向安德烈·文森特教授(1931-2023)致敬。

IF 0.6 4区 医学 Q4 ORTHOPEDICS Acta orthopaedica Belgica Pub Date : 2024-09-01 DOI:10.52628/90.3.12751
O Cornu, T Schubert, X Libouton, K Tribak, D Putineanu, M VAN Cauter, L Kaminski, E Thienpont, P-L Docquier, X Banse, J-E Dubuc, O Barbier
{"title":"向安德烈·文森特教授(1931-2023)致敬。","authors":"O Cornu, T Schubert, X Libouton, K Tribak, D Putineanu, M VAN Cauter, L Kaminski, E Thienpont, P-L Docquier, X Banse, J-E Dubuc, O Barbier","doi":"10.52628/90.3.12751","DOIUrl":null,"url":null,"abstract":"<p><p>Alkaptonuria (AKU) is an extremely rare autosomal recessive metabolic disorder caused by deficiency of homogentisic acid oxidase and resulting in accumulation of homogentisic acid in collagenous structures. It is characterized by a triad of homogentisic aciduria, bluish-black discoloration of connective tissues (ochronosis) and arthropathy of large weight bearing joints. We report on a middle-aged female patient with bilateral severe ochronotic arthritis of both hips and shoulder joints requiring total joint replacements as staged procedures which were done without complications offering a complete pain relief and a satisfactory clinical and functional outcome. Ochronosis can cause severe arthropathy of peripheral joints. Multiple joint affection is common. Total joint replacement can yield persistent pain relief with complete functional recovery in patients with severe ochronotic arthropathy.</p>","PeriodicalId":7018,"journal":{"name":"Acta orthopaedica Belgica","volume":"90 3","pages":"567-570"},"PeriodicalIF":0.6000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tribute to Professor André Vincent (1931-2023).\",\"authors\":\"O Cornu, T Schubert, X Libouton, K Tribak, D Putineanu, M VAN Cauter, L Kaminski, E Thienpont, P-L Docquier, X Banse, J-E Dubuc, O Barbier\",\"doi\":\"10.52628/90.3.12751\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Alkaptonuria (AKU) is an extremely rare autosomal recessive metabolic disorder caused by deficiency of homogentisic acid oxidase and resulting in accumulation of homogentisic acid in collagenous structures. It is characterized by a triad of homogentisic aciduria, bluish-black discoloration of connective tissues (ochronosis) and arthropathy of large weight bearing joints. We report on a middle-aged female patient with bilateral severe ochronotic arthritis of both hips and shoulder joints requiring total joint replacements as staged procedures which were done without complications offering a complete pain relief and a satisfactory clinical and functional outcome. Ochronosis can cause severe arthropathy of peripheral joints. Multiple joint affection is common. Total joint replacement can yield persistent pain relief with complete functional recovery in patients with severe ochronotic arthropathy.</p>\",\"PeriodicalId\":7018,\"journal\":{\"name\":\"Acta orthopaedica Belgica\",\"volume\":\"90 3\",\"pages\":\"567-570\"},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta orthopaedica Belgica\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.52628/90.3.12751\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ORTHOPEDICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta orthopaedica Belgica","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.52628/90.3.12751","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 0

摘要

Alkaptonuria (AKU)是一种极其罕见的常染色体隐性代谢疾病,由均质酸氧化酶缺乏引起,导致均质酸在胶原结构中积累。它的特征是均质性酸尿,结缔组织蓝黑色变色(慢性疾病)和大负重关节的关节病。我们报告一位患有双侧髋关节和肩关节严重慢性关节炎的中年女性患者,要求分阶段进行全关节置换术,无并发症,完全缓解疼痛,临床和功能结果令人满意。衰老可引起周围关节的严重关节病。多重共同情感是常见的。全关节置换术可使严重慢性关节病患者的疼痛持续缓解,功能完全恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Tribute to Professor André Vincent (1931-2023).

Alkaptonuria (AKU) is an extremely rare autosomal recessive metabolic disorder caused by deficiency of homogentisic acid oxidase and resulting in accumulation of homogentisic acid in collagenous structures. It is characterized by a triad of homogentisic aciduria, bluish-black discoloration of connective tissues (ochronosis) and arthropathy of large weight bearing joints. We report on a middle-aged female patient with bilateral severe ochronotic arthritis of both hips and shoulder joints requiring total joint replacements as staged procedures which were done without complications offering a complete pain relief and a satisfactory clinical and functional outcome. Ochronosis can cause severe arthropathy of peripheral joints. Multiple joint affection is common. Total joint replacement can yield persistent pain relief with complete functional recovery in patients with severe ochronotic arthropathy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Acta orthopaedica Belgica
Acta orthopaedica Belgica 医学-整形外科
CiteScore
0.70
自引率
0.00%
发文量
58
审稿时长
4-8 weeks
期刊介绍: Information not localized
期刊最新文献
Limb Salvage in Infected Tibial Nonunion with Bone Loss: A Case Report of a Modified Masquelet-Ilizarov Technique. Diaphyseal intramedullary osteoid osteoma: an enigmatic subtype. Is Severe Knee Osteoarthritis Associated with Intertrochanteric Rather Than Femoral Neck Hip Fractures? Efficacy of Antibiotic-Coated Intramedullary Nails for Septic Shaft Nonunion: Surgical Technique and Outcomes. Solitary Fibrous Tumor Developing Two Years After Primary Cranial Synovial Sarcoma: A Rare Case.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1