Department of Orthopedics and Trauma, Spine Service, K-Plus, Remigius Krankenhaus Leverkusen, An St. Remigius 26, 51379 Leverkusen, Germany.
Eur Spine J. 2013 Jan;22(1):29-35. doi: 10.1007/s00586-012-2329-5. Epub 2012 May 12.
High-grade C1C2 luxation is a rare pathology. There is no clear evidence as to how to treat this deformity. There is only limited evidence about the different surgical techniques and possible approaches including advantages, disadvantages, and complications.
This is an uncommon case of a 13-year-old child with progressive, tetraplegia due to congenital os odontoideum with translational instability between C1 and C2, and progressive luxation of C2. An irreducible dislocation of the C0/C1 complex caused significant compression at the cervicomedullary junction and neurologic deficit. In this paper we highlight the different types of os odontoideum, a review of existing evidence of surgical correction. We will discuss the different treatment strategies which could be applied and the current solution will be described.
Continuous skeletal traction and translational reduction was achieved by a specially designed halo traction system including continuous skeletal traction in a wheelchair for 6 weeks. The surgical treatment consisted of a posterior only release, translational reduction and posterior instrumentation from C0 to C4 with a Y plate and homologous bone graft. Neurological deficits started to improve during halo traction. After surgery the patient was ambulatory without any assistance and reached a Frankel stage E. Postoperative X-rays and CT scan revealed complete reduction at the C1/C2 level and a decompressed cervicomedullary junction.
Treatment of severe C1C2 luxation is difficult with limited evidence in the literature. The current case shows a successful treatment strategy to reduce the deformity and lists alternative approaches.
高位 C1C2 脱位是一种罕见的病理。目前尚无明确证据表明如何治疗这种畸形。关于不同的手术技术和可能的方法,包括优缺点和并发症,只有有限的证据。
这是一个 13 岁儿童的罕见病例,患有进行性四肢瘫痪,病因是先天性齿状突与 C1 和 C2 之间的平移不稳定以及 C2 的进行性脱位。C0/C1 复合体的不可复位脱位导致颈髓交界处严重受压和神经功能缺损。本文重点介绍了不同类型的齿状突异常,并对现有的手术矫正证据进行了回顾。我们将讨论可应用的不同治疗策略,并描述当前的解决方案。
通过专门设计的 halo 牵引系统实现了持续的骨骼牵引和平移复位,该系统包括在轮椅上持续进行 6 周的骨骼牵引。手术治疗包括后路松解、平移复位和后路从 C0 到 C4 的器械固定,使用 Y 型板和同种异体骨移植。在 halo 牵引期间,神经功能缺损开始改善。手术后,患者无需任何帮助即可行走,达到 Frankel 分级 E。术后 X 线和 CT 扫描显示 C1/C2 水平完全复位,颈髓交界处减压。
严重 C1C2 脱位的治疗困难,文献中证据有限。目前的病例展示了一种成功的治疗策略,可减少畸形,并列出了其他方法。