Skip to main content
Log in

Prognosis of Marfan and non-Marfan patients with cystic medial necrosis of the aorta

  • Original Article
  • Published:
The Japanese Journal of Thoracic and Cardiovascular Surgery Aims and scope Submit manuscript

Abstract

The characteristics and prognosis of patients with cystic medial necrosis of the aorta were reviewed. Subjects were 46 patients who underwent aortic and/or aortic valve surgery between August 1965 and October 1994. All had histologically documented cystic medial necrosis including 22 Marfan patients. The patients with Marfan syndrome were substantially younger (median age, 32 vs 50 years; p<0.05), and experienced annulo-aortic ectasia more frequently (81%(17/22) vs 46%(11/24); p<0.05 than those without the syndrome. Sixty-eight percent (15/22) of the Marfan patients and 63% (15/24) of the non-Marfan patients experienced complications with aortic dissection, although not to a significant degree. The hospital mortality rate was 14% (3/22) in the Marfan group and 21% (5/24) in the non-Marfan group, which was also not significant. Of the 38 survivors, developments in the health of 37 were completely followed-up until October 1997. The cardiovascular event-free rate for Marfan patients at 10 years (28%) was lower than that for non-Marfan patients (68%, p=0.057), whereas the actuarial survival rates at 10 years were nearly equal (72% for the Marfan patients and 74% for the non-Marfan patients). Reoperation was the first cardiovascular event in 77% (10/13) of the Marfan patients and in 14% (1/7) of the non-Marfan patients (p<0.05). Cardiovascular event was the main cause of late death both for Marfan patients (80%; 4/5) and for non-Marfan patients (86%; 6/7). In conclusion, independent of the presence of Marfan syndrome, careful follow-up is necessary for patients with cystic medial necrosis of the aorta to eliminate serious late complications.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Shumacker HB. Cystic medial necrosis. J Cardiovasc Surg 1978; 19: 639–45.

    Google Scholar 

  2. Erdheim J. Medionecrosis aortae idiopathica cystica. Virchows Arch [A] 1929; 270: 187–229.

    Google Scholar 

  3. Ellis PR, Cooley DA, DeBakey ME. Clinical considerations and surgical treatment of annulo-aortic ectasia. J Thorac Cardiovasc Surg 1961; 42: 363–70.

    PubMed  CAS  Google Scholar 

  4. Savunen T, Aho HJ. Annulo-aortic ectasia. Light and microscopic changes in aortic media. Virchows Arch [A] 1985; 407: 279–88.

    Article  CAS  Google Scholar 

  5. Roberts WC, Honig HS. The spectrum of cardiovascular disease in the Marfan syndrome. A clinicomorphologic study of 18 necropsy patients and comparison to 151 previously reported necropsy patients. Am Heart J 1992, 104; 115–35

    Article  Google Scholar 

  6. Beighton P, de Paepe A, Danks D, Finidori G. International nosology of heritable disorders of connective tissue, Berlin, 1986. Am J Med Genet 1988; 29: 581–94.

    Article  PubMed  CAS  Google Scholar 

  7. Savunen T. Cardiovascular abnormalities in the relatives of patients operated upon for annulo-aortic ectasia: a clinical and echocardiographic study of 40 families. Eur J Cardio-thorac Surg 1987; 1: 3–10

    Article  CAS  Google Scholar 

  8. Murdoch JL, Walker BA, Halpern BL, Kuzuma JW, McKusick VA. Life expectancy and causes of death in the Marfan syndrome. N Engl J Med 1972; 286: 804–8.

    Article  PubMed  CAS  Google Scholar 

  9. Marsalese DL, Moodie DS, Lytle BW, Cosgrove DM, Ratliff NB, Goormastic M, Kovacs A. Cystic medial necrosis of the aorta in patients without Marfan’s syndrome: surgical outcome and long-term follow-up. J Am Coll Cardiol 1990; 16: 68–73.

    Article  PubMed  CAS  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  11. Svensson LG, 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-I–42.

    Google Scholar 

  12. Gott VL, Pyeritz RE, Cameron DE, Greene PS, McKusick VA. Composite graft repair of Marfan aneurysm of the ascending aorta: results in 100 patients. Ann Thorac Surg 1991; 52: 38–45.

    Article  PubMed  CAS  Google Scholar 

  13. Pyeritz RE. Predictors of dissection of the ascending aorta in Marfan syndrome. Circulation 1991; 84: II-351.

    Google Scholar 

  14. El Habbal MH. Cardiovascular manifestations of Marfan’s syndrome in the young. Am Heart J 1992 123: 752–7

    Article  PubMed  Google Scholar 

  15. Gott VL, Cameron DE, Reitz BA, Pyeritz RE. Current diagnosis and prescription for the Marfan syndrome: aortic root and valve replacement. J Card Surg 1994; 9(Suppl): 177–81

    Article  PubMed  CAS  Google Scholar 

  16. Trotter SE, Olsen EGJ. Marfan’s disease and Erdheim’s cyctic medionecrosis. A study of their pathology. Eur Heart J 1991; 12: 83–7.

    PubMed  CAS  Google Scholar 

  17. Bentall HH, DeBono A. A technique for complete replacement of the ascending aorta. Thorax 1968; 23: 338–9.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ueda, T., Shimizu, H., Aeba, R. et al. Prognosis of Marfan and non-Marfan patients with cystic medial necrosis of the aorta. Jpn J Thorac Caridovasc Surg 47, 73–78 (1999). https://doi.org/10.1007/BF03217945

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03217945

Index words

Navigation