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影响颅颈区域的特定疾病:成骨不全及相关骨软骨发育不良:基底凹陷的医学与外科治疗

Specific entities affecting the craniocervical region: osteogenesis imperfecta and related osteochondrodysplasias: medical and surgical management of basilar impression.

作者信息

Menezes Arnold H

机构信息

Department of Neurosurgery, University of Iowa Hospitals and Clinics, 200 Hawkins Drive, 1824 JPP, Iowa City, IA 52242, USA.

出版信息

Childs Nerv Syst. 2008 Oct;24(10):1169-72. doi: 10.1007/s00381-008-0602-z. Epub 2008 Apr 10.

DOI:10.1007/s00381-008-0602-z
PMID:18401562
Abstract

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.

摘要

引言

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。

临床资料与方法

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

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

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。

结论

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。

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本文引用的文献

1
Cranio-skeletal dysplasia.颅骨骼发育异常
Br J Radiol. 1948 Jan;21(241):42-8. doi: 10.1259/0007-1285-21-241-42.
2
Osteogenesis imperfecta.成骨不全症
J Neurosurg. 2006 Sep;105(3):359; discussion 359-60. doi: 10.3171/jns.2006.105.3.359.
3
ACRO-OSTEOLYSIS.肢端骨质溶解
Asian J Neurosurg. 2022 Dec 14;17(4):568-576. doi: 10.1055/s-0042-1758843. eCollection 2022 Dec.
4
Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls.软骨-毛发发育不全的颅面和颅颈特征:17 例患者和 34 例对照的影像学研究。
Front Endocrinol (Lausanne). 2021 Dec 10;12:741548. doi: 10.3389/fendo.2021.741548. eCollection 2021.
5
Osteogenesis Imperfecta: Mechanisms and Signaling Pathways Connecting Classical and Rare OI Types.成骨不全症:连接经典型和罕见型 OI 类型的机制和信号通路。
Endocr Rev. 2022 Jan 12;43(1):61-90. doi: 10.1210/endrev/bnab017.
6
Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research.成骨不全症:临床与转化研究的新视角
JBMR Plus. 2019 Feb 20;3(8):e10174. doi: 10.1002/jbm4.10174. eCollection 2019 Aug.
7
Complex spine deformities in young patients with severe osteogenesis imperfecta: current concepts review.重度成骨不全症年轻患者的复杂脊柱畸形:当前概念综述
J Child Orthop. 2019 Feb 1;13(1):22-32. doi: 10.1302/1863-2548.13.180185.
8
Cervical medullary syndrome secondary to craniocervical instability and ventral brainstem compression in hereditary hypermobility connective tissue disorders: 5-year follow-up after craniocervical reduction, fusion, and stabilization.颈椎髓性综合征继发于颅颈不稳定和遗传性过度活动结缔组织疾病的脑干腹侧压迫:颅颈减压、融合和稳定术后 5 年随访。
Neurosurg Rev. 2019 Dec;42(4):915-936. doi: 10.1007/s10143-018-01070-4. Epub 2019 Jan 9.
9
Incorporating the patient perspective in the study of rare bone disease: insights from the osteogenesis imperfecta community.将患者视角纳入罕见骨病研究中:来自成骨不全症社区的见解。
Osteoporos Int. 2019 Feb;30(2):507-511. doi: 10.1007/s00198-018-4690-7. Epub 2018 Sep 6.
10
The Role of the Craniocervical Junction in Craniospinal Hydrodynamics and Neurodegenerative Conditions.颅颈交界区在颅脊流体动力学和神经退行性疾病中的作用。
Neurol Res Int. 2015;2015:794829. doi: 10.1155/2015/794829. Epub 2015 Nov 30.
Am J Roentgenol Radium Ther Nucl Med. 1965 Jul;94:595-607.
4
Hajdu-Cheney syndrome and syringomyelia. Case report.哈伊杜-切尼综合征与脊髓空洞症。病例报告。
J Neurosurg. 2002 Dec;97(6):1441-6. doi: 10.3171/jns.2002.97.6.1441.
5
Hajdu--Cheney syndrome: evolution of phenotype and clinical problems.哈伊杜-切尼综合征:表型演变与临床问题
Am J Med Genet. 2001 May 15;100(4):292-310. doi: 10.1002/1096-8628(20010515)100:4<292::aid-ajmg1308>3.0.co;2-4.
6
Basilar invagination in osteogenesis imperfecta and related osteochondrodysplasias: medical and surgical management.成骨不全及相关骨软骨发育不良中的颅底凹陷:内科及外科治疗
J Neurosurg. 1997 Jun;86(6):950-60. doi: 10.3171/jns.1997.86.6.0950.
7
Causes of death in osteogenesis imperfecta.成骨不全症的死亡原因。
J Clin Pathol. 1996 Aug;49(8):627-30. doi: 10.1136/jcp.49.8.627.
8
Syringomyelia with basilar impression in osteogenesis imperfecta.成骨不全合并基底凹陷的脊髓空洞症。
Acta Neurochir (Wien). 1996;138(7):888-9. doi: 10.1007/BF01411270.
9
Syringomyelia associated with Hajdu-Cheney syndrome: case report.与哈伊杜-切尼综合征相关的脊髓空洞症:病例报告
Neurosurgery. 1996 Aug;39(2):400-3. doi: 10.1097/00006123-199608000-00037.
10
Etiology and pathogenesis of heritable connective tissue diseases.遗传性结缔组织疾病的病因与发病机制。
J Pediatr Orthop. 1993 May-Jun;13(3):392-403. doi: 10.1097/01241398-199305000-00023.