Rajion Zainul A, Townsend Grant C, Netherway David J, Anderson Peter J, Yusof Asilah, Hughes Toby, Shuaib Ibrahim L, Halim Ahmad Sukari, Samsudin Abdul Rani, David David J
School of Dental Sciences, Universiti Sains Malaysia, Kelantan, Malaysia.
Cleft Palate Craniofac J. 2006 Sep;43(5):513-8. doi: 10.1597/05-023.
To investigate anatomical variations and abnormalities of cervical spine morphology in unoperated infants with cleft lip and palate.
Retrospective cross-sectional investigation of infants born with nonsyndromic cleft lip and palate using computed tomography scans acquired for investigation of a spectrum of clinical conditions.
Computed tomography scan data were obtained from 29 unoperated cleft lip and palate infants and 12 noncleft infants of Malay origin, ages 0 to 12 months.
Observational study of cervical spine computed tomography scans. Heights of cervical vertebral bodies (C2-C7) and intervertebral spaces were measured from landmarks identified from computed tomography reformats and three-dimensional computed tomography reconstructions. Linear modeling of heights and spaces, with age as a covariate, was undertaken to identify differences between the samples.
Anomalous features observed in the cleft lip and palate sample included short posterior arch of C1 (2/29), abnormal development of the anterior arch of C1 (2/29), and fusions of the posterior arch of C2 and C3 (2/29). No anomalies of the cervical spine were observed in the noncleft sample. Although the heights of three cervical vertebral bodies were significantly smaller and two intervertebral spaces were significantly larger in infants with cleft lip and palate compared with noncleft infants (p < .05), overall length of the cervical spine did not differ significantly between the samples.
There was evidence for subtle upper spinal anomalies in the infant cleft lip and palate population. Our finding of reduced size of some cervical vertebral bodies may reflect delayed upper spinal development in infants with cleft lip and palate.
研究未经手术治疗的唇腭裂婴儿颈椎形态的解剖变异和异常情况。
对非综合征性唇腭裂婴儿进行回顾性横断面研究,使用为一系列临床病症检查而获取的计算机断层扫描。
计算机断层扫描数据来自29名未经手术治疗的唇腭裂婴儿以及12名马来族裔、年龄在0至12个月的非唇腭裂婴儿。
对颈椎计算机断层扫描进行观察性研究。从计算机断层扫描重新格式化图像和三维计算机断层扫描重建图像中识别出的标志点测量颈椎椎体(C2 - C7)的高度和椎间隙。以年龄作为协变量对高度和间隙进行线性建模,以确定样本之间的差异。
在唇腭裂样本中观察到的异常特征包括C1后弓短小(2/29)、C1前弓发育异常(2/29)以及C2和C3后弓融合(2/29)。在非唇腭裂样本中未观察到颈椎异常。尽管与非唇腭裂婴儿相比,唇腭裂婴儿的三个颈椎椎体高度明显更小,两个椎间隙明显更大(p < .05),但样本之间颈椎的总长度没有显著差异。
有证据表明唇腭裂婴儿群体存在细微的上颈椎异常。我们发现一些颈椎椎体尺寸减小可能反映了唇腭裂婴儿上颈椎发育延迟。