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Cervical Osteoblastoma: A Case Report

机译:宫颈成骨细胞瘤:一例报告

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摘要

Osteoblastoma is a rare benign primary bone tumor. It accounts for 3% of benign and 1% of all primary bone tumors. The treatment goal is complete surgical resection. This treatment limits the risk of recurrence. As osteoblastoma is a highly vascular tumor, complete resection is often difficult. This report describes the case of a 19-year-old male patient who presented severe right-sided neck and shoulder pain. The computed tomography scan revealed a mass lesion on C7 compatible with osteoblastoma. Preoperative embolization and tumor resection were performed. At the 3-year follow-up, the patient had no restrictions on daily activities, and, to date, there has been no evidence of recurrence.
机译:成骨细胞瘤是一种罕见的良性原发性骨肿瘤。它占所有原发性骨肿瘤的3%和1%。治疗目标是完成手术切除。这种治疗限制了复发的风险。由于成骨细胞瘤是高度血管性的肿瘤,因此通常难以完全切除。该报告描述了一名19岁的男性患者,该患者表现出严重的右侧颈部和肩部疼痛。计算机断层扫描显示与成骨细胞瘤相容的C7肿块。进行术前栓塞和肿瘤切除。在3年的随访中,患者对日常活动没有任何限制,并且迄今为止,还没有复发的迹象。

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