Kolar John C
Medical City Children's Hospital, Dallas, Texas 75230, USA.
J Craniofac Surg. 2011 Jan;22(1):47-9. doi: 10.1097/SCS.0b013e3181f6c2fb.
To compare our data with recent studies that have suggested a change in the distribution of the forms of nonsyndromal synostosis in the clinical population, we conducted a retrospective analysis of the diagnoses of children with isolated synostosis examined at a large craniofacial center between 1987 and 2009. This also included the range of nonsyndromal multisuture synostoses.
A retrospective chart review of all preoperative patients with nonsyndromal synostosis seen between 1987 and 2009 was performed. Only patients with a radiologically confirmed craniosynostosis were included. Data on patients' sex and laterality in unilateral synostoses were collected. Two temporally distinct subgroups (1996-2000 and 2005-2009) were defined to evaluate changes in the distribution of the most common forms of isolated craniosynostosis using the Fisher exact test.
A total of 690 patients met the inclusion criteria. The largest group of patients had sagittal synostosis, with metopic synostosis as the second most common diagnosis, representing one-fourth of the patients, followed closely by unilateral coronal synostosis. All other synostoses encompassed one-eighth of the group. Patients with sagittal or metopic synostosis were overwhelmingly male, whereas those with unilateral coronal synostosis were predominantly female. Patients with unilateral synostoses were affected primarily at the right suture.
Data from our patients indicate a much higher incidence of metopic synostosis than has been reported in the traditional clinical literature but is consistent with recent published data. The causes of this are unclear at this point, but the Fisher exact test excludes an increase in the frequency of metopic synostosis. Improved clinical diagnosis or ascertainment bias remains a possibility. Further research is needed to elucidate the answer to this question. Our data also indicate the occurrence of a small number of rare multisuture synostoses of unknown origin.
为了将我们的数据与近期研究进行比较,这些研究表明临床人群中非综合征性颅缝早闭的类型分布有所变化,我们对1987年至2009年期间在一家大型颅面中心接受检查的孤立性颅缝早闭患儿的诊断进行了回顾性分析。这也包括非综合征性多缝颅缝早闭的范围。
对1987年至2009年期间所有术前诊断为非综合征性颅缝早闭的患者进行回顾性病历审查。仅纳入经放射学证实的颅缝早闭患者。收集患者的性别和单侧颅缝早闭的患侧数据。定义了两个时间上不同的亚组(1996 - 2000年和2005 - 2009年),使用Fisher精确检验评估孤立性颅缝早闭最常见类型的分布变化。
共有690例患者符合纳入标准。最大的患者组为矢状缝早闭,额缝早闭是第二常见的诊断,占患者总数的四分之一,紧随其后的是单侧冠状缝早闭。所有其他颅缝早闭占该组的八分之一。矢状缝或额缝早闭的患者绝大多数为男性,而单侧冠状缝早闭的患者主要为女性。单侧颅缝早闭的患者主要累及右侧缝。
我们患者的数据表明,额缝早闭的发病率比传统临床文献报道的要高得多,但与近期发表的数据一致。目前尚不清楚其原因,但Fisher精确检验排除了额缝早闭频率增加的可能性。临床诊断的改善或确诊偏倚仍有可能。需要进一步研究以阐明这个问题的答案。我们的数据还表明存在少数来源不明的罕见多缝颅缝早闭。