Page 4 - Virtual Vascular Vol 6
P. 4

Coarctation of Aorta






                                                                                                                            A young man with history of aortic
                                                                                                                            coarctation and spinal scoliosis presented

                                                                                                                            with cold lower extremities. Coarctation is
                                                                                                                            a congenital condition whereby the aorta

                                                                                                                            is narrow, usually in the area where the
                                                                                                                            ductus arteriosus inserts.










                                                                                                                            At the age of 7, this patient had a bypass
                                                                                                                            from the ascending to the descending
                                                                                                                            thoracic aorta as a procedure to treat his

                                                                                                                            hypoplastic arch. The CT scan performed
                                                                                                                            after 20 years showed that the bypass
                                                                                                                            graft is patent.


















                                                                                                                                                            Coarctation.mp4







            About 60-80% of adult Marfan Syndrome patients eventually de-
            velop an aortic root aneurysm.  This is a serious condition and the

            patient is at risk of Type A Aortic dissection, rupture, aortic valve

            incompetence, heart failure and myocardial infarction.  This patient
            has a huge root aneurysm and should be electively repaired by as-

            cending and valve replacement.  The AAA can be treated at a sec-

            ond stage with open aneurysm repair.





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