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首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Specific entities affecting the craniocervical region : Osteogenesis imperfecta and related osteochondrodysplasias: medical and surgical management of basilar impression.
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Specific entities affecting the craniocervical region : Osteogenesis imperfecta and related osteochondrodysplasias: medical and surgical management of basilar impression.

机译:影响颅颈区域的特定实体:成骨不全症和相关的骨软骨发育不良:基底印象的内科和外科治疗。

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INTRODUCTION: Osteogenesis imperfecta (OI) is an inheritable disorder of bone development caused by defective collagen synthesis. The attendant basilar impression or secondary basilar invagination is uncommon but can be devastating. CLINICAL MATERIALS AND METHODS: Fifty-two patients with osteochondrodysplasia (28 with OI, six with Hajdu-Cheney syndrome, six with Paget's disease, and 12 with spondyloepiphyseal dysplasia) with basilar impression were evaluated between 1985 and 2005. The male/female ratio in this cohort was 1:1. The mean age at presentation was 12.2 years. SYMPTOMS: Symptoms and signs included headache, lower cranial nerve dysfunction, dysphagia, respiratory embarrassment, weakness, and ataxia. TREATMENT: In the earlier part of the series (1985-1995), all patients with hydrocephalus were shunted and a ventral transoral decompression made for ventral compression of the pontomedullary junction followed by a dorsal occipitocervical fusion. As a result of this evaluation, it was felt that most patients would benefit by early bracing after the hydrocephalus was shunted if it existed. However, 20% of patients still required an anterior ventral decompression and the occipitocervical fusion. RESULTS: The results showed that the fusions were stable but over a period of time, there was progressive forward bending with osteogenesis imperfecta as well as with the Hajdu-Cheney syndrome. All patients with spondyloepiphyseal dysplasia had a good strong stable fusion which stood the test of time. CONCLUSION: In conclusion, we feel that early intervention with occipitocervical bracing can prevent the progressive march of significant basilar impression which leads to mortality.
机译:简介:成骨不全症(OI)是由胶原合成缺陷引起的骨发育遗传性疾病。随之而来的基底印象或继发性基底内陷很少见,但可能具有破坏性。临床材料和方法:在1985年至2005年之间评估了52例具有基底印象的骨软骨发育不良的患者(28例OI,6例Hajdu-Cheney综合征,6例Paget病和12例自发性脊柱骨干发育不良)。男女比例这个队列是1:1。报告时的平均年龄为12.2岁。症状:症状和体征包括头痛,下颅神经功能障碍,吞咽困难,呼吸窘迫,虚弱和共济失调。治疗:在该系列的早期部分(1985-1995年),对所有脑积水患者进行分流,并进行腹侧经口减压以压缩椎弓根交界处,然后进行背枕颈融合。作为该评估的结果,认为如果存在脑积水,则大多数患者将在脑积水被分流后通过早期支架受益。但是,仍有20%的患者需要前腹减压和枕颈融合术。结果:结果显示融合稳定,但在一段时间内,成骨不全以及Hajdu-Cheney综合征出现进行性正向弯曲。所有患有脊柱骨赘发育不良的患者均具有良好的牢固稳定融合,经得起时间的考验。结论:总的来说,我们认为采用枕颈撑杆的早期干预可以防止显着的基底印象的进行性行进,从而导致死亡。

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