Oliveira Carolina, Vital Luísa, Serdoura Francisco, Pinho André Rodrigues, Veludo Vitorino
Departamento de Cirurgia Ortopédica, Unidade Local de Saúde do Alto Minho, Viana do Castelo, Portugal.
Departamento de Cirurgia Ortopédica, Hospital de São João, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
Rev Bras Ortop (Sao Paulo). 2019 Apr;54(2):219-222. doi: 10.1016/j.rboe.2017.11.017. Epub 2019 May 10.
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.
骨母细胞瘤是一种罕见的原发性良性骨肿瘤。它占良性骨肿瘤的3%，占所有原发性骨肿瘤的1%。治疗目标是完整的手术切除。这种治疗方法可降低复发风险。由于骨母细胞瘤是一种血管丰富的肿瘤，完整切除往往很困难。本报告描述了一名19岁男性患者的病例，该患者出现严重的右侧颈部和肩部疼痛。计算机断层扫描显示C7处有一个与骨母细胞瘤相符的肿块病变。进行了术前栓塞和肿瘤切除。在3年的随访中，患者的日常活动没有受限，迄今为止，没有复发的迹象。
