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一名年轻患者最初表现为四肢瘫,其C5椎体发生侵袭性颈椎骨母细胞瘤:病例报告及文献复习

Destructive cervical spine osteoblastoma at C5 in a young patient initially presenting with quadriparesis: case report and review of the literature.

作者信息

Argyriou Andreas A, Panagiotopoulos Vasileios, Masmanidis Aristeidis, Tzortzidis Fotios, Konstantinou Dimitrios

机构信息

Department of Neurology, Saint Andrew's General Hospital of Patras, Patras, Greece.

出版信息

J Emerg Med. 2013 Jan;44(1):e1-4. doi: 10.1016/j.jemermed.2011.05.089. Epub 2011 Dec 22.

DOI:10.1016/j.jemermed.2011.05.089
PMID:22197196
Abstract

BACKGROUND

Osteoblastomas are rare benign bone tumors that are mostly found in the posterior spinal elements; about 20% are located in the cervical spine.

OBJECTIVE

The case of a destructive cervical osteoblastoma at C5 is reported in a 19-year-old man who initially presented with spastic quadriparesis.

CASE REPORT

A 19-year-old man was self-referred, reporting symptoms in keeping with a progressive spastic quadriparesis, which had suddenly developed 6 days earlier. Preceding symptoms included mild non-specific neck pain for 3 weeks. The patient was afebrile, and no ambulatory X-ray study had been performed until the time of referral. A cervical spine computed tomography (CT) scan revealed a lytic lesion involving the spinal process and the pedicles of the C5 vertebra. Cervical spine magnetic resonance imaging performed on an inpatient basis revealed a well-circumscribed, destructive lesion of the C5 vertebra, measuring approximately 3 cm. The spinal cord was significantly compressed. The patient underwent open surgical resection of the tumor through a midline posterior approach. Histopathology of the tumor specimen was in keeping with a diagnosis of osteoblastoma.

CONCLUSION

Neuroimaging should be performed with either conventional plain X-ray study, which seems to be sufficient in patients presenting with non-specific symptomatology related to cervical spine damage, or with advanced techniques in the case of patients with persistent neck pain or neurological deficit.

摘要

背景

骨母细胞瘤是一种罕见的良性骨肿瘤,大多位于脊柱后部结构;约20%位于颈椎。

目的

报告一例19岁男性C5椎体侵袭性颈椎骨母细胞瘤病例,该患者最初表现为痉挛性四肢瘫。

病例报告

一名19岁男性自行前来就诊,自述症状符合进行性痉挛性四肢瘫,此症状于6天前突然出现。之前的症状包括3周的轻度非特异性颈部疼痛。患者无发热,转诊时未进行门诊X线检查。颈椎计算机断层扫描(CT)显示C5椎体棘突和椎弓根有溶骨性病变。住院期间进行的颈椎磁共振成像显示C5椎体有一个边界清晰的侵袭性病变,大小约3厘米。脊髓明显受压。患者通过后正中入路接受了肿瘤开放手术切除。肿瘤标本的组织病理学检查结果符合骨母细胞瘤的诊断。

结论

对于出现与颈椎损伤相关的非特异性症状的患者,可采用传统的普通X线检查进行神经影像学检查,这似乎就足够了;对于持续颈部疼痛或神经功能缺损的患者,则应采用先进技术进行检查。

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