Crossman John E, David Karoly, Hayward Richard, Crockard H Alan
Department of Surgical Neurology, National Hospital for Neurology and Neurosurgery, London, United Kingdom.
J Neurosurg. 2004 Mar;100(3 Suppl Spine):235-40. doi: 10.3171/spi.2004.100.3.0235.
Atlantoaxial rotatory fixation (AARF) is an uncommon disorder of childhood in which resolution usually occurs spontaneously or after traction therapy. In a minority of children irreducible or chronic fixation develop, and the natural history then usually involves restriction of head on neck movement, abnormal head position, and progressive facial asymmetry. The conventional management in these cases has been a posterior fusion.
The authors performed an open reduction via the extreme-lateral approach without adjunctive fixation surgery in 13 children who ranged in age from 4 to 11 years. Postoperatively, halo jacket therapy was undertaken for 8 to 12 weeks. There were no neurological complications despite damage to one vertebral artery and one wound infection. Functional outcome was assessed after a minimum of 24 months (range 29-72 months). Facial asymmetry markedly improved. Sagittal movements were similar to those observed in control individuals. Axial rotation, although reduced compared with that in controls, was present but usually asymmetrical.
In the authors' opinion, open reduction provides the best possibility of normal facial development and return of axial movement in cases of AARF.
寰枢椎旋转固定(AARF)是一种儿童期罕见疾病,通常可自发缓解或经牵引治疗后缓解。少数儿童会出现不可复位或慢性固定,其自然病程通常包括颈部活动时头部受限、异常头位以及进行性面部不对称。这些病例的传统治疗方法是后路融合术。
作者采用经外侧极入路对13例年龄在4至11岁的儿童进行了切开复位,未进行辅助固定手术。术后,采用头环背心治疗8至12周。尽管有1例椎动脉损伤和1例伤口感染,但未出现神经并发症。至少随访24个月(范围29 - 72个月)后评估功能结果。面部不对称明显改善。矢状面活动与对照组相似。轴向旋转虽然比对照组减少,但仍存在且通常不对称。
作者认为,切开复位为AARF病例中面部正常发育和轴向活动恢复提供了最佳可能性。