先天性多指屈曲畸形的临床特点及手术表现

T. Ogino, S. Ishii, H. Kato
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引用次数: 1

摘要

摘要将36例先天性多指屈曲畸形分为先天性挛缩型、远端关节挛缩型、Freeman - Sheldon样综合征、先天性指伸肌发育不全型、尺侧漂移型和多发喜指型6种类型。在这些畸形中观察到许多手部常见的临床特征。在11例患者中,18只手接受了手术治疗,随访时间超过一年。在手术中,大多数病例的畸形都得到了完全矫正或显著减少。从这些手术结果来看,我们认为先天性多指屈曲畸形的主要原因是掌部皮肤和皮肤保留韧带的挛缩。随访时,10只手完全矫正,8只手不完全矫正或轻微矫正。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Features and Operative Findings of Congenital Flexion Deformity of Multiple Digits
ABSTRACT Thirty‐six cases with congenital flexion deformities of multiple digits were classified into six types such as congenital contractural arachnodactyly, distal arthrogryposis, Freeman‐Sheldon‐like syndrome, congenital aplasia of the extensor muscles of the digits, ulnar drift type and multiple camptodactyly type. Many common clinical features of the hands were observed among these deformities. In eleven cases, 18 hands were treated surgically and were followed up for more than a year. During surgery, complete correction or signigicant reduction of the deformity was achieved in most cases. From these operative findings, it was assumed that the main cause of congenital flexion deformity of multiple digits was contracture of the palmar skin and retaining ligaments of the skin. At follow up, complete correction was achieved in 10 hands, and incomplete or minimal correction in eight hands.
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