Menezes Arnold H
Department of Neurosurgery, University of Iowa Hospitals and Clinics, 200 Hawkins Drive, 1824 JPP, Iowa City, IA 52242, USA.
Childs Nerv Syst. 2008 Oct;24(10):1169-72. doi: 10.1007/s00381-008-0602-z. Epub 2008 Apr 10.
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.
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 and signs included headache, lower cranial nerve dysfunction, dysphagia, respiratory embarrassment, weakness, and ataxia.
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.
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.
In conclusion, we feel that early intervention with occipitocervical bracing can prevent the progressive march of significant basilar impression which leads to mortality.
成骨不全症(OI)是一种由胶原蛋白合成缺陷引起的遗传性骨发育障碍。随之而来的基底凹陷或继发性基底内陷并不常见,但可能具有毁灭性。
1985年至2005年间,对52例患有基底凹陷的骨软骨发育不良患者(28例成骨不全症、6例哈伊杜-切尼综合征、6例佩吉特病和12例脊椎骨骺发育不良)进行了评估。该队列中的男女比例为1:1。就诊时的平均年龄为12.2岁。
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。
在该系列研究的早期(1985 - 1995年),所有脑积水患者均接受分流手术,并对脑桥延髓交界处的腹侧压迫进行经口腹侧减压,随后进行枕颈背侧融合术。经过此次评估,认为如果存在脑积水,大多数患者在分流后早期进行支具固定会受益。然而,20%的患者仍需要进行前路腹侧减压和枕颈融合术。
结果显示融合稳定,但随着时间推移,成骨不全症患者以及哈伊杜-切尼综合征患者出现了渐进性前屈。所有脊椎骨骺发育不良患者均获得了良好、牢固且稳定的融合,经受住了时间的考验。
总之,我们认为早期进行枕颈支具固定干预可以预防导致死亡的严重基底凹陷的渐进发展。