股骨短缩截骨术治疗先天性髌骨脱位1例报告及文献复习。

Samyabrata Das, P Gopinath Menon, C Sitsabesan
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引用次数: 0

摘要

简介:先天性髌骨脱位是一种非常罕见的膝关节疾病,其特征是出生时髌骨外侧脱位,无法复位。这种疾病影响双膝,并且是一种持续性疾病。骨和软组织异常是这种疾病的病理解剖的一部分。诊断是临床证实的存在髌骨移位后外侧。被忽视的疾病可能导致严重的功能损害和膝关节退行性变化,导致残疾随着时间的推移而增加。通常,手术矫正是推荐的治疗方法。病例报告:一名六岁女童被诊断为先天性双膝髌骨脱位。由于这种疾病,这个孩子不能走路。双膝活动范围70°-130°。随后,孩子不得不接受手术修复双侧下肢的膝关节缺损。描述了患者出现时的病情、手术过程和1年后的临床结果。结论:先天性髌骨脱位是一种罕见的疾病,通常从出生开始发展。虽然在先天性髌骨脱位的情况下,反复铸造和支架治疗受影响膝关节屈曲挛缩是有效的,但重新定位移位的髌骨需要手术干预。为了防止任何可能的问题和疾病的长期后果,必须识别它并尽快进行手术干预以修复畸形。通常,手术矫正是这种先天性疾病的推荐治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Femoral Shortening Osteotomy in Managing Congenital Patellar Dislocation: A Case Report and Review of Literature.

Introduction: Congenital patellar dislocation is a very rare knee disorder characterized by the lateral dislocation of patella from birth, which cannot be reduced. The disorder affects both knees and is a persistent condition. Bony and soft tissue anomalies are part of the pathoanatomy of this disorder. The diagnosis is clinically confirmed by the presence of a patella that is displaced posterolaterally. Neglected ailments may lead to severe functional impairment and degenerative changes in the knee joint, resulting in increasing disability over time. Usually, correction by surgery is the recommended treatment approach.

Case report: A 6-year-old female child was diagnosed with congenital patella dislocation in both knees. The child was unable to walk due to this disorder. The range of movement was 70°-130° in both knees. Subsequently, the child had to undergo surgery to repair the knee defect in bilateral lower limbs. The patient's condition at the time of presentation, the surgical procedure, and clinical outcomes at the end of 1 year has been described.

Conclusion: Congenital dislocation of the patella is an uncommon disease that typically develops from birth. Although repeated casting and braces are effective for treating the flexion contracture of the affected knee in case of congenital patella dislocation, repositioning the displaced patella requires surgical intervention. To prevent any possible problems and long-term consequences of the disease, it is essential to identify it and perform a surgical intervention to repair the deformity as soon as possible. Usually, surgical correction is the recommended treatment approach for this congenital disorder.

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