• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

颅内动脉瘤和疑似深静脉血栓形成中髂静脉发育不全所揭示的纤维肌发育不良的放射学见解。

Radiological insights into fibromuscular dysplasia unveiled by intracranial aneurysms and iliac vein hypoplasia in suspected DVT.

作者信息

Ibenyahia Abderrahmane, Elkaddouri Oumaima, Salek Mounir, Boustani Salma, Bigi Soufiane, Adnor Said, Bouissar Wassila, Wakrim Soukaina

机构信息

Radiology Department, University Hospital Center of Souss Massa, Faculty of Medicine and Pharmacy, Ibn Zohr Agadir University, Agadir, Morocco.

Department of Internal Medicine, Faculty of Medicine and Pharmacy of Agadir, University Ibn Zohr, Agadir, Morocco.

出版信息

Radiol Case Rep. 2024 Dec 31;20(3):1631-1636. doi: 10.1016/j.radcr.2024.12.025. eCollection 2025 Mar.

DOI:10.1016/j.radcr.2024.12.025
PMID:39845280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11750457/
Abstract

Fibromuscular Dysplasia (FMD) is a nonatherosclerotic, noninflammatory vascular disorder predominantly affecting women aged 18 to 65 years. This case report highlights a 74-year-old female diagnosed with FMD incidentally during evaluation for deep vein thrombosis (DVT). Imaging revealed significant vascular anomalies, including a giant intracranial carotid aneurysm and a hypoplastic iliac vein with extensive collateral formation. Early detection and tailored management are crucial to prevent complications such as arterial dissections, aneurysms, and stroke. The patient showed favorable evolution without anticoagulation therapy, and interventional embolization was planned to mitigate rupture risks. Differential diagnosis includes atherosclerotic aneurysms, Ehlers-Danlos syndrome, Marfan syndrome, neurofibromatosis type 1, and polyarteritis nodosa, which must be distinguished through comprehensive imaging and clinical evaluation. The prognosis of FMD varies widely and depends on the extent and location of arterial involvement. This case underscores the importance of advanced imaging in accurately diagnosing and guiding long-term follow-up for FMD management.

摘要

纤维肌发育不良(FMD)是一种非动脉粥样硬化、非炎症性血管疾病,主要影响18至65岁的女性。本病例报告重点介绍了一名74岁女性,她在接受深静脉血栓形成(DVT)评估时偶然被诊断为FMD。影像学检查显示有明显的血管异常,包括巨大的颅内颈动脉瘤和发育不全的髂静脉并伴有广泛的侧支形成。早期检测和针对性治疗对于预防动脉夹层、动脉瘤和中风等并发症至关重要。该患者在未接受抗凝治疗的情况下病情进展良好,并计划进行介入栓塞以降低破裂风险。鉴别诊断包括动脉粥样硬化性动脉瘤、埃勒斯-当洛综合征、马方综合征、1型神经纤维瘤病和结节性多动脉炎,必须通过全面的影像学和临床评估加以区分。FMD的预后差异很大,取决于动脉受累的程度和部位。本病例强调了先进影像学在准确诊断和指导FMD管理的长期随访中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/f748c096de99/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/becd38ff4197/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/22b6cb63014c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/61e7445b811b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/e7d1ecbc362d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/f568508be442/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/51d8fd097209/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/46529dc1c993/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/f748c096de99/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/becd38ff4197/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/22b6cb63014c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/61e7445b811b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/e7d1ecbc362d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/f568508be442/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/51d8fd097209/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/46529dc1c993/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5cc/11750457/f748c096de99/gr8.jpg

