Chou Erh-Kang, Chang Chun-Shin, Chen Philip Kuo-Ting, Chen Yu-Ray, Yu Jack Chung-Kai, Jung Shih-Ming, Chang Sophia Chia-Ning
Department of Plastic Surgery, School of Medicine, China Medical University Hospital, China Medical University, Taichung, Taiwan.
J Craniofac Surg. 2009 Mar;20(2):406-9. doi: 10.1097/SCS.0b013e31819b9641.
Primary osteosarcoma of the calvarium is rare. A 22-year-old female patient was admitted for a progressively enlarging, indurated mass under her scalp for 6 months. A computed tomographic scan revealed a 4 x 3 x 2-cm3 osteolytic lesion over the right parietal cortex with a sunburst appearance. The patient underwent en bloc tumor resection using bicortical parietal craniectomy with a 2-cm margin of normal bone, including the tightly adherent periosteum over the tumor. Immediate cranioplasty was performed with split-thickness autogenous calvarial bone grafts. Histopathologic examination showed the tumor to be a primary high-grade osteosarcoma of the skull. She received postoperative chemotherapy. She has recovered well and remains without any evidence of disease at her most recent, 8-year follow-up. The key to disease-free survival in treating primary osteosarcoma of the calvarium is complete surgical resection with immediate reconstruction followed by adjuvant chemotherapy.
颅骨原发性骨肉瘤较为罕见。一名22岁女性患者因头皮下肿物进行性增大、变硬6个月入院。计算机断层扫描显示右侧顶叶皮质有一个4×3×2立方厘米的溶骨性病变,呈日光放射状外观。患者接受了整块肿瘤切除术,采用双皮质顶骨颅骨切除术,切缘为正常骨2厘米,包括肿瘤上紧密粘连的骨膜。立即用自体颅骨劈开骨移植进行颅骨成形术。组织病理学检查显示肿瘤为颅骨原发性高级别骨肉瘤。她接受了术后化疗。她恢复良好,在最近8年的随访中未发现任何疾病迹象。治疗颅骨原发性骨肉瘤实现无病生存的关键是完整的手术切除并立即重建,随后进行辅助化疗。