“…1,2 Congenital atresia of the LMCA is a very rare disease, and only a small number of reports have been published. 3 In the present case, the absence of aortitis, Kawasaki disease history, calcium deposits, arteriosclerosis, and of continuity between the LMCA and the proximal tip of the LAD suggested a congenital phenotype. Furthermore, on CTA the LAD was occluded, with no evidence of ostial stamp of the LAD distal tip, and the proximal tip of the LAD seemed to approach the main pulmonary artery while leaving a trabecular trace.…”