Operative treatment of congenital pseudarthrosis of the clavicle: a single-centre experience

K. Studer, M. Baker, A. Krieg
{"title":"Operative treatment of congenital pseudarthrosis of the clavicle: a single-centre experience","authors":"K. Studer, M. Baker, A. Krieg","doi":"10.1097/BPB.0000000000000400","DOIUrl":null,"url":null,"abstract":"Congenital pseudarthrosis of the clavicle (CPC) is a very rare condition with a predilection for the right clavicle. Young children are often only symptomatic with activities and as they grow. Operative management in an asymptomatic child is debatable, with various techniques reported in the literature. This is a retrospective, single-centre case series study. All children with CPC treated surgically by resection, bone grafting (nonvascular iliac crest) and plate fixation between 2004 and 2012 at our centre were included. Excluded conditions were traumatic or obstetric fractures of the clavicle, children with musculoskeletal or neurological disorders and children lost to follow-up. Clinical and radiological examination was performed at 6 weeks, 3 months and between 6 and 12 months postoperatively. A total of eight clavicles in seven children (four girls and three boys), with a mean age of 7.1 years (5–8 years), were operated with a mean follow-up of 7 years (4–10 years). In six children, the right (dominant) side was affected, with one child affected bilaterally. Overall, 85% of our patients showed good functional results 6 weeks postoperatively and complete radiographic consolidation at a mean of 8.5 months (3–25 months) postoperatively. One female child showed delayed union, but without clinical deficit. There was low donor-site morbidity. We recommend early operative treatment of CPC with a nonvascularized bone graft from the iliac crest and plate fixation. Level of Evidence: IV.","PeriodicalId":16709,"journal":{"name":"Journal of Pediatric Orthopaedics B","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Orthopaedics B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/BPB.0000000000000400","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15

Abstract

Congenital pseudarthrosis of the clavicle (CPC) is a very rare condition with a predilection for the right clavicle. Young children are often only symptomatic with activities and as they grow. Operative management in an asymptomatic child is debatable, with various techniques reported in the literature. This is a retrospective, single-centre case series study. All children with CPC treated surgically by resection, bone grafting (nonvascular iliac crest) and plate fixation between 2004 and 2012 at our centre were included. Excluded conditions were traumatic or obstetric fractures of the clavicle, children with musculoskeletal or neurological disorders and children lost to follow-up. Clinical and radiological examination was performed at 6 weeks, 3 months and between 6 and 12 months postoperatively. A total of eight clavicles in seven children (four girls and three boys), with a mean age of 7.1 years (5–8 years), were operated with a mean follow-up of 7 years (4–10 years). In six children, the right (dominant) side was affected, with one child affected bilaterally. Overall, 85% of our patients showed good functional results 6 weeks postoperatively and complete radiographic consolidation at a mean of 8.5 months (3–25 months) postoperatively. One female child showed delayed union, but without clinical deficit. There was low donor-site morbidity. We recommend early operative treatment of CPC with a nonvascularized bone graft from the iliac crest and plate fixation. Level of Evidence: IV.
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
先天性锁骨假关节的手术治疗:单中心经验
摘要先天性锁骨假关节(CPC)是一种非常罕见的疾病,主要发生在右侧锁骨。幼儿通常只有在活动和成长过程中才会出现症状。无症状儿童的手术治疗是有争议的,文献中报道了各种技术。这是一项回顾性的单中心病例系列研究。本中心2004年至2012年间通过手术切除、植骨(无血管髂骨)和钢板固定治疗的所有CPC患儿纳入研究。排除的条件是外伤性或产科锁骨骨折,患有肌肉骨骼或神经疾病的儿童以及未随访的儿童。分别于术后6周、3个月及6 ~ 12个月进行临床及影像学检查。7例儿童(4女3男)共8根锁骨,平均年龄5 ~ 8岁,共7.1岁,平均随访7年4 ~ 10年。6例患儿右侧(主侧)受累,1例患儿双侧受累。总体而言,85%的患者在术后6周表现出良好的功能结果,平均在术后8.5个月(3-25个月)完成影像学巩固。1名女婴表现为延迟愈合,但无临床缺陷。供体部位发病率低。我们建议采用无血管化髂骨移植物和钢板固定的早期手术治疗CPC。证据等级:四级。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Analysis of risk factors for nonunion in pediatric lateral column lengthening’ by Torrez et al. A comparison of cone beam computed tomography, standard computed tomography, and plain radiographs in the evaluation of medial epicondyle humerus fractures Letter to the editor, concerning Cimen et al.: ‘Percutaneous release for trigger thumb in children under local anesthesia’ Referral patterns to a pediatric orthopedic clinic: pediatric orthopedic surgeons are primary care musculoskeletal medicine physicians Reliability and validity of Vancouver Scar Scale and Withey score after syndactyly release
×
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学术文献互助
Book学术文献互助群
群 号:481959085
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