Japanese Journal of Vascular Surgery
Online ISSN : 1881-767X
Print ISSN : 0918-6778
Case Reports
A Case of Four-channel Aortic Dissection
Shogo Oyama Shingo OhuchiIwao OnoYukinobu Ito
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JOURNAL OPEN ACCESS

2017 Volume 26 Issue 1 Pages 41-44

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Abstract

Four-channel aortic dissection is rare. We reported our experience that we had performed an operation for four-channel aortic dissection because the aortic dissection had gotten worse from a three-channel aortic dissection and its diameter had extended. Our case was a 44-year-old woman with Marfan syndrome. She undewent a Bentall procedure and total arch replacement for Stanford A aortic dissection in 2008. Her postoperative course was uneventful. So, we requested observation of her condition to a local doctor. She underwent a CT in 2014. We found her descending aortic dissection changed to a three-channel aortic dissection. Next year, she was taken to another hospital via ambulance for sudden back pain. Then, her descending aorta’s diameter extended and her three-channel aortic dissection changed four-channel aortic dissection. A week later, her descending aortic diameter extended further. So she was transferred to our hospital. We performed a thoracoabdominal aortic replacement. Her postoperative course was uneventful, and she was discharged without incident. Four-aortic dissection is high risk of rupture, so we think such cases need surgical treatment as soon as possible.

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https://creativecommons.org/licenses/by-nc-sa/4.0/deed.ja
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