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克鲁宗综合征中的颈椎

The cervical spine in Crouzon syndrome.

作者信息

Anderson P J, Hall C, Evans R D, Harkness W J, Hayward R D, Jones B M

机构信息

Department of Craniofacial Surgery, Great Ormond Street Hospital for Children, London, United Kingdom.

出版信息

Spine (Phila Pa 1976). 1997 Feb 15;22(4):402-5. doi: 10.1097/00007632-199702150-00009.

Abstract

STUDY DESIGN

All cervical spine radiographs of 44 patients with Crouzon syndrome treated at Great Ormond Street Hospital during the past 10 years were studied.

OBJECTIVES

To assess the incidence and pattern of cervical spine abnormalities of patients with a confirmed diagnosis of Crouzon syndrome, but particularly regarding progressive fusion.

SUMMARY OF BACKGROUND DATA

Previous studies into the cervical spine anomalies in those with Crouzon syndrome have shown an increased incidence of congenital abnormalities compared with the normal population. There is some suggestion from previous studies that cervical spine fusions are progressive in nature.

METHODS

All radiographs were reviewed by the craniofacial team, along with a single pediatric radiologist with experience in assessment of skeletal dysplasias.

RESULTS

Radiologic abnormalities included "butterfly" vertebrae and fusions of the bodies and the posterior elements. Evidence of fusion was present in eight of 44 (18%) of patients. C2-C3 and C5-C6 were almost equally affected. Block fusions involving multiple vertebrae were seen. Analysis of sequential studies in 16 patients showed evidence of progression in five.

CONCLUSIONS

These results reveal an incidence of fusions that is lower than reported previously. There is radiologic evidence from serial studies that the fusions are progressive, and because these patients are children, the fusion process may not be complete, which may account for the lower incidence of fusions than in previous studies. The pattern of fusions is different from that in earlier studies, which may be a result of the method of diagnosis because this population is less likely to include atypical forms of other syndromes (which have a higher incidence of cervical fusions, particularly at C2-C3). Regarding other congenital anomalies, it appears that butterfly vertebrae are especially prevalent in association with Crouzon syndrome.

摘要

研究设计

对过去10年在大奥蒙德街医院接受治疗的44例克鲁宗综合征患者的所有颈椎X线片进行研究。

目的

评估确诊为克鲁宗综合征患者颈椎异常的发生率和模式,尤其是关于进行性融合。

背景资料总结

先前对克鲁宗综合征患者颈椎异常的研究表明,与正常人群相比,先天性异常的发生率增加。先前的研究有一些提示,颈椎融合本质上是进行性的。

方法

所有X线片由颅面团队以及一位在评估骨骼发育异常方面有经验的儿科放射科医生进行复查。

结果

放射学异常包括“蝴蝶”椎以及椎体和后部结构的融合。44例患者中有8例(18%)存在融合证据。C2-C3和C5-C6受影响程度几乎相同。可见涉及多个椎体的块状融合。对16例患者的系列研究分析显示,有5例有进展证据。

结论

这些结果显示融合的发生率低于先前报道。系列研究的放射学证据表明融合是进行性的,并且由于这些患者是儿童,融合过程可能未完成,这可能是融合发生率低于先前研究的原因。融合模式与早期研究不同,这可能是诊断方法的结果,因为该人群不太可能包括其他综合征的非典型形式(这些综合征颈椎融合的发生率较高,尤其是在C2-C3)。关于其他先天性异常,似乎蝴蝶椎在克鲁宗综合征中尤其常见。

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