• 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

XI因子缺乏继发多次关节积血后的严重踝关节关节炎:一例报告

Severe Ankle Arthritis After Multiple Hemarthrosis Secondary to Factor XI Deficiency: A Case Report.

作者信息

Douthett Steven M, Fallat Lawrence

机构信息

Third-Year Resident, Podiatric Surgical Residency Program, Beaumont Hospital-Wayne, Wayne, MI.

Program Director, Podiatric Surgical Residency Program, Beaumont Hospital-Wayne, Wayne, MI.

出版信息

J Foot Ankle Surg. 2018 Nov-Dec;57(6):1242-1245. doi: 10.1053/j.jfas.2018.03.019. Epub 2018 Jun 8.

DOI:10.1053/j.jfas.2018.03.019
PMID:29891129
Abstract

Hemophilic arthropathy of the ankle is an extremely unique condition that affects a small subset of the population in the United States. We present the case of a 66-year-old male with factor XI deficiency, which, over years of repetitive microtrauma as a professional soccer player, led to multiple hemarthrosis and severe arthropathy of his right ankle. The patient successfully underwent total ankle replacement arthroplasty and was able to return to recreational sports and competitive road cycling.

摘要

踝关节血友病性关节病是一种极为独特的病症,在美国仅影响一小部分人群。我们报告一例66岁男性,患有因子XI缺乏症,作为一名职业足球运动员,多年来反复遭受微创伤,导致右踝关节多次出血性滑膜炎和严重关节病。该患者成功接受了全踝关节置换术,能够恢复参加休闲运动和竞技性公路自行车运动。

相似文献

1
Severe Ankle Arthritis After Multiple Hemarthrosis Secondary to Factor XI Deficiency: A Case Report.XI因子缺乏继发多次关节积血后的严重踝关节关节炎:一例报告
J Foot Ankle Surg. 2018 Nov-Dec;57(6):1242-1245. doi: 10.1053/j.jfas.2018.03.019. Epub 2018 Jun 8.
2
Hemophilic arthropathy of the temporomandibular joint: review of the literature, a case report, and discussion.颞下颌关节血友病性关节病:文献综述、病例报告及讨论
Oral Surg Oral Med Oral Pathol. 1988 Feb;65(2):145-50. doi: 10.1016/0030-4220(88)90155-7.
3
Hemarthrosis revealing congenital factor XI deficiency.关节积血揭示先天性因子XI缺乏症。
Joint Bone Spine. 2008 May;75(3):348-9. doi: 10.1016/j.jbspin.2007.06.013. Epub 2008 Feb 22.
4
Orthopaedic problems about the ankle in hemophilia.血友病患者踝关节的骨科问题。
J Foot Ankle Surg. 2012 Nov-Dec;51(6):772-6. doi: 10.1053/j.jfas.2012.06.005. Epub 2012 Jul 10.
5
Open synovectomy for the prevention of recurrent hemarthrosis of the ankle in patients with hemophilia. A report of five cases with magnetic resonance imaging documentation.开放性滑膜切除术预防血友病患者踝关节复发性关节积血。五例病例报告及磁共振成像记录
Rev Rhum Engl Ed. 1997 Mar;64(3):166-71.
6
Factor XI deficiency presenting as hemarthrosis during pregnancy.妊娠期间表现为关节积血的因子XI缺乏症。
Am J Obstet Gynecol. 1987 Jul;157(1):178-9. doi: 10.1016/s0002-9378(87)80374-5.
7
Total ankle replacement for end-stage arthropathy in patients with haemophilia.血友病患者终末期关节病的全踝关节置换术。
Haemophilia. 2008 May;14(3):658-60. doi: 10.1111/j.1365-2516.2008.01650.x. Epub 2008 Feb 1.
8
Destructive monarticular arthritis secondary to anticoagulant therapy.抗凝治疗继发的破坏性单关节关节炎。
Clin Orthop Relat Res. 1987 Oct(223):247-51.
9
[Hemophiliac arthropathy of the elbow with bilateral luxation of the head of the radius. Hemophiliac arthropathy of the knee at the stage of arthrosis].
Rev Chir Oncol Radiol O R L Oftalmol Stomatol Chir. 1989 Jul-Aug;38(4):299-304.
10
Total Ankle Replacement in Hemophilia.全踝关节置换术在血友病中的应用。
Cardiovasc Hematol Disord Drug Targets. 2020;20(2):88-92. doi: 10.2174/1871529X19666191210110626.

引用本文的文献

1
A Case Report on an Extremely Rare Disease: Factor XI Deficiency.
Cureus. 2020 Oct 1;12(10):e10746. doi: 10.7759/cureus.10746.
2
A case of arthroscopic ankle arthrodesis for hemophilic arthropathy of the bilateral ankles.一例双侧踝关节血友病性关节病的关节镜下踝关节融合术病例。
Int J Surg Case Rep. 2020;74:251-256. doi: 10.1016/j.ijscr.2020.08.024. Epub 2020 Aug 29.
3
Hemophilia C: A Case Report With Updates on Diagnosis and Management of a Rare Bleeding Disorder.血友病C:一例罕见出血性疾病诊断与治疗进展的病例报告
J Hematol. 2019 Sep;8(3):144-147. doi: 10.14740/jh522. Epub 2019 Sep 30.