重度先天性后凸畸形手术矫正的两阶段手术计划:一个技术病例报告

Saeed Sabbaghan, Hasan Ghandhari, E. Ameri, Naveed Nabizadeh, Saba Saberi, Omid Momen
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引用次数: 0

摘要

先天性脊柱后凸是一种不常见的脊柱畸形,它可以发展并引起神经功能障碍。重症病例的治疗是复杂的。矫正后凸有几种手术干预技术,但手术方法的选择完全取决于患者的病情。这篇文章报告了一个14岁的女孩患有严重的先天性后凸,她在2岁时接受了半表皮成形术。去年,她的神经系统开始恶化,并导致截瘫了几个月。为了治疗她,我们对她进行了2期多段脊柱切除术(Schwab 6型)。首先,她接受了前路T12-L1-L2全椎体切除术和脊髓减压。然后,切除T12至L2的后路假体,并与T8至L5的后路内固定融合。但是对于这种严重的畸形,我们建议使用3D规划,方便手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two-Stage Procedure Planning for the Surgical Correction of Severe Congenital Kyphosis: A Technical Case Report
Congenital kyphosis is a less common spinal malformation, which can progress and cause neurological deficits. The treatment of severe cases is complicated. There are several techniques of surgical intervention for the correction of kyphosis, but the selection of surgical methods is entirely dependent on the patient’s condition. This article reports a 14-year-old girl with severe congenital kyphosis, who underwent hemiepiphysiodesis at age 2. Last year, her neurological deterioration began and led to paraplegia over a couple of months. To treat her, we performed 2-stage multi-level vertebral column resection (Schwab type 6). First, she underwent anterior T12-L1-L2 complete corpectomy and cord decompression. Then, the resection of posterior elements from T12 to L2 and posterior fusion with instrumentation from T8 to L5 were performed. However, concerning this kind of severe deformity, we suggest using 3D planning, which facilitates the operation.
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