Department of Neurosurgery, Research Institute of Clinical Medicine, Institute for Medical Sciences, Chonbuk National University Medical School and Hospital, Jeonju, Korea.
Spine (Phila Pa 1976). 2011 Jan 15;36(2):E144-7. doi: 10.1097/BRS.0b013e3181efa320.
case report and review of the literature.
to report on a patient presenting with anteroposterior defects of the arch of the atlas with a rare type of posterior arch defect. This report includes a literature review of the hypothesis for the development of this anomaly.
congenital bony defects of the atlas are uncommon. Isolated posterior clefts are the most frequent anomaly, but combined anterior and posterior defects are the least common. In particular, combined anteroposterior defects of the arch of the atlas with other types of posterior arch defects, not including type A, have not been reported. These anomalies can cause confusion, particularly in the setting of trauma when the radiologic finding may be misinterpreted as representing a fracture.
we report here on a 22-year-old man with an anteroposterior defect of the atlas who complained of neck pain after a traffic accident. The computed tomography demonstrated well-corticated defects with sclerotic changes and no evidence of soft tissue swelling adjacent to the bony discontinuities, consistent with a congenital abnormality. Suspecting anteroposterior spondyloschisis, we performed only conservative treatment.
the patient improved on conservative therapy without a surgical procedure.
we describe combined anteroposterior defects of the arch of the atlas along with other types of posterior arch defects. Most congenital defects of the arch of the atlas are found during radiologic evaluation of neck pain after trauma. Careful diagnosis is needed for these patients to avoid confusing these defects with a fracture.
研究设计:病例报告及文献回顾。
目的:报告一例表现为寰椎弓前后缺损的患者,伴有一种罕见的后弓缺损类型。本报告包括对该异常发育假说的文献回顾。
背景数据概要:寰椎先天性骨缺损并不常见。单纯的后裂是最常见的异常,但前后联合缺损是最少见的。特别是,伴有其他类型后弓缺损的寰椎弓前后联合缺损,不包括 A 型,尚未有报道。这些异常可能会引起混淆,特别是在创伤时,影像学表现可能被误诊为骨折。
方法:我们在此报告一例 22 岁男性,因交通事故后出现颈部疼痛而就诊,表现为寰椎弓前后缺损。计算机断层扫描显示皮质完整的缺损,有硬化改变,在骨不连续处无软组织肿胀的证据,符合先天性异常。考虑到前后脊椎分裂,我们仅进行了保守治疗。
结果:患者在保守治疗后症状改善,无需手术。
结论:我们描述了伴有其他类型后弓缺损的寰椎弓前后联合缺损。大多数寰椎弓先天性缺损是在创伤后颈部疼痛的放射学评估中发现的。对于这些患者,需要仔细诊断,以避免将这些缺损与骨折混淆。