Pulmonary artery agenesis refers to a rare congenital absence of pulmonary artery due to a malformation in the sixth aortic arch. It can occur bilaterally, with both left and right pulmonary arteries being absent, or unilaterally, the absence of either left or right pulmonary artery (UAPA). About 67% of UAPA occurs isolated in the right lung.[1] The absence of pulmonary artery can be an isolated disorder, or accompanied by other related lesions,[2] most commonly Tetralogy of Fallot.[3]
Back in 1868, Fraentzel was the first to report isolated unilateral absence of pulmonary artery (IUAPA) in literature.[4][5] Subsequently, literature has documented a total of 420 cases.[6] The estimated prevalence of IUAPA is 1 in 200,000 adults.[2] No sex preference is observed.[6] Patients with severe complications are usually diagnosed early in age while adult patients are mainly asymptomatic. The overall mortality rate reaches 7%.[7]
Individuals may exhibit a variety of symptoms, or they may not exhibit any symptoms at all. Recurrent lung infections and exercise intolerance are some of the most common symptoms.[8] Serious complications include hemoptysis and pulmonary hypertension. These non-specific symptoms make UAPA challenging to diagnose.[9] Multiple medical imaging techniques are often employed in combination in order to obtain a comprehensive diagnosis.[8]