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我院收治了一组二代人中三人患颅内肿瘤、现报告如下: 例1 冯××,男 14岁 因间断性癫痫大发作9年于1972年7月5日入空军西安医院。查体:神经系统无异常。经左颈总动脉造影示左额颞叶占位性病变。手术切除左额颞肿瘤,大小约3×3×3cm,病理报告为星形细胞瘤Ⅰ级。术后第7年开始出现癫痫发作,每年10余次,经用抗癫痫药治疗,症状控制。现术后15年CT检查未发现肿瘤复发,目前已参加工作。 例2 冯×× 男 25岁 例1胞兄。因右下肢无力伴视物模糊4个月于1974年6月24日入院。查体:神志清楚,左眼球稍突出,左眼颞测偏盲,颈有抵抗,双眼底视乳头水肿,
Our hospital admitted to a group of two generations of three people suffering from intracranial tumors, are as follows: Example 1 Feng × ×, male 14 years old due to intermittent epilepsy episode 9 years in July 5, 1972 Air Force Xi’an Hospital. Physical examination: no abnormal nervous system. Left carotid artery angiography showed the left frontal temporal lobe occupying lesions. Surgical removal of the left frontotemporal tumor, the size of about 3 × 3 × 3cm, the pathological report of astrocytoma grade Ⅰ. Seven years after the onset of seizures, more than 10 times per year, the use of antiepileptic drugs, symptoms control. Now 15 years CT examination found no recurrence of the tumor, has now joined the work. Example 2 Feng XX male 25-year-old case 1 brother. Due to the right lower extremity weakness with blurred vision 4 months on June 24, 1974 admission. Physical examination: conscious, slightly prominent left eye, left eye temporal hemianopia, neck resistance, binocular end of the nipple edema,