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Glioblastoma Multiforme in a Patient with Isolated Hemimegalencephaly

机译:多形性胶质母细胞瘤在孤立性半巨脑患者中的作用

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摘要

We present an exceptional case of a patient with hemimegalencephaly and secondary intractable epilepsy treated with vagus nerve stimulation (VNS) and subsequent glioblastoma development in the hemimegalencephalic hemisphere 6 years after surgery. VNS (at age 18 years) led to a 60% reduction of intractable seizures. However, symptoms of intracranial hypertension suddenly occurred 6 years after surgery. A computed tomography scan revealed a brain tumor in the hemimegalencephalic hemisphere. Pathologic examination confirmed glioblastoma multiforme. The genetic background of hemimegalencephaly is discussed here, with attention paid to the available data about the malignant transformation of malformations of cortical development (MCDs). The case points to the need for adequate clinical and radiologic follow-up care for patients with MCDs including hemimegalencephaly.
机译:我们介绍了一个例外情况,即术后6年,接受迷走神经刺激(VNS)治疗的半巨脑和继发性顽固性癫痫患者,随后在半巨脑半球发展成胶质母细胞瘤。 VNS(18岁)使顽固性癫痫发作减少了60%。然而,术后6年颅内高压症状突然发生。计算机断层扫描显示在半大脑半球有脑瘤。病理检查证实多形性胶质母细胞瘤。此处讨论了半巨脑的遗传背景,并注意有关皮质发育畸形(MCD)恶变的可用数据。该病例表明需要对包括半巨脑症在内的MCD患者进行充分的临床和放射学随访护理。

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