Complicated type B aortic dissection in a pregnant woman with Marfan syndrome

被引：0

作者：

Zagzoog, Mohammad M. ^{[1
,2
]}

Crawford, Sean A. ^{[3
]}

Davaine, Jean-Michel ^{[1
,2
]}

机构：

[1] Sorbonne Univ, Pitie Salpetriere Univ Hosp, Fac Med, Dept Vasc & Endovasc Surg, Paris, France

[2] Sorbonne Univ, Fac Med, Paris, France

[3] Univ Hlth Network, Toronto Gen Hosp, Peter Munk Cardiac Ctr, Toronto, ON, Canada

来源：

JOURNAL OF VASCULAR SURGERY CASES INNOVATIONS AND TECHNIQUES | 2024年 / 10卷 / 05期

关键词：

Aortic dissection; Retrograde type A aortic dissection; Pregnancy; Marfan syndrome; Thoracic endovascular aortic repair; MORTALITY; GROWTH; REPAIR; WOMEN;

D O I：

10.1016/j.jvscit.2024.101561

中图分类号：

R61 [外科手术学];

学科分类号：

摘要：

Marfan syndrome is a rare inherited connective tissue disorder that can result in significant fi cant morbidity and mortality. We report a case of a 29-year-old pregnant woman presenting with an acute type B aortic dissection. Owing to cardiopulmonary decompensation and intestinal malperfusion, she underwent an emergency cesarean section followed by left subclavian to carotid transposition and thoracic endovascular aortic repair that was complicated by a retrograde type A aortic dissection and was managed surgically. Molecular testing confirmed fi rmed the diagnosis of Marfan syndrome. This case highlights that multidisciplinary and hybrid management of challenging cases of acute aortic syndromes can result in a favorable outcome. (J Vasc Surg Cases Innov Tech 2024;10:101561.)

引用

页数：3

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