Congenital Mallet Finger: A Case Report

Q3 Medicine
Journal of Hand Surgery Global Online Pub Date : 2026-01-01 Epub Date: 2025-08-05 DOI:10.1016/j.jhsg.2024.11.015
Ricardo Kaempf de Oliveira MD , Paula Fischer MD , Sergi Barrera-Ochoa MD , Pedro J. Delgado MD
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引用次数: 0

Abstract

This study describes a rare case of congenital hypoplasia of the terminal extensor tendon in the fifth finger, resulting in a mallet finger-like deformity, and presents the surgical technique used to correct the deformity. The case involves a three-year-old girl with a flexion deformity of the distal interphalangeal joint of the left fifth finger. Initial conservative treatment was unsuccessful, leading to surgical intervention, which involved resecting the hypoplastic portion of the extensor tendon and directly suturing the healthy proximal and distal portions. The surgery was reinforced with a periosteal strip from the middle phalanx. Postoperative recovery was monitored with physical therapy, and the patient showed successful correction of the deformity after 12 months. There was no recurrence of the deformity or functional limitations. The surgical technique proved effective in resolving the deformity, restoring function, and providing an excellent cosmetic result.
先天性槌状指1例
本研究描述了一例罕见的先天性五指伸肌腱末梢发育不全,导致锤状指样畸形,并介绍了用于纠正畸形的手术技术。该病例涉及一名三岁女孩,左无名指远端指间关节屈曲畸形。最初的保守治疗不成功,导致手术干预,包括切除伸肌腱发育不良的部分,直接缝合健康的近端和远端部分。手术用中指骨骨膜条加固。通过物理治疗监测术后恢复情况,12个月后患者成功矫正了畸形。没有畸形复发或功能限制。手术技术被证明是有效的解决畸形,恢复功能,并提供了良好的美容效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
111
审稿时长
12 weeks
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