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一名10岁男孩因多发性颈椎神经纤维瘤导致四肢瘫痪。

Quadriplegia in a 10 year-old boy due to multiple cervical neurofibromas.

作者信息

Garg Sumeet, Hosalkar Harish, Dormans John P

机构信息

Division of Orthopaedic Surgery, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.

出版信息

Spine (Phila Pa 1976). 2003 Sep 1;28(17):E339-43. doi: 10.1097/01.BRS.0000090502.74607.D9.

Abstract

STUDY DESIGN

A case report of a child with quadriplegia as a result of neurofibromatosis type I who had cervical laminectomy for spinal cord decompression followed by occipitocervical instrumentation is described.

OBJECTIVES

To describe the consequences of severe neurofibromatosis type I and an effective surgical technique of occipitocervical instrumentation.

SUMMARY OF BACKGROUND DATA

Neurofibromatosis type I is one of the most commonly inherited genetic disorders in the human population. Extensive intraspinal involvement by neurofibromas can cause significant distortion of normal spinal structure as well spinal cord compression. Extensive laminectomy (with subsequent risk of postsurgical kyphosis) is often required for adequate decompression of the spinal cord.

METHODS

The clinical and radiographic presentation of a child with severe neurofibromatosis type I resulting in quadriplegia is described. The severe neurologic deficit was caused by compression of the spinal cord by intraspinal neurofibromas. Extensive laminectomy was required to adequately decompress the spinal cord. Occipitocervical fusion from the occiput to C6 was done to stabilize the spine and prevent future kyphosis.

RESULTS

Decompression of the spinal cord led to complete neurologic recovery, and instrumentation of the cervical spine was successful in preventing the development of postlaminectomy kyphosis in this pediatric patient.

CONCLUSIONS

The reported case emphasizes the need for treating acute neurologic symptoms caused by spinal cord compression in neurofibromatosis type I as well as addressing the future risk of spinal deformity following laminectomy.

摘要

研究设计

描述了一例因I型神经纤维瘤病导致四肢瘫痪的儿童病例,该患儿接受了颈椎椎板切除术以进行脊髓减压,随后进行了枕颈固定术。

目的

描述严重I型神经纤维瘤病的后果以及枕颈固定术的有效手术技术。

背景资料总结

I型神经纤维瘤病是人类最常见的遗传性疾病之一。神经纤维瘤广泛累及椎管内可导致正常脊柱结构严重变形以及脊髓受压。为充分减压脊髓,常需进行广泛的椎板切除术(随后有术后脊柱后凸的风险)。

方法

描述了一名因严重I型神经纤维瘤病导致四肢瘫痪的儿童的临床和影像学表现。严重的神经功能缺损是由椎管内神经纤维瘤压迫脊髓所致。需要进行广泛的椎板切除术以充分减压脊髓。进行了从枕骨到C6的枕颈融合术以稳定脊柱并防止未来脊柱后凸。

结果

脊髓减压导致神经功能完全恢复,颈椎固定术成功地防止了该小儿患者术后椎板切除术后脊柱后凸的发生。

结论

该报告病例强调了治疗I型神经纤维瘤病中脊髓压迫引起的急性神经症状以及应对椎板切除术后脊柱畸形未来风险的必要性。

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