Suppr超能文献

肘部发育性关节强直的病因分类。

An aetiological classification for developmental synostoses at the elbow.

作者信息

McIntyre James D, Benson Michael K D

机构信息

Nuffield Orthopaedic Center, Oxford, UK.

出版信息

J Pediatr Orthop B. 2002 Oct;11(4):313-9. doi: 10.1097/00009957-200210000-00009.

Abstract

Synostoses at the elbow joint are rare. The literature divides them into three groups based on the nature of bony ankylosis; the commonest are humeroradial synostoses. Approximately 150 cases have been reported. There are 29 reported cases of humeroradioulnar synostosis and five of humeroulnar synostosis. An anatomical classification was previously described for humeroradial synostoses. Due to significant phenotypic variability we believe a classification based solely on anatomical characteristics will in some cases be misleading. No classification exists for humeroradioulnar and humeroulnar synostosis. By re-examining the literature we have produced a combined classification for all elbow synostoses which more accurately predicts causes. Congenital elbow synostoses often cause little functional disability. Treatment by soft tissue release and osteotomy has been attempted, but although range of movement is initially, improved re-ossification is the norm. Investigation is more complicated and may be helped by classification which identifies syndrome association, risk of organ anomaly, and inheritance pattern.

摘要

肘关节融合罕见。文献根据骨融合的性质将其分为三组;最常见的是肱桡关节融合。已报道约150例。有29例肱桡尺关节融合和5例肱尺关节融合的报道。先前已对肱桡关节融合进行了解剖学分类。由于显著的表型变异性,我们认为仅基于解剖特征的分类在某些情况下会产生误导。目前尚无肱桡尺关节和肱尺关节融合的分类。通过重新审视文献,我们为所有肘关节融合制定了一种综合分类,能更准确地预测病因。先天性肘关节融合通常很少导致功能残疾。已尝试通过软组织松解和截骨术进行治疗,但尽管最初活动范围有所改善,但重新骨化是常态。检查更为复杂,而识别综合征关联、器官异常风险和遗传模式的分类可能会有所帮助。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验