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强直性脊柱炎患者寰枢椎前脱位和垂直半脱位的两年随访

Two year followup of anterior and vertical atlantoaxial subluxation in ankylosing spondylitis.

作者信息

Ramos-Remus C, Gomez-Vargas A, Hernandez-Chavez A, Gamez-Nava J I, Gonzalez-Lopez L, Russell A S

机构信息

Department of Rheumatology, Hospital de Especialidades del Centro Medico Nacional de Occidente, IMSS, Guadalajara, Mexico.

出版信息

J Rheumatol. 1997 Mar;24(3):507-10.

PMID:9058657
Abstract

OBJECTIVE

To describe the clinical and radiological 2-yr followup of 22 patients with anterior atlantoaxial subluxation (AAS) from a prospective cohort of patients with ankylosing spondylitis.

METHODS

The 2-yr assessment included a structured questionnaire for rheumatologic and neurologic complaints and lateral cervical radiographs in maximal flexion view. Initial and 2-yr radiographs were assessed blind to patient data. The course of anterior AAS was classified as unchanged (< 1 mm), progression (> or = 1 mm) or regression (> or = 1 mm) at 2 yrs compared with baseline. Vertical AAS was classified using the Sakaguchi-Kauppi method. Magnification factor was corrected using the ratio of C3 width.

RESULTS

Anterior AAS was detected in 22 patients at baseline examination. Two patients also had vertical AAS; 86% were male. Mean age was 33 +/- 9 yrs and mean disease duration was 12 +/- 7 yrs. At followup, one patient had died of acquired immunodeficiency syndrome, 3 could not be reached, and 2 had undergone surgical fusion due to severe myelopathy and now showed complete neurological recovery. Of the remaining 16 patients, 7 (32%) showed progression and 9 (41%) showed no change in the C1-odontoid distance. Vertical AAS developed in one patient. After the 2-yr assessment, 3 additional patients had surgical fusion because of notable progression of AAS, despite absence of neurological signs.

CONCLUSION

Anterior AAS progressed in a number of these patients in the 2 yrs following its detection, and with or without neurological signs, surgical management was thought appropriate in a considerable number of them.

摘要

目的

描述22例来自强直性脊柱炎前瞻性队列研究的寰枢椎前脱位(AAS)患者的临床及影像学2年随访情况。

方法

2年评估包括一份针对风湿性和神经性主诉的结构化问卷,以及颈椎最大前屈位的侧位X线片。对初始和2年的X线片进行评估时,不了解患者数据。将2年时与基线相比的寰枢椎前脱位病程分为不变(<1mm)、进展(≥1mm)或退缩(≥1mm)。采用坂口-考皮法对垂直性寰枢椎前脱位进行分类。使用C3宽度的比值校正放大系数。

结果

基线检查时在22例患者中检测到寰枢椎前脱位。2例患者还存在垂直性寰枢椎前脱位;86%为男性。平均年龄为33±9岁,平均病程为12±7年。随访时,1例患者死于获得性免疫缺陷综合征,3例无法联系到,2例因严重脊髓病接受了手术融合,目前神经功能已完全恢复。其余16例患者中,7例(32%)显示C1齿突间距进展,9例(41%)无变化。1例患者出现垂直性寰枢椎前脱位。2年评估后,另有3例患者因寰枢椎前脱位显著进展而接受了手术融合,尽管没有神经体征。

结论

这些患者中的一些在检测到寰枢椎前脱位后的2年里病情进展,无论有无神经体征,相当一部分患者被认为适合进行手术治疗。

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