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放疗后治疗额部脑胶质瘤继发骨肉瘤 2 例报告

Radiation-induced osteosarcomas after treatment for frontal gliomas: a report of two cases.

机构信息

Department of Neurosurgery, Nakamura Memorial Hospital, Minami 1, Nishi 14, Sapporo, 060-8570, Japan.

出版信息

Brain Tumor Pathol. 2010 Oct;27(2):103-9. doi: 10.1007/s10014-010-0267-7. Epub 2010 Nov 3.

Abstract

Most radiation-induced osteosarcomas of the skull are reported to arise in the facial bone or paranasal sinus after radiotherapy for retinoblastoma and/or pituitary adenoma. Here we report two cases of radiation-induced osteosarcoma in the paranasal sinus after treatment for frontal glioma. Case 1 was a 56-year-old woman who underwent surgical resection of a left frontal tumor in October 1990. The histological diagnosis was a low-grade glioma, and radiotherapy of 54 Gy was administered. Sixteen years later, in September 2006, the patient noted an enlarging subcutaneous mass in the right frontal region. CT showed an osteolytic mass in the right frontal sinus. An open biopsy established the histopathological diagnosis of osteosarcoma, and the patient subsequently died of rapid tumor regrowth. Case 2 was a 58-year-old man who underwent partial removal of a bifrontal tumor in May 1996. The histological diagnosis was anaplastic oligoastrocytoma, and radiotherapy of 56 Gy was administered. Twelve years later, in March 2008, the patient was readmitted to our hospital for reasons of marked deterioration in general physical condition. Tumor recurrence was suspected in the left frontal lobe, and CT demonstrated an osteolytic mass in the left frontal and ethmoid sinus. A secondary operation was performed, and the pathological specimens were diagnosed as osteosarcoma. Radiotherapy was readministered, but the subject died of rapid tumor regrowth. From these clinicopathological findings, both cases were diagnosed as radiation-induced osteosarcoma. Radiation-induced osteosarcomas appeared 16 and 12 years after radiotherapy in cases 1 and 2, respectively. As the prognosis of radiation-induced osteosarcoma is poorer than that of primary osteo-sarcoma, careful attention is required for consideration of the long-term survival of patients with glioma.

摘要

大多数颅部放射诱导性骨肉瘤据报道是在接受视网膜母细胞瘤和/或垂体腺瘤放射治疗后发生于面骨或副鼻窦。在此,我们报告两例接受额部胶质瘤治疗后发生于副鼻窦的放射诱导性骨肉瘤。病例 1 为 56 岁女性,于 1990 年 10 月接受左侧额部肿瘤切除术。组织学诊断为低度恶性胶质瘤,并接受了 54 Gy 的放射治疗。16 年后,即 2006 年 9 月,患者注意到右侧额部有一个增大的皮下肿块。CT 显示右侧额窦溶骨性肿块。开放性活组织检查确立了骨肉瘤的组织病理学诊断,随后患者因肿瘤迅速复发而死亡。病例 2 为 58 岁男性,于 1996 年 5 月接受双额部部分切除术。组织学诊断为间变性少突星形细胞瘤,并接受了 56 Gy 的放射治疗。12 年后,即 2008 年 3 月,患者因一般健康状况明显恶化而再次入院。怀疑左侧额叶肿瘤复发,CT 显示左侧额窦和筛窦溶骨性肿块。进行了二次手术,病理标本诊断为骨肉瘤。给予放射治疗,但患者因肿瘤迅速复发而死亡。根据这些临床病理发现,两例均诊断为放射诱导性骨肉瘤。病例 1 和 2 分别在放射治疗后 16 年和 12 年出现放射诱导性骨肉瘤。由于放射诱导性骨肉瘤的预后比原发性骨肉瘤差,因此需要仔细关注胶质瘤患者的长期生存问题。

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