- VernacularTitle:妊娠38週で急性 A 型大動脈解離を発症した Marfan 症候群の1例
- Author:
Hideaki YAMABI
1
;
Akitoshi INUI
1
;
Takahiro MATSUOKA
1
;
Kousuke SIGEMATSU
2
;
Kazuhito IMANAKA
1
Author Information
- Keywords: Marfan syndrome; acute aortic dissection; Stanford type A; AAE; pregnancy
- From:Japanese Journal of Cardiovascular Surgery 2019;48(6):425-427
- CountryJapan
- Language:Japanese
- Abstract: A 34-year-old female with a gestational age of 38 weeks developed acute type A aortic dissection. Appearance of this patient was typical for Marfan's syndrome, and echocardiography revealed annulo-aortic ectasia with mild aortic regurgitation, but pericardial effusion was absent. As her hemodynamic condition was stable, an emergency Caesarean section was carried out first. After careful observation in the ICU for half a day, she successfully underwent aortic valve reimplantation and replacement of the ascending aorta under deep hypothermic circulatory arrest. Intraoperative heparin use minimally impacted uterine bleeding. Both the mother and the neonate were discharged home 16 days later. We believe a two-stage strategy should be adopted whenever possible.