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经治疗的黏多糖贮积症1型(Hurler综合征)中的胸腰椎后凸畸形。

Thoracolumbar kyphosis in treated mucopolysaccharidosis 1 (Hurler syndrome).

作者信息

Yasin M Naveed, Sacho Raphael, Oxborrow Neil J, Wraith J Ed, Williamson J Bradley, Siddique Irfan

机构信息

From the Royal Manchester Children's Hospital, Manchester, United Kingdom.

出版信息

Spine (Phila Pa 1976). 2014 Mar 1;39(5):381-7. doi: 10.1097/BRS.0000000000000157.

Abstract

STUDY DESIGN

A retrospective radiographical follow-up study of thoracolumbar deformity in 33 children with mucopolysaccharidosis 1 (Hurler syndrome).

OBJECTIVE

To report the severity, natural history, risk factors for progression, and results of intervention for thoracolumbar kyphosis in children with Hurler syndrome.

SUMMARY OF BACKGROUND DATA

Literature on the subject of thoracolumbar kyphosis in Hurler syndrome and its treatment is limited to small case series. The natural history and thus indications for intervention are unknown.

METHODS

Patients who had been treated with bone marrow transplantation and/or enzyme replacement therapy were followed up with erect radiographs of the spine. Mean follow-up period was 3.5 years (range, 2-12 yr). Radiographs were retrieved and analyzed retrospectively. Seven patients underwent varied forms of surgical intervention for progressive deformity, the technique and principles of which are described.

RESULTS

The thoracolumbar kyphosis on initial radiographs obtained at a mean age of 17 months measured 38° (95% confidence interval, 34°-42°). Fifteen of the 33 patients (45%) followed for more than 2 years developed a deformity that made a progression of more than 10°. The magnitude of the initial deformity was predictive of whether the deformity progressed (univariate analysis, P < 0.001). An initial kyphosis angle greater than 45° was predictive of progression of more than 10° with sensitivity of 67% and specificity of 88%. All patients who underwent surgical intervention had sustained improvement in the magnitude of thoracolumbar deformity.

CONCLUSION

Thoracolumbar kyphosis in Hurler syndrome is of variable severity with an average deformity, in our series, of 38° at a mean age of 17 months. Forty-five percent of patients developed progression of greater than 10°. Patients with an initial deformity greater than 45° seemed to be more likely to progress. Surgical interventions in the form of anterior fusion, combined anterior and posterior surgery and use of the vertical expandable prosthetic titanium rib provided good correction.

LEVEL OF EVIDENCE

N/A.

摘要

研究设计

一项对33例黏多糖贮积症1型(Hurler综合征)患儿胸腰椎畸形的回顾性影像学随访研究。

目的

报告Hurler综合征患儿胸腰椎后凸的严重程度、自然病程、进展危险因素以及干预结果。

背景资料总结

关于Hurler综合征胸腰椎后凸及其治疗的文献仅限于小病例系列。其自然病程以及干预指征尚不清楚。

方法

对接受过骨髓移植和/或酶替代治疗的患者进行脊柱直立位X线片随访。平均随访期为3.5年(范围2 - 12年)。回顾性检索并分析X线片。7例患者因进行性畸形接受了不同形式的手术干预,并描述了其技术和原则。

结果

初始X线片上胸腰椎后凸在平均年龄17个月时测量为38°(95%置信区间,34° - 42°)。33例随访超过2年的患者中有15例(45%)出现畸形进展超过10°。初始畸形的严重程度可预测畸形是否进展(单因素分析,P < 0.001)。初始后凸角度大于45°可预测进展超过10°,敏感性为67%,特异性为88%。所有接受手术干预的患者胸腰椎畸形严重程度均持续改善。

结论

Hurler综合征的胸腰椎后凸严重程度各异,在我们的系列研究中,平均年龄17个月时平均畸形为38°。45%的患者畸形进展超过10°。初始畸形大于45°的患者似乎更易进展。前路融合、前后联合手术以及使用垂直可扩张人工钛肋骨等手术干预提供了良好的矫正效果。

证据级别

无。

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