A Case of Neonatal Marfan Syndrome Requiring Double Atrioventricular Valve Replacement due to Rapid Exacerbation of the Repaired Valves

  • Ogata Yuki
    Cardiovascular Surgery, Kagoshima City Hospital
  • Shigehisa Yoshiya
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Yamashita Yushi
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Matsuba Tomoyuki
    Cardiovascular Surgery, Kagoshima City Hospital
  • Toyokawa Kenji
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Kanda Hideaki
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Kawaida Keisuke
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Kuramoto Shinya
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Soga Yoshiharu
    Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
  • Imoto Yutaka
    Cardiovascular Surgery, Fujimoto General Hospital

Bibliographic Information

Other Title
  • 両房室弁形成後の逆流急性増悪のために2弁置換を行った新生児Marfan症候群の1例

Search this article

Abstract

<p>Neonatal Marfan syndrome is the most severe form of Marfan syndrome usually showing critical cardio-respiratory symptoms from the neonatal period or early infancy. We report a boy with this syndrome who presented with heart failure at 3 months of age and was referred to our department at 6 months old after intense medical treatment. He had enophthalmos, funnel chest, arachnodactyly, and Steinberg's thumb sign, but had no family history of Marfan syndrome or other cardiac diseases. Left ventricular dilatation, severe mitral regurgitation and moderate tricuspid regurgitation were noted on echocardiography. Mitral valvuloplasty and tricuspid annuloplasty were performed, and the regurgitation improved to trivial and mild level, respectively. However, rapid exacerbation of mitral regurgitation occurred, and the patient fell into circulatory collapse which needed circulatory support with extracorporeal membrane oxygenator (ECMO) on 18th postoperative day. In the emergency operation, the previous surgical procedures on the mitral valve were intact and we thought that rapid progression of the mitral annular dilatation and valve expansion to be the cause of exacerbation. Mitral valve replacement (Regent® 21 mm aortic) was performed, and the cardiac function improved, but ECMO was still needed because of the depressed respiratory function. Furthermore, tricuspid regurgitation due to annular dilatation and valve expansion was aggravated rapidly which needed tricuspid valve replacement (ATS® 20 mm mitral) 9 days after the mitral valve replacement. ECMO was ceased on the 37th day and the patient was extubated on 71st day. He was discharged from the hospital 5 months after the first operation. One year has passed after discharge, and he is doing well with anticoagulation. In the treatment of neonatal Marfan syndrome, surgical procedure for valve repair is still controversial and it should be remembered that rapid exacerbation of the atrioventricular valve can occur even after satisfactory valve repair and there should be no hesitation regarding surgical intervention when needed.</p>

Journal

References(8)*help

See more

Details 詳細情報について

Report a problem

Back to top