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A surgical case of acute three-channeled aortic dissection in Marfan syndrome

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Abstract

We surgically treated a 35-year-old male with acute 3- channeled aortic dissection in Marfan syndrome. He had acute type A aortic dissection, and underwent Bentall’s type operation, simultaneous graft replacement of the ascending aorta and total aortic arch. Pain recurred 5 years and 9 months after the first operation. CT scan showed two adjacent false lumens in the descending aorta. The morphology of the first and second dissections was Stanford type A+B. The second dissection was acute. In the second false lumen, a re-entry formation was observed in the abdominal aorta. Because severe pain was persistent, we immediately replaced the descending aorta using a femoro-femoral partial cardiopulmonary bypass. The patient was doing well and was discharged. When pain recurs in a Marfan patient with an aortic dissection, a 3-channeled aortic dissection should be suspected, and we recommend emergency surgery.

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References

  1. McReynolds RA, Shin MS, Sims RD. Three-channeled aortic dissection. Am J Roentgenol 1978; 130: 549–52.

    CAS  Google Scholar 

  2. Svensson JG, Crawford ES, Coselli JS, Safi HJ, Hess KR. Impact of cardiovascular operation on survival in the Marfan patient. Circulation 1989; 80 (Suppl I): I–233-42.

    Google Scholar 

  3. Jovanovic R, Kanjuh V, Papo I, Pecija B, Latkovic Z, Kanjuh S. Marfan syndrome with aortic dissection and triple-barrel aorta. Am J Cardiovasc Pathol 1992; 4: 19–24.

    PubMed  CAS  Google Scholar 

  4. Daily PO, Trueblood HW, Stinson EB, Wuerflein RD, Shumway NE. Management of acute aortic dissections. Ann Thorac Surg 1970; 10: 237–47.

    Article  PubMed  CAS  Google Scholar 

  5. DeBakey ME, Henly WS, Cooley DA, Morris GC, Crawford ES, Beall AC. Surgical management of dissecting aneurysms of the aorta. J Thorac Cardiovasc Surg 1965; 49: 130–49.

    PubMed  CAS  Google Scholar 

  6. Larson EW, Edwards WD. Risk factors for aortic dissection: a necropsy study of 161 cases. Am J Cardiol 1984; 53: 849–55.

    Article  PubMed  CAS  Google Scholar 

  7. Pyeritz RE, McKusick VA. The Marfan syndrome: diagnosis and management. N Engl J Med 1979; 300: 772–7.

    Article  PubMed  CAS  Google Scholar 

  8. Crawford ES. Marfan syndrome: broad spectral surgical treatment cardiovascular manifestations. Ann Surg 1983; 198: 487–505.

    Article  PubMed  CAS  Google Scholar 

  9. DeBakey ME, McCollum CH, Crawford ES, et al. Dissection and dissecting aneurysms of the aorta: twenty-year follow-up of five hundred twenty-seven patients treated surgically. Surgery 1982; 92: 1118–34.

    PubMed  CAS  Google Scholar 

  10. Crawford ES, Crawford JL, Stowe CL, Safi HJ. Total aortic replacement for chronic aortic dissection occurring in patients with and without Marfan’s syndrome. Ann Surg 1984; 199: 358–62.

    Article  PubMed  CAS  Google Scholar 

  11. Finkbohner R, Johnston D, Crawford ES, Coselli J, Milewicz DM. Marfan syndrome: long-term survival and complications after aortic aneurysm repair. Circulation 1995; 91: 728–33.

    PubMed  CAS  Google Scholar 

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Ando, M., Takamoto, S., Okita, Y. et al. A surgical case of acute three-channeled aortic dissection in Marfan syndrome. Jpn J Thorac Caridovasc Surg 46, 949–952 (1998). https://doi.org/10.1007/BF03217852

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  • DOI: https://doi.org/10.1007/BF03217852

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