Absence of the pulmonary artery

A rare vascular anomaly characterized by congenital absence of the right or left pulmonary artery, usually ending within 2 cm of its expected origin from the pulmonary trunk. Patients often also have other cardiovascular abnormalities and respective symptoms and are then typically diagnosed in infancy or childhood, while isolated cases generally present with a mild clinical course and may go undiagnosed until adulthood. Presenting clinical features in isolated cases include hemoptysis, exertional dyspnea, and recurrent respiratory infections. The condition is typically accompanied by marked changes of lung tissue and may, if unrecognized, result in massive hemoptysis and pulmonary hypertension.

Also known as: UAPA, agenesis of pulmonary artery, aplasia of pulmonary artery, pulmonary artery absent, pulmonary artery agenesis, unilateral pulmonary artery absence, unilateral pulmonary artery agenesis, congenital absence of pulmonary artery

2 clinical trials for this condition and its sub-types, 1 tagged with Absence of the pulmonary artery itself.