多重先天性关节挛缩症手部畸形的分型及治疗临床分析

Peng Lu, W. Tian, Jun-hui Zhao, Yang Guo, Yong Yang, Kun Liu, Yaobin Yin, Liying Sun, Wenyao Zhong
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引用次数: 0

摘要

目的探讨多发性先天性关节挛缩症手部畸形的分型及治疗效果。方法对2010年1月~ 2018年1月收治的72例(144只拇指,556只其他手指)先天性多关节挛缩手部畸形患者进行手术治疗。根据患者不同的病理解剖特点分为6组,进行相应的治疗。结果60例患者(拇指93例,其他手指296例)术后随访1 ~ 83个月,平均16.2个月。患指临床疗效总体优良率为87.4%(340/389),其中大拇指为76.3%(71/93),其他手指为90.9%(269/296)。所有植皮均存活,1个手指复发。结论本组患者治疗后手指活动良好,安全性高。因此,根据本文描述的分类方法,对多重先天性关节挛缩的手部畸形患者进行相应的治疗,可以取得良好的效果。关键词:手部畸形;先天性;治疗效果;多发性先天性关节挛缩
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Classification and treatment of hand deformities of arthrogryposis multiplex congenita: a clinical analysis
Objective To explore the classification and treatment efficacy of hand deformities of arthrogryposis multiplex congenita. Methods From January 2010 to January 2018, 72 patients (144 thumbs, 556 other fingers) with hand deformities of arthrogryposis multiplex congenita were treated. The patients were divided into 6 groups according to their different pathological and anatomical characteristics and treated accordingly. Results Postoperatively, 60 patients (93 thumbs, 296 other fingers) were follow-up for 1 to 83 months, with an average of 16.2 months. The overall excellent and good rate of the clinical efficacy of the affected fingers was 87.4% (340/389), of which 76.3% (71/93) was for the thumbs and 90.9% (269/296) for the other fingers. All skin grafts survived and 1 finger recurred. Conclusion All the patients in this group have satisfactory finger movement and high safety after treatment. Therefore, according to the classification method described in this paper, the patients with hand deformities of arthrogryposis multiplex congenita can be treated accordingly, which can achieve good results. Key words: Hand deformities,congenital; Treatment outcome; Arthrogryposis multiplex congenita
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