Doskaliyev Aidos, Yamasaki Fumiyuki, Kenjo Masahiro, Shrestha Prabin, Saito Taiichi, Hanaya Ryosuke, Sugiyama Kazuhiko, Kurisu Kaoru
Department of Neurosurgery, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
J Neurooncol. 2008 Jul;88(3):299-303. doi: 10.1007/s11060-008-9564-y. Epub 2008 Mar 29.
Secondary brain tumors rarely arise after cranial irradiation; among them, meningiomas and glioblastomas are the most common and secondary oligodendroglial tumors the most rare. We present a 48-year-old man who developed an oligodendroglial tumor 38 years after receiving 50 Gy of cranial irradiation to a pineal tumor. He underwent gross total removal of a calcified, ring-enhanced mass in the right temporal lobe. The tumor was histologically diagnosed as anaplastic oligodendroglioma. Our review of previously reported secondary oligodendroglial tumors that developed after cranial irradiation revealed that these rare tumors arose after low-dose cranial irradiation or at the margin of a field irradiated with a high dose. We suggest that secondary oligodendroglial tumors arising after cranial irradiation are more aggressive than primary oligodendrogliomas.
继发性脑肿瘤很少在颅脑放疗后发生;其中,脑膜瘤和胶质母细胞瘤最为常见,而继发性少突胶质细胞瘤最为罕见。我们报告一名48岁男性,他在因松果体肿瘤接受50 Gy颅脑放疗38年后发生了少突胶质细胞瘤。他接受了右侧颞叶钙化、环形强化肿块的全切除。肿瘤经组织学诊断为间变性少突胶质细胞瘤。我们对先前报道的颅脑放疗后发生的继发性少突胶质细胞瘤进行回顾发现,这些罕见肿瘤发生于低剂量颅脑放疗后或高剂量照射野的边缘。我们认为,颅脑放疗后发生的继发性少突胶质细胞瘤比原发性少突胶质细胞瘤更具侵袭性。