Literature DB >> 10097476

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

T Ueda1, H Shimizu, R Aeba, H Shin, T Katogi, R Yozu, S Kawada.   

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.

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Year:  1999        PMID: 10097476     DOI: 10.1007/bf03217945

Source DB:  PubMed          Journal:  Jpn J Thorac Cardiovasc Surg        ISSN: 1344-4964


  15 in total

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  6 in total

Review 1.  Aortic dissection in osteogenesis imperfecta: case report and review of the literature.

Authors:  Michael F McNeeley; Brian N Dontchos; Michael A Laflamme; Michal Hubka; Claudia T Sadro
Journal:  Emerg Radiol       Date:  2012-04-20

2.  Clinical outcomes of aortic repair in young adult patients with ACTA2 mutations.

Authors:  Yoshimasa Seike; Kenji Minatoya; Hiroaki Sasaki; Hiroshi Tanaka; Tatsuya Itonaga; Yosuke Inoue; Hiroko Morisaki; Takayuki Morisaki; Hatsue Ishibashi-Ueda; Junjiro Kobayashi
Journal:  Gen Thorac Cardiovasc Surg       Date:  2017-08-14

3.  Surgical treatment for cardiovascular lesions of patients with Marfan syndrome.

Authors:  Fumio Yamazaki; Mitsuomi Shimamoto; Shoji Fujita; Masanao Nakai; Tomoya Kono; Akihiro Aoyama; Fengshi Chen; Tomohiro Nakata
Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2002-09

4.  Genetic variants in Chinese patients with sporadic Stanford type A aortic dissection.

Authors:  Zhao-Ran Chen; Ming-Hui Bao; Xing-Yu Wang; Yan-Min Yang; Bi Huang; Zhong-Li Han; Jun Cai; Xiao-Han Fan
Journal:  J Thorac Dis       Date:  2021-07       Impact factor: 2.895

5.  Ruptured isolated external iliac artery true aneurysm associated with cystic medial necrosis: report of a case.

Authors:  Takayoshi Kato; Hisato Takagi; Norikazu Kawai; Yasutomo Sekido; Takuya Umemoto
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6.  Extended total arch replacement for type B aortic dissection with ascending aneurysm following healed aortic dissection.

Authors:  Yoshie Ochiai; Kazuhiro Kurisu; Takashi Kajiwara; Hiroshi Kumeda; Ryuji Tominaga
Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2004-02
  6 in total

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