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Gliosarcoma arising from a fibrillary astrocytoma.

机译:由纤维状星形细胞瘤引起的神经胶质肉瘤。

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摘要

We report a 67-year-old woman who was diagnosed with a gliosarcoma at a second operation after diagnosis of a fibrillary astrocytoma 5 months previously. Initially, she underwent a CT-guided stereotactic biopsy. Histological examination showed fibrillary astrocytoma (World Health Organization [WHO] grade II). Loss of heterozygosity (LOH) on 1p, 10q, and 19q was not detected. She received chemotherapy, but no radiotherapy. Five months after the biopsy, MRI revealed rapid tumor growth. Tissue obtained from partial removal of the tumor revealed gliosarcoma (WHO grade IV), and LOH on 10q and 19q was detected. The history, histopathology, and genetic alterations of this patient are discussed.
机译:我们报告了一个67岁的妇女,她在5个月前被诊断出纤维状星形细胞瘤后,在第二次手术中被诊断出患有神经胶质肉瘤。最初,她接受了CT引导的立体定向活检。组织学检查显示纤维状星形细胞瘤(世界卫生组织[WHO] II级)。未检测到1p,10q和19q杂合度(LOH)的丢失。她接受了化疗,但未接受放疗。活检五个月后,MRI显示肿瘤快速生长。部分切除肿瘤获得的组织显示为神经胶质肉瘤(WHO IV级),并且在10q和19q处检测到LOH。讨论了该患者的病史,组织病理学和遗传改变。

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