Morales Luis C, Alvarado Fernando, Corredor José A, Rodríguez Andrés
Hospital Universitario Fundación Santa Fe de Bogotá, cirugía de Columna, Carrera 7 No. 117-15, Bogotá, DC, Colombia.
Hospital Universitario Fundación Santa Fe de Bogotá, cirugía de Columna, Carrera 7 No. 117-15, Bogotá, DC, Colombia.
Spine J. 2016 Dec;16(12):e755-e760. doi: 10.1016/j.spinee.2016.08.016. Epub 2016 Sep 23.
Many etiologies can lead to atlantoaxial subluxaion. In Grisel syndrome (GS), this subluxation occurs spontaneously after inflammatory processes of the head and neck. Diagnosis is typically based on clinical history and a strong suspicion of this syndrome. Nonsurgical treatment most often resolves the symptoms; however, in some cases surgical treatment is necessary to repair the subluxation. Various surgical techniques and instrumentation systems have been used to treat atlantoaxial subluxation, although there is no consensus regarding the best treatment method for the pediatric population.
To describe a case of atlantoaxial subluxation in a child with GS treated surgically with an alternative construct.
STUDY DESIGN/SETTING: This is a case report and literature review.
Our case study involves a 5-year-old girl with a 6-month history of unresolved Fielding type II atlantoaxial subluxation caused by GS. Despite conservative treatment, the patient's symptoms continued to progress. After two failed closed reduction attempts, open reduction and C1-C2 fusion were performed with atlas laminar hook and axis pedicle polyaxial screws. A literature review of the surgical treatment of GS was also performed.
After surgery, the patient exhibited full clinical and functional recovery with complete resolution of symptoms. At the 36-month follow-up examination, there was continual evidence of satisfactory reduction and fusion. No complications were observed. Upon completion of the literature review, eight GS cases were found to have been treated surgically with the minimum patient age being 9 years.
Conservative management of GS is the most common and effective treatment; however, a few surgical cases have been reported in the literature with good results. Satisfactory clinical results and fusion at 36 months post surgery were seen in a pediatric patient with atlantoaxial subluxation and instability using atlas laminar hook and axis pedicle polyaxial screws.
多种病因可导致寰枢椎半脱位。在格里斯尔综合征(GS)中,这种半脱位发生于头颈部炎症过程之后,且为自发性。诊断通常基于临床病史及对该综合征的高度怀疑。非手术治疗大多能缓解症状;然而,在某些情况下,需要手术治疗来修复半脱位。尽管对于儿科患者的最佳治疗方法尚无共识,但已采用多种手术技术和器械系统来治疗寰枢椎半脱位。
描述1例采用替代结构进行手术治疗的GS患儿寰枢椎半脱位病例。
研究设计/背景:这是1例病例报告及文献综述。
我们的病例研究涉及1名5岁女童,因GS导致的菲尔德ing II型寰枢椎半脱位病史长达6个月。尽管进行了保守治疗,但患者症状仍持续进展。在两次闭合复位尝试失败后,采用寰椎椎板钩和枢椎椎弓根多轴螺钉进行切开复位及C1 - C2融合术。同时还对GS的手术治疗进行了文献综述。
术后,患者临床及功能完全恢复,症状完全消失。在36个月的随访检查中,持续显示复位及融合效果满意,未观察到并发症。完成文献综述后,发现有8例GS病例接受了手术治疗,最小患者年龄为9岁。
GS的保守治疗是最常见且有效的治疗方法;然而,文献中也报道了一些手术病例,效果良好。1例患有寰枢椎半脱位及不稳定的儿科患者,采用寰椎椎板钩和枢椎椎弓根多轴螺钉治疗,术后36个月临床效果满意且实现了融合。