Department of Orthopaedics, Traumatology and Spine Surgery, Ganga Hospital, 313 Mettupalayam Road, Coimbatore 641043, India.
Eur Spine J. 2011 Mar;20(3):343-8. doi: 10.1007/s00586-010-1526-3. Epub 2010 Aug 18.
Childhood spinal tuberculosis, especially when associated with severe vertebral destruction of more than two vertebral bodies can end up in severe deformity. These children show progressive deformity throughout the period of growth and can develop severe kyphosis of >100°. Such kyphosis is severely disabling with significant risk of neurological deficit and respiratory compromise. Surgical correction of these deformities by both anterior and posterior approaches has been described but each have serious limitations of approach, correctability and safety. We describe here a technique of posterior closing-anterior opening osteotomy, which allowed us to correct a rigid post-tubercular deformity of 118° in a 13-year-old boy with neglected spinal tuberculosis. The patient was a 13-year-old boy, who had contracted spinal tuberculosis at the age of 6 years. Although the disease was cured by anti-tubercular chemotherapy, he continued to deteriorate in deformity and presented to us with severe thoracolumbar kyphosis (118°). He was neurologically intact but was beginning to show shortness of breath on exertion. Patient also had fore shortening of the trunk with impingement of the rib cage on the iliac crest. Radiographs revealed complete destruction of T12, L1 and L2 vertebral bodies with the T11 vertebra fusing with L3 anteriorly. CT scans and MRI revealed severe collapse of the vertebral column and the spinal cord being stretched over the 'internal gibbus', which was formed by the remnants of the destroyed vertebrae. A single stage closing-opening osteotomy was done by a midline posterior approach with continuous intraoperative spinal cord monitoring. The procedure involved extensive laminectomy of T11-L2, pedicle screw fixation of three levels above and three levels below the apex, a wedge osteotomy at the apex of the deformity from both sides, anterior column reconstruction by appropriate-sized titanium cage and gradual correction of deformity by closing the posterior column using the cage as a fulcrum. This allowed us to achieve a correction to 38° (68% correction). There was no intraoperative or perioperative adverse event and patient had good functional and radiological outcome at 1-year follow-up. In this Grand Rounds case presentation, we have also discussed the aetiology and evolution of severe post-tubercular kyphosis, which is the most common cause of spinal deformity in the developing world. Early identification of children at risk for severe deformity, the time and ideal methods of prevention of such deformities are discussed. The pros and cons of the available options of surgical correction of established deformity and the merits of our surgical technique are discussed.
儿童期脊柱结核,特别是当累及两个以上椎体的严重椎体破坏时,最终会导致严重畸形。这些儿童在生长过程中会出现进行性畸形,并可能发展为 >100°的严重后凸畸形。这种后凸畸形严重致残,有显著的神经功能缺损和呼吸功能障碍风险。已经描述了通过前后入路进行这些畸形的矫正,但每种方法都存在入路、矫正能力和安全性方面的严重限制。我们在此描述了一种后路闭合-前路撑开截骨术技术,该技术可用于矫正一名患有被忽视的脊柱结核的 13 岁男孩的僵硬性结核后凸畸形。该患者为 13 岁男孩,6 岁时患有脊柱结核。尽管通过抗结核化疗治愈了该病,但他的畸形仍持续恶化,并因严重的胸腰椎后凸畸形(118°)就诊。他的神经功能完整,但开始在用力时出现呼吸急促。患者还出现了躯干前缩短,胸廓肋骨撞击髂嵴。影像学检查显示 T12、L1 和 L2 椎体完全破坏,T11 椎体与 L3 椎体在前方融合。CT 扫描和 MRI 显示脊柱严重塌陷,脊髓被“内部脊柱后凸”(由破坏的椎体残端形成)拉伸。通过后路中线入路进行了一期闭合-撑开截骨术,并持续进行术中脊髓监测。该手术涉及 T11-L2 的广泛椎板切除术、三个以上和三个以下顶点的椎弓根螺钉固定、畸形顶点两侧的楔形截骨、合适大小钛笼的前柱重建和通过使用笼作为支点逐渐矫正后柱来实现畸形矫正。这使得我们能够实现 38°的矫正(68%的矫正率)。术中或围手术期无不良事件发生,患者在 1 年随访时取得了良好的功能和影像学结果。在本次大查房病例介绍中,我们还讨论了严重结核后凸畸形的病因和演变,这是发展中国家最常见的脊柱畸形原因。讨论了早期识别有严重畸形风险的儿童、预防此类畸形的时间和理想方法。讨论了现有的矫正已确立畸形的手术矫正方法的优缺点以及我们的手术技术的优点。