“…In rare cases, MAPCAs may present with no evidence of congenital heart disease, especially in preterm neonates; they are usually small and rarely symptomatic and often regress on their own [2] . Symptomatic isolated MAPCAs have been described as having features of left-to-right shunt and present as recurrent respiratory tract infections, pulmonary hypertension, congestive cardiac failure, bronchopulmonary dysplasia, or hemoptysis [3] , [4] , [5] , [6] , [7] . Very few isolated MAPCAs have been recorded in full-term babies, and even fewer have been reported to need intervention [8] .…”