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家族性自主神经功能异常中的脊柱畸形。患病率及支具治疗结果。

Spinal deformity in familial dysautonomia. Prevalence, and results of bracing.

作者信息

Hayek S, Laplaza F J, Axelrod F B, Burke S W

机构信息

Department of Pediatric Orthopaedics, The Hospital for Special Surgery, New York, NY 10021, USA.

出版信息

J Bone Joint Surg Am. 2000 Nov;82(11):1558-62.

PMID:11097444
Abstract

BACKGROUND

Familial dysautonomia (Riley-Day syndrome) is an autosomal recessive disorder primarily affecting individuals of Ashkenazi Jewish extraction. It affects the autonomic, central, and peripheral nervous systems. Spinal deformity (mainly scoliosis) is the most common orthopaedic problem in patients with familial dysautonomia. The objectives of our study were to document the prevalence of spinal deformity in a referral center for familial dysautonomia and to determine the effectiveness of bracing.

METHODS

We performed a retrospective radiographic and clinical study of 123 patients with familial dysautonomia who had survived to the age of twenty years or older.

RESULTS

One hundred and two (83 percent) of the 123 patients had spinal deformity: sixty-nine (56 percent) had scoliosis only, thirty-one (25 percent) had scoliosis as well as kyphosis, and two (2 percent) had kyphosis only. Scoliosis was diagnosed by the age of ten years in sixty-four (52 percent) of the patients. Of the sixty-five patients who were treated with bracing, fifty-eight (89 percent) had progression and twenty-four (37 percent) underwent spinal arthrodesis. No risk factors for the presence or progression of the curves could be found.

CONCLUSIONS

The prevalence of spinal deformity in patients with familial dysautonomia who had lived for at least twenty years was found to be 83 percent. By the age of ten years, 52 percent of the patients had scoliosis and 21 percent had kyphosis with or without scoliosis. Bracing was found to be of limited effectiveness as a definitive treatment for spinal deformity. The curve progressed despite bracing in fifty-eight (89 percent) of sixty-five patients.

摘要

背景

家族性自主神经功能异常(赖利 - 戴综合征)是一种常染色体隐性疾病,主要影响阿什肯纳兹犹太裔个体。它会影响自主神经系统、中枢神经系统和周围神经系统。脊柱畸形(主要是脊柱侧凸)是家族性自主神经功能异常患者中最常见的骨科问题。我们研究的目的是记录一家族性自主神经功能异常转诊中心脊柱畸形的患病率,并确定支具治疗的有效性。

方法

我们对123名年龄在20岁及以上且存活的家族性自主神经功能异常患者进行了回顾性影像学和临床研究。

结果

123名患者中有102名(83%)存在脊柱畸形:69名(56%)仅有脊柱侧凸,31名(25%)既有脊柱侧凸又有后凸,2名(2%)仅有后凸。64名(52%)患者在10岁时被诊断出脊柱侧凸。在接受支具治疗的65名患者中,58名(89%)病情进展,24名(37%)接受了脊柱融合术。未发现与脊柱侧凸的存在或进展相关的危险因素。

结论

在至少存活20年的家族性自主神经功能异常患者中,脊柱畸形的患病率为83%。到10岁时,52%的患者患有脊柱侧凸,21%的患者患有后凸,无论是否伴有脊柱侧凸。支具作为脊柱畸形的最终治疗方法效果有限。在65名患者中,58名(89%)尽管使用了支具,病情仍有进展。

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