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颈椎先天性后凸伴寰枢椎脱位。病例报告。

Cervical congenital kyphosis with atlantoaxial dislocation. A case report.

作者信息

Shiba R, Murota K, Kondo H, Honma G

机构信息

Department of Orthopaedic Surgery, Jikei University School of Medicine, Tokyo, Japan.

出版信息

Spine (Phila Pa 1976). 1993 May;18(6):762-3. doi: 10.1097/00007632-199305000-00015.

DOI:10.1097/00007632-199305000-00015
PMID:8516708
Abstract

Congenital kyphosis and atlantoaxial dislocation in a 13-year-old boy was treated by a C1 laminectomy and C2-C5 laminoplasty with fusion from the occiput to C2. This resulted in postoperative neurologic deterioration, but a secondary anterior C3 vertebrectomy followed by a C2-C5 fusion helped restore neural function. In the presence of congenital cervical kyphosis, anterior rather than posterior decompression and fusion is recommended, particularly in the presence of a stenotic spinal canal.

摘要

一名13岁男孩的先天性脊柱后凸和寰枢椎脱位采用C1椎板切除术和C2 - C5椎板成形术并进行枕骨至C2融合治疗。这导致术后神经功能恶化,但随后进行的二次C3椎体前路切除术及C2 - C5融合术有助于恢复神经功能。对于先天性颈椎后凸,建议采用前路而非后路减压和融合术,尤其是在存在椎管狭窄的情况下。

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引用本文的文献

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Commentary on "Weak Ligaments and Sloping Joints: A New Hypothesis for Development of Congenital Atlantoaxial Dislocation and Basilar Invagination".《弱韧带与倾斜关节:先天性寰枢椎脱位和基底凹陷症发展的新假说》述评
Neurospine. 2020 Dec;17(4):857-858. doi: 10.14245/ns.2040632.316. Epub 2020 Dec 31.
2
Apoptosis of endplate chondrocytes in post-laminectomy cervical kyphotic deformity. An in vivo animal model in sheep.椎板切除术后颈椎后凸畸形中端板软骨细胞的凋亡。绵羊体内动物模型。
Eur Spine J. 2013 Jul;22(7):1576-82. doi: 10.1007/s00586-013-2811-8. Epub 2013 May 5.