Endovascular repair of infrarenal aortic aneurysm and severe stenosis in Type V Takayasu arteritis: a rare case report and clinical insights.

Much Muzakky Misbachul Firdaus, Zakiyyatul Aflakha, Yusuf Aji Samudera Nurrobi, Johannes Nugroho Eko Putranto
{"title":"Endovascular repair of infrarenal aortic aneurysm and severe stenosis in Type V Takayasu arteritis: a rare case report and clinical insights.","authors":"Much Muzakky Misbachul Firdaus, Zakiyyatul Aflakha, Yusuf Aji Samudera Nurrobi, Johannes Nugroho Eko Putranto","doi":"10.1186/s43044-025-00702-7","DOIUrl":null,"url":null,"abstract":"<p><p>BACKGROUND: Takayasu arteritis (TA) is a rare, chronic vasculitis affecting the aorta and its major branches, leading to stenosis, aneurysm, and ischemic complications. It primarily affects young adults and may progress to critical ischemia, necessitating revascularization strategies. Endovascular aneurysm repair (EVAR) is increasingly recognized as an effective, minimally invasive intervention for managing TA-associated complications. CASE DESCRIPTION: A 28-year-old male presented with a three-month history of progressive bilateral lower limb discomfort and tingling exacerbated by activity, intermittent abdominal cramps, and fatigue. Physical examination revealed a significant blood pressure discrepancy between the upper limbs (right: 193/66 mmHg, left: 100/71 mmHg), reduced lower limb pressures (right ankle: 66/41 mmHg, left ankle: 72/42 mmHg), pulse deficits, and diminished ankle-brachial indices (right: 0.34; left: 0.37). Transthoracic echocardiography (TTE) demonstrated all-chamber dilatation, reduced systolic function (EF: 38%), severe mitral regurgitation, moderate aortic regurgitation, and a large right atrial thrombus (3.0 × 1.9 cm). Computed tomography angiography (CTA) revealed critical mid-aortic stenosis (6.9 × 11.9 mm), a post-stenotic saccular aneurysm (20.6 × 22.4 mm), and severe narrowing of the left subclavian and axillary arteries. The patient underwent endovascular aneurysm repair (EVAR), with a thoracic stent graft (24 × 80 mm) successfully deployed. Six months post-procedure, the patient experienced complete resolution of symptoms, with improved ABI values (right: 0.94; left: 0.73) and significant regression of the aneurysm (13.1 × 13.1 mm). CONCLUSION: EVAR may represent a feasible option for carefully selected TA patients with focal lesions and high surgical risk, although open repair remains necessary for more complex disease. Lifelong surveillance and further research are essential to optimize management strategies in this rare condition. </p>","PeriodicalId":74993,"journal":{"name":"The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology","volume":"77 1","pages":"108"},"PeriodicalIF":0.0000,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12675888/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s43044-025-00702-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND: Takayasu arteritis (TA) is a rare, chronic vasculitis affecting the aorta and its major branches, leading to stenosis, aneurysm, and ischemic complications. It primarily affects young adults and may progress to critical ischemia, necessitating revascularization strategies. Endovascular aneurysm repair (EVAR) is increasingly recognized as an effective, minimally invasive intervention for managing TA-associated complications. CASE DESCRIPTION: A 28-year-old male presented with a three-month history of progressive bilateral lower limb discomfort and tingling exacerbated by activity, intermittent abdominal cramps, and fatigue. Physical examination revealed a significant blood pressure discrepancy between the upper limbs (right: 193/66 mmHg, left: 100/71 mmHg), reduced lower limb pressures (right ankle: 66/41 mmHg, left ankle: 72/42 mmHg), pulse deficits, and diminished ankle-brachial indices (right: 0.34; left: 0.37). Transthoracic echocardiography (TTE) demonstrated all-chamber dilatation, reduced systolic function (EF: 38%), severe mitral regurgitation, moderate aortic regurgitation, and a large right atrial thrombus (3.0 × 1.9 cm). Computed tomography angiography (CTA) revealed critical mid-aortic stenosis (6.9 × 11.9 mm), a post-stenotic saccular aneurysm (20.6 × 22.4 mm), and severe narrowing of the left subclavian and axillary arteries. The patient underwent endovascular aneurysm repair (EVAR), with a thoracic stent graft (24 × 80 mm) successfully deployed. Six months post-procedure, the patient experienced complete resolution of symptoms, with improved ABI values (right: 0.94; left: 0.73) and significant regression of the aneurysm (13.1 × 13.1 mm). CONCLUSION: EVAR may represent a feasible option for carefully selected TA patients with focal lesions and high surgical risk, although open repair remains necessary for more complex disease. Lifelong surveillance and further research are essential to optimize management strategies in this rare condition.

Abstract Image

Abstract Image

Abstract Image

V型高须动脉炎肾下动脉瘤及严重狭窄的血管内修复:罕见病例报告及临床见解。
背景:高松动脉炎(Takayasu arteritis, TA)是一种罕见的影响主动脉及其主要分支的慢性血管炎,可导致狭窄、动脉瘤和缺血性并发症。它主要影响年轻人,并可能发展为严重缺血,需要血运重建策略。血管内动脉瘤修复(EVAR)越来越被认为是一种有效的、微创的治疗ta相关并发症的干预手段。病例描述:一名28岁男性患者,三个月的进行性双侧下肢不适和刺痛病史,活动、间歇性腹部痉挛和疲劳加剧。体格检查显示上肢血压差异明显(右:193/66 mmHg,左:100/71 mmHg),下肢血压降低(右脚踝:66/41 mmHg,左脚踝:72/42 mmHg),脉搏不足,踝关节-肱指数降低(右:0.34,左:0.37)。经胸超声心动图(TTE)显示全室扩张,收缩功能降低(EF: 38%),严重二尖瓣反流,中度主动脉反流,大右心房血栓(3.0 × 1.9 cm)。ct血管造影(CTA)显示主动脉中部严重狭窄(6.9 × 11.9 mm),狭窄后囊状动脉瘤(20.6 × 22.4 mm),左侧锁骨下动脉和腋窝动脉严重狭窄。患者接受了血管内动脉瘤修复术(EVAR),成功放置了一个24 × 80 mm的胸腔支架。术后6个月,患者症状完全缓解,ABI值改善(右:0.94,左:0.73),动脉瘤明显缩小(13.1 × 13.1 mm)。结论:对于有局灶性病变和手术风险高的精心挑选的TA患者,EVAR可能是一种可行的选择,尽管对于更复杂的疾病,开放修复仍然是必要的。终身监测和进一步研究对于优化这种罕见疾病的管理策略至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书