Interact CardioVasc Thorac Surg 2007;6:256. doi:10.1510/icvts.2006.149187A © 2007 European Association of Cardio-Thoracic Surgery
Case report - Vascular thoracic |
ICVTS on-line discussion A Women with Marfan syndrome
Mohamed Fahmy Ibrahim and
Amal A. Refaut
PSHC, King Fahd Medical City, Riyadh, Saudi Arabia
Recurrent type B intramural hematoma progressed into type A acute aortic dissection in a young otherwise healthy woman: are there unknown background factors?
eComment: Concerning the case report described by Baek et al. [1], we recently encountered a multiparous woman with Marfan syndrome in her 8th week of gestation who presented with acute type A aortic dissection. After reviewing the literature, it seems that pregnancy is a risk factor for the development of aortic dissection in this subset of patients. My question is about the history of pregnancy in Baek's patient. I also agree with the author's comment in the discussion that the frozen elephant technique would have been a perfect option for this patient. Another option would be to tackle the ascending aorta surgically, as done by Baek et al., and then as a hybrid technique to deploy a percutaneous stent graft for the distal intimal disruption.
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Reference
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- Baek WK, Yoon YH, Kim JT, Kim KH. Recurrent type B intramural hematoma progressed into type A acute aortic dissection in a young otherwise healthy woman: are there unknown background factors? Interact CardioVasc Thorac Surg 2007; 6:255256.[Abstract/Free Full Text]
Related Article
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Recurrent type B intramural hematoma progressed into type A acute aortic dissection in a young otherwise healthy woman: are there unknown background factors?
- Wan Ki Baek, Yong Han Yoon, Joung Taek Kim, and Kwang Ho Kim
Interactive CardioVascular and Thoracic Surgery 2007 6: 255-256.
[Abstract]
[Full Text]
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