论文部分内容阅读
神经节胶质瘤是颅内少见肿瘤,我们手术证实1例,报告如下。 病例摘要 患者 男,31岁,癫痫11年,药物控制无效,于1989年5月11日入神经内科。患者自1978年3月无明显诱因出现癫痫大发作。以后每月发作一次,多在夜间发病。在外院服抗痫灵治疗,效果不佳。入我院后,经CT扫描,发现右颞对低密度灶,增强后无明显强化,无占位效应,报告为软化灶。患者无外伤史、无中耳炎及乳突炎病史和家族史。
Ganglionoma glioma is a rare intracranial tumor. We confirmed one case by surgery. The report is as follows. Case summary Patient Male, 31 years old, 11 years of epilepsy, drug control was ineffective, and entered the Department of Neurology on May 11, 1989. The patient had no major cause of seizures since March 1978. After the onset of monthly episodes, more often at night. In hospitals serving anti-eclampsia treatment, the effect is not good. After being admitted to our hospital, after CT scan, it was found that the right eyelid had low density lesions, no enhancement after enhancement, no mass effect, and soften lesions were reported. The patient had no history of trauma, no history of otitis media, and mastoiditis and family history.