3型洛伊迪茨综合征合并MYH11共突变术中主动脉夹层的外科治疗
Surgical Management of Intraoperative Aortic Dissection in Type 3 Loeys-Dietz Syndrome with MYH11 Co-Mutation.
作者信息
Yoneyama Fumiya, Kato Hideyuki, Mathis Bryan, Hiramatsu Yuji
机构信息
Department of Cardiovascular Surgery, University of Tsukuba, Tsukuba, Japan.
出版信息
Heart Surg Forum. 2021 Mar 3;24(2):E231-E232. doi: 10.1532/hsf.3533.
DOI:10.1532/hsf.3533
PMID:33798051
Abstract
A 57-year-old female with Loeys-Dietz syndrome type 3 and MYH11 gene mutation underwent unexpected intraoperative ascending aortic dissection and subsequent rapid progression of the aortic arch dissecting aneurysm. Intra-surgical contingency plans with regard to aortic dissection and aneurysm should be considered for Loeys-Dietz syndrome, especially with comorbid mutations.
摘要
一名患有3型洛伊斯-迪茨综合征和MYH11基因突变的57岁女性在术中意外发生升主动脉夹层，并随后出现主动脉弓夹层动脉瘤的快速进展。对于洛伊斯-迪茨综合征，尤其是伴有合并突变的情况，应考虑制定关于主动脉夹层和动脉瘤的术中应急计划。
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