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寰椎发育不全所致颈椎脊髓病及先天性狭窄:三例报告并文献复习

Cervical myelopathy and congenital stenosis from hypoplasia of the atlas: report of three cases and literature review.

作者信息

Nishikawa K, Ludwig S C, Colón R J, Fujimoto Y, Heller J G

机构信息

Hiroshima City Hospital, Hiroshima, Japan.

出版信息

Spine (Phila Pa 1976). 2001 Mar 1;26(5):E80-6. doi: 10.1097/00007632-200103010-00003.

Abstract

STUDY DESIGN

Case reports of patients with cervical myelopathy to hypoplasia of the atlas.

OBJECTIVES

To report cases of cervical myelopathy due to congenital hypoplasia of the atlas and to review the literature.

SUMMARY OF BACKGROUND DATA

Six previously documented cases of congenital hypoplasia of the atlas as a cause of cervical myelopathy are reported in the literature.

METHODS

Three patient's clinical record and radiologic imaging studies as well as a thorough literature search are reported. Plain radiographs, computed tomography scans, magnetic resonance images, as well as somatosensory-evoked potential changes are displayed.

RESULTS

Cervical myelopathy developed in three patients who were found to have congenital hypoplasia of the atlas. Laminectomy of C1 provided neurologic improvement in all three patients presented.

CONCLUSION

Congenital hypoplasia of the atlas is a rare cause of cervical myelopathy. This report should broaden the radiographic differential diagnosis when seeking an explanation for the signs and symptoms of cervical myelopathy.

摘要

研究设计

寰椎发育不全导致颈椎脊髓病患者的病例报告。

目的

报告因寰椎先天性发育不全导致颈椎脊髓病的病例并复习相关文献。

背景资料总结

文献报道了6例先前记录的因寰椎先天性发育不全导致颈椎脊髓病的病例。

方法

报告了3例患者的临床记录、放射影像学研究以及全面的文献检索情况。展示了X线平片、计算机断层扫描、磁共振成像以及体感诱发电位变化。

结果

3例被发现有寰椎先天性发育不全的患者出现了颈椎脊髓病。对所有3例患者进行C1椎板切除术均使神经功能得到改善。

结论

寰椎先天性发育不全是颈椎脊髓病的罕见病因。本报告应拓宽在寻求颈椎脊髓病症状和体征解释时的影像学鉴别诊断范围。

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