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一例形态学不典型的寰枢椎旋转半脱位。

A morphologically atypical case of atlantoaxial rotatory subluxation.

作者信息

Umebayashi Daisuke, Hara Masahito, Nishimura Yusuke, Wakabayashi Toshihiko

机构信息

Department of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.

出版信息

J Korean Neurosurg Soc. 2014 May;55(5):284-8. doi: 10.3340/jkns.2014.55.5.284. Epub 2014 May 31.

Abstract

A rare case of atlantoaxial rotatory subluxation occurred after pediatric cervical spine surgery performed to remove a dumbbell-shaped meningioma at the level of the C1/C2 vertebrae. This case is classified as a post-surgical atlantoaxial rotatory subluxation, but has a very rare morphology that has not previously been reported. Although there are several reports about post-surgical atlantoaxial rotatory subluxation, an important point of this case is that it might be directly related to the spinal cord surgery in C1/C2 level. On day 6 after surgery, the patient presented with the Cock Robin position, and a computed tomography scan revealed a normal type of atlantoaxial rotatory subluxation. Manual reduction was performed followed by external fixation with a neck collar. About 7 months after the first surgery, the subluxation became severe, irreducible, and assumed an atypical form where the anterior tubercle of C1 migrated to a cranial position, and the posterior tubercle of C1 and the occipital bone leaned in a caudal direction. The pathogenic process suggested deformity of the occipital condyle and bilateral C2 superior facets with atlantooccipital subluxation. A second operation for reduction and fixation was performed, and the subluxation was stabilized by posterior fixation. We encountered an unusual case of a refractory subluxation that was associated with an atypical deformity of the upper spine. The case was successfully managed by posterior fixation.

摘要

1例罕见的寰枢椎旋转半脱位发生在小儿颈椎手术后,该手术旨在切除C1/C2椎体水平的哑铃形脑膜瘤。此病例被归类为术后寰枢椎旋转半脱位,但具有一种非常罕见的形态,此前未见报道。虽然有几篇关于术后寰枢椎旋转半脱位的报道,但该病例的一个重要点是它可能与C1/C2水平的脊髓手术直接相关。术后第6天,患者出现“知更鸟”姿势,计算机断层扫描显示为正常类型的寰枢椎旋转半脱位。进行了手法复位,随后用颈托进行外固定。首次手术后约7个月,半脱位变得严重、不可复位,并呈现出一种非典型形式,即C1前结节向头侧移位,C1后结节和枕骨向尾侧倾斜。致病过程提示枕髁和双侧C2上关节面畸形伴寰枕半脱位。进行了第二次复位和固定手术,通过后路固定使半脱位得到稳定。我们遇到了1例与上颈椎非典型畸形相关的难治性半脱位的罕见病例。该病例通过后路固定成功治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/759c/4130956/fe001a58f97c/jkns-55-284-g001.jpg

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