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Neoadjuvant temozolomide followed by complete resection of a 1p- and 19q-deleted anaplastic oligoastrocytoma: Case study1

机译:新辅助替莫唑胺,然后完全切除1p和19q缺失的间变性少星形胶质细胞瘤:案例研究1

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摘要

A 38-year-old woman presented with an infiltrative tumor of the right frontal lobe and genu of the corpus callosum that was deemed only partially resectable. A stereotactic biopsy was performed, which revealed a right frontal oligoastrocytoma that had some anaplastic features as well as allelic loss of chromosome arms 1p and 19q. The patient was treated with temozolomide for 24 months. The partial response of the tumor to chemotherapy rendered the lesion amenable to gross total resection, which was performed subsequently. The patient remains alive and well without evidence of recurrence 7 months after resection and 48 months after initial diagnosis. Thus, preoperative chemotherapy decreased tumor mass to a degree that subsequently enabled a gross total resection. This treatment strategy, although common in the treatment of other solid tumors, is rarely utilized in adult neuro-oncology and raises another potential role for chromosome testing in oligodendroglial tumor management.
机译:一名38岁妇女的右额叶浸润性肿瘤和call体属被认为只能部分切除。进行了立体定向活检,发现右额叶星形胶质细胞瘤具有一些变性的特征,以及染色体臂1p和19q的等位基因缺失。该患者接受替莫唑胺治疗24个月。肿瘤对化学疗法的部分反应使病变易于进行全切除,随后进行了切除。切除后7个月和初次诊断后48个月,患者仍然存活且无复发迹象。因此,术前化学疗法将肿瘤块减少到一定程度,随后可以进行总的切除。尽管这种治疗策略在其他实体瘤的治疗中很常见,但在成人神经肿瘤学中很少使用,并在少突神经胶质肿瘤管理中提高了染色体检测的另一潜在作用。

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