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本文引用的文献

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Skull base abnormalities in osteogenesis imperfecta: a cephalometric evaluation of 54 patients and 108 control volunteers.成骨不全症患者的颅底异常:54例患者和108例对照志愿者的头影测量评估
J Neurosurg. 2006 Sep;105(3):361-70. doi: 10.3171/jns.2006.105.3.361.
2
Treatment of atlantoaxial instability in pediatric patients.小儿寰枢椎不稳的治疗
Neurosurg Focus. 2003 Dec 15;15(6):ECP1. doi: 10.3171/foc.2003.15.6.7.
3
Inflammatory atlanto-axial subluxation (Grisel's syndrome) in children: clinical diagnosis and management.儿童炎性寰枢椎半脱位(格里斯尔综合征):临床诊断与处理
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Current management of pediatric atlantoaxial rotatory subluxation.小儿寰枢椎旋转性半脱位的当前治疗方法。
Spine (Phila Pa 1976). 1998 Oct 15;23(20):2174-9. doi: 10.1097/00007632-199810150-00006.
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Traumatic atlantoaxial rotatory subluxation and dislocation.创伤性寰枢椎旋转半脱位和脱位
Spine (Phila Pa 1976). 1995 Sep 1;20(17):1928-30. doi: 10.1097/00007632-199509000-00016.
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Acute fractures and dislocations of the cervical spine in children and adolescents.
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Acute spinal-cord lesions in a pediatric population: epidemiological and clinical features.
Paraplegia. 1980 Jun;18(3):206-19. doi: 10.1038/sc.1980.36.
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Early diagnosis of atlanto-axial rotatory fixation.寰枢椎旋转固定的早期诊断
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CT-functional diagnostics of the rotatory instability of upper cervical spine. 1. An experimental study on cadavers.
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Instability of the upper cervical spine in Down syndrome.
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一名患有成骨不全症的婴儿发生旋转性寰枢椎脱位。

Rotatory atlanto-axial dislocation in an infant with osteogenesis imperfecta.

作者信息

Humphrey Joel, Wilson-Macdonald James

机构信息

West Middlesex University Hospital NHS Trust, Twickenham Road, Isleworth, Middlesex, UK.

出版信息

Eur Spine J. 2009 Jul;18 Suppl 2(Suppl 2):168-71. doi: 10.1007/s00586-008-0754-2. Epub 2008 Sep 2.

DOI:10.1007/s00586-008-0754-2
PMID:18762995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2899552/
Abstract

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.

摘要

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。