Pulmonary artery aneurysm (PAA) is a rare anomaly with an autopsy prevalence of 1:14,000. [1][2][3] These aneurysms can arise secondary to various etiologies such as congenital heart disease (CHD), connective-tissue disorders, acquired vascular diseases (infections, vasculitis), malignancy, trauma, iatrogenic causes, or, rarely, they can be idiopathic. 2,4 Most patients remain undiagnosed due to its silent course and non-specific clinical manifestations. 1,4 However, lethal complications, including pulmonary artery (PA) dissection, rupture, massive hemoptysis, and acute coronary syndrome from vessel compression, have been reported. 5 PAAs generally occur in a younger age group than aortic aneurysms, with no gender predilection. 6