Thoracic endovascular aortic repair using a Najuta thoracic fenestrated stent graft for type B aortic dissection with an aberrant right subclavian artery

Q4 Medicine
Journal of Cardiology Cases Pub Date : 2026-03-01 Epub Date: 2026-01-20 DOI:10.1016/j.jccase.2026.01.002
Tatsuya Ozaki MD , Taro Nakazato MD, PhD , Yosuke Hata MD , Katsukiyo Kitabayashi MD, PhD
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Abstract

An aberrant right subclavian artery (ARSA) is a rare vascular malformation, and the surgical treatment of aortic diseases in patients with ARSA often necessitates the use of specialized techniques depending on the location of its orifice. Herein, we report a case of chronic Stanford type B aortic dissection (TBAD) with ARSA and false lumen perfusion of the abdominal branches; entry tear closure was achieved through thoracic endovascular aortic repair (TEVAR) using a fenestrated stent graft while preserving false lumen perfusion. The patient was a 48-year-old man with a 3-year history of acute TBAD with ARSA. Outpatient computed tomography revealed dissecting aortic aneurysm enlargement (>5 mm) over 6 months. As the celiac and superior mesenteric arteries were supplied by the false lumen and only small re-entry tears were identified in the bilateral external iliac arteries, the risk of intestinal ischemia due to stent-graft closure of the entry tear was recognized. To preserve false lumen perfusion, a new re-entry tear was created using a guidewire and percutaneous transluminal angioplasty balloon catheter under intravascular ultrasound guidance, followed by debranching TEVAR with a Najuta thoracic fenestrated stent graft (Kawasumi Laboratories, Inc., Tokyo, Japan). The patient had an uneventful postoperative course and was discharged on postoperative day 10.

Learning objective

Entry tear closure with thoracic endovascular aortic repair for type B aortic dissection with an aberrant right subclavian artery often requires complex cervical debranching; however, the use of a Najuta thoracic fenestrated stent graft may simplify the surgical procedure. If the abdominal branches are perfused by the false lumen and the re-entry tear is small, the creation of a new re-entry tear using a guidewire and percutaneous transluminal angioplasty balloon catheter under intravascular ultrasound guidance is a practical approach for preserving false lumen blood flow.
右锁骨下动脉异常的B型主动脉夹层胸椎开窗支架的血管内修复。
异常右锁骨下动脉(ARSA)是一种罕见的血管畸形,ARSA患者的主动脉疾病的手术治疗通常需要根据其开口的位置使用专门的技术。在此,我们报告一例慢性Stanford B型主动脉夹层(TBAD)合并ARSA和腹支假腔灌注;在保留假腔灌注的同时,通过胸椎血管内主动脉修复术(TEVAR)实现入口撕裂闭合。患者为48岁男性,有3年急性TBAD伴ARSA病史。门诊计算机断层扫描显示夹层主动脉瘤增大(bbb50 mm)超过6 个月。由于乳糜和肠系膜上动脉由假腔供应,双侧髂外动脉仅发现小的再入性撕裂,因此认识到支架关闭进入性撕裂导致肠道缺血的风险。为了保持假腔灌注,在血管内超声引导下,使用导丝和经皮腔内血管成形术球囊导管形成新的再入撕裂,然后使用Najuta胸椎开窗支架(Kawasumi Laboratories, Inc., Tokyo, Japan)去分支TEVAR。患者术后顺利,于术后第10天出院。学习目的:胸腔血管内主动脉修补术治疗B型主动脉夹层伴右侧锁骨下动脉异常,通常需要复杂的颈椎去分支;然而,使用Najuta胸椎开窗支架可以简化手术过程。如果腹部分支被假腔灌注,再入撕裂很小,在血管内超声引导下使用导丝和经皮腔内血管成形术球囊导管制造新的再入撕裂是一种保留假腔血流的实用方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Cardiology Cases
Journal of Cardiology Cases Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
177
审稿时长
59 days
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