二尖瓣经导管边缘对边缘修补术作为治疗主动脉夹层动脉瘤的桥梁,用于一例马凡氏综合征患者:病例报告

Takanori Kawamoto, Tomohito Kogure, Chihiro Koyanagi, Kyomi Ashihara, Junichi Yamaguchi
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引用次数: 0

摘要

马凡氏综合征是一种遗传性疾病,表现为各种心血管疾病。本病例报告讨论了一名并发主动脉瘤破裂和急性二尖瓣反流(MR)的马凡综合征患者,并探讨了这一独特病例的治疗策略。 一名被诊断为马凡氏综合征的 57 岁男性患者出现进行性呼吸困难并伴有呼吸困难。诊断为急性心力衰竭(HF),起因于与腱索破裂相关的急性 MR。然而,对比增强 CT 显示同时存在巨大的主动脉夹层动脉瘤,这表明需要进行手术治疗。剥离性主动脉瘤的范围很大。考虑到与二尖瓣同时手术的高风险,手术采取了分阶段进行的方式。首先进行二尖瓣经导管边缘到边缘修补术(MV-TEER),以降低围手术期高频风险,然后按计划对剥离的主动脉瘤进行两阶段手术。这一策略有效地促进了在 MV-TEER 术后的慢性期对剥离的主动脉瘤进行手术干预。 一些报告显示,MV-TEER 在手术风险较高的退行性 MR 病例中效果显著,但在马凡综合征中 MV-TEER 的病例报告并不多见。近年来,也有报道称 MV-TEER 可作为心脏移植的 "桥梁疗法"。MV-TEER被认为是一种潜在的选择,可作为其他侵入性干预的桥梁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitral valve transcatheter edge-to-edge repair as a bridge to treat aortic dissecting aneurysm in a case of Marfan syndrome: A case report
Marfan syndrome is an inherited disorder that manifests with various cardiovascular conditions. This case report discusses a patient with Marfan syndrome presenting with concurrent dissecting aortic aneurysm and acute mitral valve regurgitation (MR), exploring treatment strategies for this unique case. A 57-year-old man diagnosed with Marfan syndrome presented with progressive dyspnea and awareness of orthopnea. Acute heart failure (HF) due to acute MR associated with chordae rupture was diagnosed. However, contrast-enhanced CT revealed the coexistence of a massive dissecting aortic aneurysm, indicating surgical intervention. The dissecting aortic aneurysm extended over a large area. Given the high risk of simultaneous surgery with the mitral valve, a staged approach was adopted. Mitral valve transcatheter edge-to-edge repair (MV-TEER) was performed as the initial step to reduce the perioperative HF risk, followed by a planned two-stage surgery for the dissecting aortic aneurysm. This strategy effectively facilitated surgical intervention for the dissecting aortic aneurysm in the chronic phase after MV-TEER. Several reports showed the effectiveness of MV-TEER in cases of degenerative MR where surgical operation carries a high risk, but case report of MV-TEER in Marfan syndrome is rare. In recent years, the effectiveness of MV-TEER has also been reported as a “bridge therapy” for heart transplantation. MV-TEER is considered a potential option to serve as a bridge to other invasive intervention.
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