首页> 美国卫生研究院文献>Evidence-Based Spine-Care Journal >Thoracic pedicle subtraction osteotomy in a pediatric patient: a case report
【2h】

Thoracic pedicle subtraction osteotomy in a pediatric patient: a case report

机译:儿科患者胸腰椎蒂减影截骨术1例

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Study design: Case report.>Objective: To describe a case of thoracic pedicle subtraction osteotomy (PSO) for congenital kyphosis in a child.>Background information: Although congenital kyphosis is rare, it is a challenging cause of pediatric myelopathy and frank paralysis. Even less common is the use of PSO for the surgical management of focal congenital kyphosis. We present the case of a child with congenital kyphosis that was managed with a pedicle subtraction osteotomy.>Methods: A detailed history and physical examination were performed with careful review of the patient’s medical records and x-ray studies. A PSO at T11 was performed along with T9 through L1 instrumented posterolateral fusion.>Case description: A 10-year-old girl was evaluated for walking difficulty and a lump on her back. Physical examination revealed a sharp gibbus kyphosis in the lower thoracic spine with tenderness and bilateral back muscle spasms. The patient displayed difficulty with balance lacking a smooth, regular gait rhythm. Clonus and radiculopathy were not present. Plain x-ray of the thoracolumbar spine revealed hyperkyphosis and failure of anterior wall segmentation between T10 and T11 vertebral bodies. Cobb’s angle measured 65 degrees. Due to her symptoms and degree of correction required, we elected to perform a PSO at T11 along with T9 to L1 posterolateral instrumentation fusion. No intraoperative complications occurred. There was a significant improvement in her posture and gait.>Discussion: A thoracic PSO for congenital kyphosis was safely performed with an excellent outcome. To our knowledge, this is the first PSO procedure performed in Uganda.
机译:>研究设计:病例报告。>目的:描述一例儿童先天性后凸畸形的胸椎椎弓根切开截骨术(PSO)。>背景信息:尽管先天性后凸畸形很少见,但它是小儿脊髓病和坦率麻痹的具有挑战性的原因。使用PSO进行局灶性先天性后凸畸形的外科手术治疗更为罕见。我们介绍了一例先天性后凸畸形的儿童,该儿童经椎弓根减影截骨术治疗。>方法:对病史和体格进行了详细检查,并仔细检查了患者的病历和X光检查。通过L1器械后外侧融合术在T11与P9进行PSO。>病例描述:对一名10岁女孩的行走困难和背部肿块进行了评估。体格检查发现下胸椎有明显的吉布斯驼背畸形,伴有压痛和双侧背部肌肉痉挛。患者表现出平衡困难,缺乏平稳,规律的步态节奏。不存在克隆性和神经根病。胸腰椎的X线平片显示T10和T11椎体之间的高度后凸和前壁分割失败。柯布的角度为65度。由于她的症状和所需的矫正程度,我们选择在T11与T9到L1后外侧器械融合进行PSO。术中无并发症发生。她的姿势和步态有明显改善。>讨论:安全地进行了先天性后凸畸形的胸廓PSO手术,效果良好。据我们所知,这是在乌干达执行的第一个PSO程序。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号