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Malignant transformation of an osteoblastoma of the mandible: case report and review of the literature

机译:下颌骨成骨细胞瘤的恶性转化:病例报告及文献复习

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Benign osteoblastoma is a rarely seen tumor of the facial bones. The authors present a case of a 30-year-old man with a tumor of the mandibular body and ramus. The histopathological diagnosis was one of osteoblastoma. Postoperative recurrence with soft tissue infiltration suggested an osteosarcoma radiologically, but the histological examination again revealed the presence of an osteoblastoma. A second recurrence occured in the pharyngo-glossal region and this time the tumor was histologically diagnosed as an osteoblastoma, but with foci of well-differentiated osteosarcoma. The patient was given a course of radiotherapy, but clinical and radiological examination 8 months later revealed lung metastases and chemotherapy was started. Unfortunately, the patient died months later. While osteoblastomas are rare, and their sarcomatous change even rarer, our experience with this case lead us to suggest that a therapeutic preventative approach, involving both chemotherapy and total excision of the tumor, is the regime to adopt with osteoblastomas which involve soft tissues and have radiological features suggesting malignancy.
机译:良性成骨细胞瘤是很少见的面骨肿瘤。作者介绍了一个30岁男子的下颌体和支具瘤的病例。组织病理学诊断是成骨细胞瘤之一。术后软组织浸润复发提示影像学上为骨肉瘤,但组织学检查再次显示存在成骨细胞瘤。第二次复发发生在咽-舌区,这次在组织学上被诊断为成骨细胞瘤,但有高度分化的骨肉瘤灶。对该患者进行了放疗,但8个月后临床和放射学检查发现有肺转移并开始了化疗。不幸的是,病人几个月后死亡。尽管成骨细胞瘤很少见,并且肉瘤的变化甚至更罕见,但我们的经验表明,这种治疗方法涉及化学疗法和肿瘤全切除术,是涉及软组织且具有以下特征的成骨细胞瘤的治疗方案:影像学特征提示恶性。

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