Literature DB >> 9271733

Bentall operation for a child with Marfan syndrome: a case report.

M Miura1, Y Shimazaki, T Watanabe, Y Iijima, S Kuraoka, K Inui, T Oshikirl, T Uchida, M Nakasato.   

Abstract

Children with Marfan syndrome rarely undergo surgery for annuloaortic ectasia and aortic regurgitation in the first decade. A 7-year-old girl presented with congestive heart failure due to severe aortic regurgitation associated with annuloaortic ectasia (6 cm). She also had funnel chest. She underwent a Bentall operation and sternal turn-over with a satisfactory result. Since the aortic valve cusps had rolled edges, the aortic valve was not spared. Histology of the aortic valve cusps showed myxoid degeneration and fragmentation of elastic fibers.

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Year:  1997        PMID: 9271733     DOI: 10.1111/j.1540-8191.1997.tb00106.x

Source DB:  PubMed          Journal:  J Card Surg        ISSN: 0886-0440            Impact factor:   1.620


  1 in total

1.  Mitral valve replacement and subsequent composite graft replacement of the aortic root for infantile Marfan syndrome.

Authors:  Y Kamikubo; T Murashita; K Yasuda; J Matano; K Sakai
Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2000-06
  1 in total

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