Humphrey Joel, Wilson-Macdonald James
West Middlesex University Hospital NHS Trust, Twickenham Road, Isleworth, Middlesex, UK.
Eur Spine J. 2009 Jul;18 Suppl 2(Suppl 2):168-71. doi: 10.1007/s00586-008-0754-2. Epub 2008 Sep 2.
This is a case report of a 15-month-old patient with osteogenesis imperfecta (OI) who sustained atlanto-axial dislocation. Our objective is to report a unique case of traumatic atlanto-axial subluxation in a child with osteogenesis imperfecta associated with bilateral femoral fractures. The management is discussed. Atlanto-axial dislocation occurring with associated osteogenesis imperfecta is very rare. There have been no previous reported cases. A 15-month-old girl with osteogenesis imperfecta sustained a traumatic atlanto-axial dislocation. The child was followed-up through presentation, diagnosis, management and post-discharge. The initial diagnosis was confirmed with a CT scan. The patient was treated conservatively with a halo-traction for 4 weeks followed by a halo jacket for a further 4 weeks. Both appliances were fitted under general anaesthetic. An anatomical reduction was achieved. There was no neurological deficit at any stage. The child has had a successful outcome. She is asymptomatic with a full range of movement at the atlanto-axial joints at 9 months. In conclusion, this paper records our management of this rare problem.
这是一例15个月大的成骨不全(OI)患者发生寰枢椎脱位的病例报告。我们的目的是报告一例患有成骨不全且伴有双侧股骨骨折的儿童发生创伤性寰枢椎半脱位的独特病例,并讨论其治疗方法。与成骨不全相关的寰枢椎脱位非常罕见,此前尚无报道病例。一名15个月大的患有成骨不全的女童发生了创伤性寰枢椎脱位。对该患儿进行了从就诊、诊断、治疗到出院后的随访。通过CT扫描确诊了最初的诊断。患者接受了为期4周的头环牵引保守治疗,之后又佩戴头环背心4周。这两种器具均在全身麻醉下安装。实现了解剖复位。在任何阶段均无神经功能缺损。患儿取得了成功的治疗结果。9个月时,她无症状,寰枢椎关节活动范围正常。总之,本文记录了我们对这一罕见问题的治疗过程。