首页> 外文期刊>Journal of Hand Surgery. American Volume >Congenital flexion deformity of the middle finger and sagittal band hypoplasia.
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Congenital flexion deformity of the middle finger and sagittal band hypoplasia.

机译:先天性中指屈曲畸形和矢状带发育不全。

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PURPOSE: To report a congenital anomaly of the middle finger. METHOD: Nine patients (16 digits) are reported with congenital flexion deformity of the metacarpophalangeal (MCP) joint of the middle finger. Three patients (4 digits) had isolated deformities to the middle finger and in 6 the deformity was part of congenital ulnar drift (CUD) of the hand. Three patients had Freeman-Sheldon syndrome, 2 had nonsyndromic CUD, and 1 had arthrogryposis multiplex congenita. In CUD patients the middle finger had substantially greater flexion deformity of the MCP joint in comparison with other digits. Seven patients were treated surgically and 2 were treated nonsurgically. Five of the surgical patients had bilateral middle finger involvement. RESULTS: During surgery on 12 digits sagittal band hypoplasia of varying degrees was encountered in all patients and in all patients the extensor tendon of the middle finger was underdeveloped and often ulnarly displaced. Longitudinal imbrication of the remnants of the extensor tendon and centralizing the tendon if necessary by radial sagittal band reefing improved MCP joint flexion deformity. CONCLUSIONS: Congenital middle finger-in-palm deformity in our patients was caused by sagittal band and extensor tendon hypoplasia.
机译:目的:报告中指的先天性异常。方法:9例(16位数)患者报告中指的掌指关节(MCP)先天性屈曲畸形。 3例患者(4位数)中指有孤立的畸形,其中6例畸形是手的先天性尺骨漂移(CUD)的一部分。 3例患有Freeman-Sheldon综合征,2例患有非综合征性CUD,1例患有多发性先天性关节炎。在CUD患者中,与其他手指相比,中指的MCP关节屈曲畸形明显更大。 7例患者接受了外科手术治疗,其中2例接受了非手术治疗。五名外科手术患者有双侧中指受累。结果:在所有患者中,均出现12位数的矢状带发育不全,所有患者中指伸肌肌腱发育不全,并常尺骨移位。伸肌腱残余物的纵向振动,并在必要时通过径向矢状带收束使肌腱居中,从而改善了MCP关节屈曲畸形。结论:我们患者的先天性中指掌畸形是由矢状带和伸肌腱发育不全引起的。

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