Cystic medial necrosis of the aorta in patients without Marfan's syndrome: surgical outcome and long-term follow-up
DL Marsalese,
DS Moodie,
BW Lytle,
DM Cosgrove,
NB Ratliff,
M Goormastic,
and
A Kovacs
Department of Cardiology, Cleveland Clinic Foundation, Ohio 44195-5066.
A retrospective analysis was performed to determine the surgical outcome and long-term follow-up of patients with documented cystic medial necrosis of the aorta. Ninety-three patients were diagnosed as having cystic medial necrosis at the Cleveland Clinic between July 1963 and December 1987 (72% men aged 26 to 77 years, mean 55). Patients who met the standard diagnostic criteria for Marfan's syndrome were deliberately excluded. Sixty-eight percent of the patients had a diastolic murmur and chest roentgenogram revealed a dilated aortic arch in 58% and cardiomegaly in 63%. Cardiac catheterization in 76 patients demonstrated aortic root dilation in 78%, aortic regurgitation in 72%, aortic dissection in 32% and coronary artery disease in 32%. Ninety patients underwent surgery including composite graft repair with reimplantation of the coronary arteries in 34%. Follow-up, obtained on 90 (97%) of the 93 patients, ranged in duration from 0 to 137 months (mean 29). Thirty-four of the 90 patients died (age range 30 to 75 years, mean 60). Ninety-four percent of the known causes of death were related to the cardiovascular system; 65% were the result of aortic dissection or rupture or sudden death. Ninety-six percent of survivors were in New York Heart Association functional class I or II. Overall estimated survival at 1, 3 and 5 years was 72.2%, 63.5% and 57.4%, respectively. Actuarial survival in patients who underwent composite graft reconstruction was 84% at 5 years. The presence of a diastolic murmur at initial presentation was associated with a poor prognosis (p = 0.03).(ABSTRACT TRUNCATED AT 250 WORDS)
This article has been cited by other articles:

|
 |

|
 |
 
E. Girdauskas, M. A. Borger, M.-A. Secknus, G. Girdauskas, and T. Kuntze
Is aortopathy in bicuspid aortic valve disease a congenital defect or a result of abnormal hemodynamics? A critical reappraisal of a one-sided argument
Eur J Cardiothorac Surg,
June 1, 2011;
39(6):
809 - 814.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Matt, D. L. Huso, J. Habashi, T. Holm, J. Doyle, F. Schoenhoff, G. Liu, J. Black, J. E. Van Eyk, and H. C. Dietz
Murine model of surgically induced acute aortic dissection type A
J. Thorac. Cardiovasc. Surg.,
April 1, 2010;
139(4):
1041 - 1047.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Vahanian, B. Iung, L. Pierard, R. Dion, and J. Pepper
CHAPTER 21 Valvular Heart Disease
ESC Textbook of Cardiovascular Medicine,
January 1, 2009;
2(1):
med-9780199566990-chapter - med-9780199566990-chapter.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Girdauskas, T. Kuntze, M. A. Borger, T. Doenst, M. Mochalski, T. Walther, V. Falk, and F. W. Mohr
Long-Term Prognosis of Type A Aortic Dissection in Non-Marfan Patients With Histologic Pattern of Cystic Medial Necrosis
Ann. Thorac. Surg.,
March 1, 2008;
85(3):
972 - 977.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A.-M. Heegaard, A. Corsi, C. C. Danielsen, K. L. Nielsen, H. L. Jorgensen, M. Riminucci, M. F. Young, and P. Bianco
Biglycan Deficiency Causes Spontaneous Aortic Dissection and Rupture in Mice
Circulation,
May 29, 2007;
115(21):
2731 - 2738.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Farhat, M. Durand, L. Boussel, I. Sanchez, J. Villard, and O. Jegaden
Should a reimplantation valve sparing procedure be done systematically in type A aortic dissection?
Eur J Cardiothorac Surg,
January 1, 2007;
31(1):
36 - 41.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Caraang and A. El-Bialy
Case Report: Aortic Dissection and Cystic Medial Degeneration in a 24-Year-Old Without Marfan Syndrome
Journal of Cardiovascular Pharmacology and Therapeutics,
October 1, 2004;
9(4):
299 - 302.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Giusti, M. C. Porciani, T. Brunelli, L. Evangelisti, S. Fedi, G. F. Gensini, R. Abbate, G. Sani, M. Yacoub, and G. Pepe
Phenotypic variability of cardiovascular manifestations in Marfan Syndrome: Possible role of hyperhomocysteinemia and C677T MTHFR gene polymorphism
Eur. Heart J.,
November 2, 2003;
24(22):
2038 - 2045.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. S. Absi, T. M. Sundt III, W. S. Tung, M. Moon, J. K. Lee, R. R. Damiano Jr, and R. W. Thompson
Altered patterns of gene expression distinguishing ascending aortic aneurysms from abdominal aortic aneurysms: complementary DNA expression profiling in the molecular characterization of aortic disease
J. Thorac. Cardiovasc. Surg.,
August 1, 2003;
126(2):
344 - 357.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. G. Leyh, S. Fischer, K. Kallenbach, T. Kofidis, K. Pethig, W. Harringer, and A. Haverich
High Failure Rate After Valve-sparing Aortic Root Replacement Using the "Remodeling Technique" in Acute Type A Aortic Dissection
Circulation,
September 24, 2002;
106(12_suppl_1):
I-229 - I-233.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Iung, C. Gohlke-Barwolf, P. Tornos, C. Tribouilloy, R. Hall, E. Butchart, and A. Vahanian
Recommendations on the management of the asymptomatic patient with valvular heart disease
Eur. Heart J.,
August 2, 2002;
23(16):
1253 - 1266.
[PDF]
|
 |
|

|
 |

|
 |
 
R. G. Leyh, C. Schmidtke, C. Bartels, and H.-H. Sievers
Valve-sparing aortic root replacement (remodeling/reimplantation) in acute type A dissection
Ann. Thorac. Surg.,
July 1, 2000;
70(1):
21 - 24.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M Groenink, T A J Lohuis, J G P Tijssen, M S J Naeff, R C M Hennekam, E E van der Wall, and B J M Mulder
Survival and complication free survival in Marfan's syndrome: implications of current guidelines
Heart,
October 1, 1999;
82(4):
499 - 504.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. A. Ergin, D. Spielvogel, A. Apaydin, S. L. Lansman, J. N. McCullough, J. D. Galla, and R. B. Griepp
Surgical treatment of the dilated ascending aorta: when and how?
Ann. Thorac. Surg.,
June 1, 1999;
67(6):
1834 - 1839.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. A. Dodds III, C. A. Warnes, and G. K. Danielson
AORTIC VALVE REPLACEMENT AFTER REPAIR OF PULMONARY ATRESIA AND VENTRICULAR SEPTAL DEFECT OR TETRALOGY OF FALLOT
J. Thorac. Cardiovasc. Surg.,
April 1, 1997;
113(4):
736 - 741.
[Abstract]
[Full Text]
|
 |
|
|