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Beare-Stevenson 卷发皮肤综合征患儿头颈部手术后寰椎齿状突慢性半脱位和颈脊髓病的影像学表现。

Imaging findings of chronic subluxation of the os odontoideum and cervical myelopathy in a child with Beare-Stevenson cutis gyrata syndrome after surgery to the head and neck.

机构信息

Department of Diagnostic Imaging, KK Women's and Children's Hospital, Singapore.

出版信息

Ann Acad Med Singap. 2009 Sep;38(9):832-4.

Abstract

INTRODUCTION

Although uncommon, fractures of the os odontoideum are known to occur in children under 7 years old, following acute trauma.

CLINICAL PICTURE

We report a case of chronic subluxation of the os odontoideum resulting in cervical myelopathy in a child with Beare-Stevenson cutis gyrata syndrome after surgery to the head and neck.

TREATMENT AND OUTCOME

The patient was initially put in a Halo vest, following which occipital cervical fusion was performed.

CONCLUSION

Subluxations and fractures at the odontoid synchondrosis are rare but should be anticipated in young children with risk factors for instability of the cervical spine.

摘要

简介

尽管不常见,但已知 7 岁以下儿童在急性创伤后会发生齿状突骨折。

临床图片

我们报告了一例 Beare-Stevenson 脑回样皮肤综合征患儿头颈部手术后,由于齿状突慢性半脱位导致颈脊髓病的病例。

治疗和结果

患者最初被置于 Halo 背心,随后进行了枕颈融合术。

结论

齿状突骺板的半脱位和骨折很少见,但对于有颈椎不稳定危险因素的幼儿应予以预期。

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