arterial hypertension, typically due to vascular disease if the anomaly is left uncorrected past 6 months of age. We describe a unique case of severe pulmonary arterial hypertension with this defect in a 1-month-old infant unexpectedly caused instead by bronchial compression from her dilated left pulmonary artery.

2019 ◽  
Vol 29 (06) ◽  
pp. 835-836 ◽  
Author(s):  
Efrén Martínez-Quintana ◽  
Jose M. Medina-Gil ◽  
Jorge Marrero-Brito

AbstractAneurysms of the pulmonary arteries and trunk are rare entities. The Waterston shunt is a palliative procedure for children with cyanotic CHD due to obstruction of the pulmonary outflow. Described complications are distortion of the pulmonary artery and pulmonary arterial hypertension. We report a patient with a giant right pulmonary artery aneurysm in relation to a Waterston shunt.


Sign in / Sign up

Export Citation Format

Share Document