“…From the viewpoint of reconstructive vascular surgery, such symptomatic anomalous coronary arteries branching from the pulmonary trunk/arteries have been noted (Backer et al, 1992). Concerning the anomalies of the aortic arch, right-sided aortic arches of the type-N anomaly, such as the present case, often seem to be asymptomatic (Koizumi et al, 1994), whereas type M right-sided aortas (type III-A after Stewart-Edwards) are reported to be accompanied at high frequency by various cardiac malformations, such as tetralogy of Fallot (Glew and Hartnell, 1991;Craatz et al, 2003). The right-sided type N aortas are always accompanied by a retroesophageal aortic diverticulum (Kommerell's diverticulum), which may cause dysphagia and dyspnea (Stö rk et al, 2001;Morel et al, 2002), although no clinical data was available in this case.…”