Noshita Nobuo, Mashiyama Shoji, Fukawa Osamu, Asano Shigeyuki, Watanabe Mika, Tominaga Teiji
Department of Neurosurgery, Iwaki Kyoritsu General Hospital, Iwaki, Fukushima.
Neurol Med Chir (Tokyo). 2010;50(2):161-4. doi: 10.2176/nmc.50.161.
We report a rare case of anaplastic oligodendroglioma with extracranial metastasis, showing 1p19q co-deletion in both the brain tissue and the metastatic site. A 53-year-old man first presented with a left frontal tumor. The tumor was subtotally removed and irradiation was performed for the residual tumor and tumor bed. Two years after the initial treatment, several tumors appeared on his neck and one was resected. Histological examination revealed anaplastic oligodendroglioma, proved to be the same as the previous brain tumor. The patient refused further treatment, and died 30 months after the initial treatment. Autopsy demonstrated multiple extracranial metastases in the vertebrae, lymph nodes, spinal dura mater, thymus gland, and chest wall. We confirmed 1p19q loss of heterozygosity in both lesions, suggesting that 1p19q co-deletion might important to extracranial metastasis of oligodendroglioma.
我们报告了一例罕见的间变性少突胶质细胞瘤伴颅外转移病例,该病例在脑组织和转移部位均显示1p19q共缺失。一名53岁男性最初表现为左额叶肿瘤。肿瘤次全切除,并对残留肿瘤和肿瘤床进行了放疗。初始治疗两年后,他的颈部出现了几个肿瘤,其中一个被切除。组织学检查显示为间变性少突胶质细胞瘤,证实与先前的脑肿瘤相同。患者拒绝进一步治疗,在初始治疗30个月后死亡。尸检显示在椎骨、淋巴结、硬脊膜、胸腺和胸壁有多处颅外转移。我们在两个病灶中均证实了1p19q杂合性缺失,提示1p19q共缺失可能对少突胶质细胞瘤的颅外转移具有重要意义。