Camptodactyly.

IF 0.5 Q4 SURGERY Journal of Hand Surgery-Asian-Pacific Volume Pub Date : 2024-12-01 Epub Date: 2024-11-14 DOI:10.1142/S2424835524300032
Takehiko Takagi
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Abstract

Camptodactyly is a congenital difference with flexion contracture of the proximal interphalangeal (PIP) joint. Camptodactyly limited to one finger is believed to be due to an anomaly of the lumbrical muscle that inserts into the flexor digitorum superficialis (FDS) tendon instead of the extensor expansion, whereas multiple finger camptodactyly is believed to be a result of shortage of soft tissues on the flexor surface of the fingers. It is important to differentiate camptodactyly from other causes of extension lag at the PIP joint. It is difficult to obtain good results after the release of flexion contractures in camptodactyly. The main goal of surgery is to prevent progressive contracture with appropriate postoperative therapy using night splinting and stretching. We should strive for a considered approach based on a thorough understanding of the pathophysiology of camptodactyly. Level of Evidence: Level V (Therapeutic).

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凸足
拇指弯曲畸形(Camptodactyly)是一种伴有近端指间关节(PIP)屈曲挛缩的先天性差异。仅限于单指的拇指外翻被认为是由于插入屈指浅肌腱(FDS)而非伸肌扩张的外侧肌肉异常所致,而多指拇指外翻则被认为是手指屈面软组织短缺的结果。重要的是,要将多指外翻与其他导致 PIP 关节伸展滞后的原因区分开来。外翻畸形患者在解除屈曲挛缩后很难获得良好的效果。手术的主要目的是通过夜间夹板和拉伸等适当的术后治疗来防止挛缩的发展。我们应在充分了解外翻畸形病理生理学的基础上,努力采取一种经过深思熟虑的方法。证据等级:五级(治疗)。
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
304
期刊最新文献
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