Successful, Concurrent Cesarean Section and Type A Aortic Dissection Repair in a Patient With Marfan Syndrome and Sickle Cell Trait.

IF 0.6 Q4 SURGERY
Case Reports in Surgery Pub Date : 2026-06-18 eCollection Date: 2026-01-01 DOI:10.1155/cris/6391145
Emily C Scheffel, Lauryn A Ridley, Gabriel A Ramos, Jack Guiry, Beatriz Da Cruz Alves, Adanna C Akujuo
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引用次数: 0

Abstract

We present a 23-year-old at 35 weeks' gestation with Marfan syndrome (MFS) and sickle cell trait (SCT) with acute Type A aortic dissection (TAAD) requiring concurrent cesarean delivery and aortic repair. Delivery, hemi-arch aortic replacement, and coronary reconstruction were successfully performed. Despite intraoperative complexity and postoperative complications, the patient was managed with fewer ischemic complications compared to previous cases of coincident SCT and aortic repair. This case demonstrates critical principles for managing cardiothoracic emergencies in pregnancy with high-risk conditions. It emphasizes multidisciplinary care and cardiopulmonary bypass (CPB) techniques for optimization of SCT and maternal-fetal outcomes in aortopathies.

马凡氏综合征和镰状细胞特征患者成功的同时剖宫产和A型主动脉夹层修复
我们报告了一位23岁,妊娠35周的马凡氏综合征(MFS)和镰状细胞特征(SCT)合并急性a型主动脉夹层(TAAD),需要同时剖宫产和主动脉修复术。分娩、半弓主动脉置换术和冠状动脉重建均成功。尽管术中并发症和术后并发症,与之前同时进行SCT和主动脉修复的病例相比,患者的缺血性并发症较少。本病例展示了处理高危妊娠期心胸急症的关键原则。它强调多学科护理和体外循环(CPB)技术优化SCT和母胎结局主动脉病变。
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60
审稿时长
13 weeks
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