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首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Lipidized glioblastoma: Pathological and molecular characteristics
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Lipidized glioblastoma: Pathological and molecular characteristics

机译:脂化胶质母细胞瘤:病理和分子特征

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摘要

We report a rare case of a 33-year-old man with a lipidized glioblastoma multiforme (GBM) in the right posterior frontal region. Histologically the tumor had all the typical features of a GBM but with the rare observation of lipidized differentiation. There were multiple mitoses, extensive vascular proliferation, focal necrosis and the tumor cells had abundant xanthomatous cytoplasm and marked nuclear pleomorphism. The tumor showed immunoreactivity with GFAP. The O6- methylguanine methyltransferase (MGMT) promoter was methylated and there were no isocitrate dehydrogenase (IDH)1 and IDH2 mutations. To the best of our knowledge, this is the first time MGMT promoter status and IDH mutation assessment have been reported in a case of lipidized GBM.
机译:我们报告了一个罕见的病例,该患者中右后额叶区域患有脂化性胶质母细胞瘤(GBM),现年33岁。从组织学上讲,肿瘤具有GBM的所有典型特征,但很少见脂化分化。有多个有丝分裂,广泛的血管增生,局灶性坏死,肿瘤细胞具有丰富的黄瘤细胞质,并具有明显的核多态性。肿瘤显示出与GFAP的免疫反应性。 O6-甲基鸟嘌呤甲基转移酶(MGMT)启动子被甲基化,并且没有异柠檬酸脱氢酶(IDH)1和IDH2突变。据我们所知,这是脂类GBM首次报道MGMT启动子状态和IDH突变评估。

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