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Solitary thoracic osteochondroma causing spinal compression: Case report

机译:孤独的胸骨骨质粒细胞造成脊柱压缩:案例报告

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摘要

Spinal osteochondromas are very rare, and they present with nonspecific localized pain owing to bone involvement. Diagnosis is made based on direct X-ray and computed tomography (CT) imaging of the exophytic bone lesion with pedunculated or sessile structure. Although asymptomatic patients can be observed, surgical excision is the main treatment modality. We present the case of a 34-year-old man with solitary thoracic osteochondroma. The patient presented with complaints of pain in the legs, numbness, and inability to walk. The diagnosis was confirmed with CT imaging showing calcified heterogeneous bone lesion originating from the left side of T1-2 facet joint. After total excision, histopathological examination revealed the diagnosis of osteochondroma. No new clinical or radiological findings were detected in the 10-month follow-up.
机译:脊髓骨孔粒细胞非常罕见,它们由于骨累累而存在非特异性局部疼痛。诊断是基于与脱脂骨病变的直接X射线和计算断层扫描(CT)成像与致命的或无梗塞结构进行。虽然可以观察到无症状患者,但外科切除是主要的治疗方式。我们展示了一个34岁男性的孤零性胸骨骨质骨瘤的案例。患者患有腿部疼痛的抱怨,麻木,无法走路。用CT成像证实了诊断,显示源自T1-2小关节左侧的钙化异质骨病变。完全切除后,组织病理学检查揭示了骨质粒细胞瘤的诊断。在10个月的随访中没有检测到新的临床或放射性发现。

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