相似文献

1
Radiological insights into fibromuscular dysplasia unveiled by intracranial aneurysms and iliac vein hypoplasia in suspected DVT.颅内动脉瘤和疑似深静脉血栓形成中髂静脉发育不全所揭示的纤维肌发育不良的放射学见解。
Radiol Case Rep. 2024 Dec 31;20(3):1631-1636. doi: 10.1016/j.radcr.2024.12.025. eCollection 2025 Mar.
2
A Retrospective Cohort Study of Cerebrovascular Fibromuscular Dysplasia.一项关于脑血管纤维肌性发育异常的回顾性队列研究。
Ann Vasc Surg. 2023 May;92:104-110. doi: 10.1016/j.avsg.2022.12.092. Epub 2023 Jan 13.
3
Prevalence of Intracranial Aneurysm in Women With Fibromuscular Dysplasia: A Report From the US Registry for Fibromuscular Dysplasia.纤维肌发育不良女性颅内动脉瘤的患病率:来自美国纤维肌发育不良登记处的报告。
JAMA Neurol. 2017 Sep 1;74(9):1081-1087. doi: 10.1001/jamaneurol.2017.1333.
4
Fibromuscular dysplasia.纤维肌性发育异常
Orphanet J Rare Dis. 2007 Jun 7;2:28. doi: 10.1186/1750-1172-2-28.
5
Fibromuscular dysplasia of cervicocephalic arteries: Prevalence of multisite involvement and prognosis.颈脑动脉纤维肌发育不良:多部位受累的患病率及预后
Rev Neurol (Paris). 2015 Sep;171(8-9):616-23. doi: 10.1016/j.neurol.2015.02.011. Epub 2015 Apr 7.
6
Histopathologic features of intracranial vascular involvement in fibromuscular dysplasia, ehlers-danlos type IV, and neurofibromatosis I.纤维肌性发育异常、IV型埃勒斯-当洛综合征及I型神经纤维瘤病中颅内血管受累的组织病理学特征
J Neuropathol Exp Neurol. 2014 Oct;73(10):916-32. doi: 10.1097/NEN.0000000000000113.
7
Fibromuscular dysplasia - results of a multicentre study in Flanders.纤维肌性发育异常——弗拉芒地区一项多中心研究的结果
Vasa. 2017 May;46(3):211-218. doi: 10.1024/0301-1526/a000613. Epub 2017 Feb 3.
8
Bilateral common iliac artery aneurysms secondary to fibromuscular dysplasia accompanied with a coronary aneurysm. A case report.
J Cardiovasc Surg (Torino). 1995 Dec;36(6):587-90.
9
Fibromuscular dysplasia: its various phenotypes in everyday practice in 2021.纤维肌性发育不良:2021 年日常实践中的各种表型。
Kardiol Pol. 2021;79(7-8):733-744. doi: 10.33963/KP.a2021.0040. Epub 2021 Jun 24.
10
High flow bypass for right giant cavernous internal carotid artery aneurysm with fibromuscular dysplasia of cervical internal carotid artery: microsurgical 2-D video.用于治疗伴有颈内动脉纤维肌发育异常的右侧巨大海绵窦段颈内动脉瘤的高流量搭桥术:显微外科二维视频
Surg Neurol Int. 2020 Jul 4;11:177. doi: 10.25259/SNI_141_2020. eCollection 2020.

本文引用的文献

1
Congenital absence of the left external iliac vein with anomalous venous connection in a pediatric patient.一名儿科患者出现左髂外静脉先天性缺如并伴有异常静脉连接。
J Vasc Surg Cases Innov Tech. 2023 Feb 20;9(2):101134. doi: 10.1016/j.jvscit.2023.101134. eCollection 2023 Jun.
2
Prevalence and manifestations of diagnosed fibromuscular dysplasia by sex and race: Analysis of >4500 FMD cases in the United States.按性别和种族划分的纤维肌发育不良的诊断患病率和表现:美国超过 4500 例 FMD 病例分析。
Heart Lung. 2021 Jan-Feb;50(1):168-173. doi: 10.1016/j.hrtlng.2020.09.022. Epub 2020 Oct 15.
3
Epidemiology of fibromuscular dysplasia: A review of the literature.
纤维肌性发育异常的流行病学:文献综述
Vasc Med. 2016 Aug;21(4):376-81. doi: 10.1177/1358863X16637913. Epub 2016 Apr 11.
4
Fibromuscular dysplasia of arteries of the head and neck: imaging findings.头颈部动脉纤维肌发育不良:影像学表现
AJR Am J Roentgenol. 1994 May;162(5):1205-9. doi: 10.2214/ajr.162.5.8166011.