Department of Orthopedics, Seattle Children's Hospital and University of Washington, Seattle, Washington, United States.
Department of Orthopedics, University of Washington, Seattle, Washington, United States.
Global Spine J. 2015 Jun;5(3):233-8. doi: 10.1055/s-0035-1549432.
Study Design Case report. Objective We report a case of spontaneous atlantoaxial rotatory fixation (AARF) presenting 9 months after onset in an 11-year-old boy. Methods This is a retrospective case report of spontaneous ankylosis of occiput to C2 following traction, manipulative reduction, and halo immobilization for refractory atlantoaxial rotatory fixation. Results The patient underwent traction followed by close manual reduction and placement of halo immobilization after 6 months of severe spontaneous-onset AARF that had been refractory to chiropractic manipulation and physical therapy. Imaging demonstrated dislocation of the left C1-C2 facet joint and remodeling changes of the C2 superior facet prior to reduction, followed by near complete reduction of the dislocation after manipulation and halo placement. Symptoms and clinical appearance were satisfactorily improved and the halo vest was removed after 3 months. At late follow-up, computed tomography demonstrated complete bony ankylosis of the occiput to C2. The patient was found to be HLA B27-positive, but he had no family history of ankylosing spondyloarthropathy or other joint symptoms. The underlying reasons for spontaneous fusion of the occiput to C2 could include the traction, HLA-B27-related spondyloarthropathy, or arthropathic changes caused by traction, reduction, the inciting insult, or immobilization. Conclusion When discussing treatment of childhood refractory AARF by traction, closed manipulation, and halo immobilization, the possibility of developing "spontaneous" ankylosis needs to be considered.
病例报告。目的:我们报告一例 11 岁男孩在发病后 9 个月出现自发性寰枢椎旋转固定(AARF)的病例。方法:这是一例回顾性病例报告,涉及在牵引、手法复位和 halo 固定治疗难治性寰枢椎旋转固定后,枕骨至 C2 自发性粘连的病例。结果:患者在严重的自发性 AARF 发作 6 个月后,经过牵引、闭合手法复位和 halo 固定治疗,该患者对整脊手法和物理治疗均有抵抗。影像学显示左侧 C1-C2 关节突关节脱位和 C2 上关节突重塑改变,复位前,复位后关节突脱位明显改善,随后进行 halo 固定。症状和临床外观得到明显改善, halo 背心 3 个月后移除。在晚期随访时,CT 显示枕骨至 C2 完全骨性融合。患者 HLA B27 阳性,但无强直性脊柱炎或其他关节症状家族史。枕骨至 C2 自发性融合的潜在原因可能包括牵引、HLA-B27 相关的脊柱关节病、或由牵引、复位、激发性损伤或固定引起的关节病变。结论:在讨论通过牵引、闭合手法复位和 halo 固定治疗儿童难治性 AARF 时,需要考虑到“自发性”融合的可能性。