Mizoi K, Sato T, Kaneko U, Suzuki J
No Shinkei Geka. 1979 Sep;7(9):905-9.
A 3 1/2-year-old girl with a huge optic glioma was reported. On February 26, 1978, she was hospitalized for signs of increased intracranial pressure, namely headache, vomiting and consciousness disturbance. Before admission she did not complain of her visual disturbance. A huge mass lesion in the subfrontal-suprasellar region was found by neuroradiological examination. The operation was performed on March 7, 1978, and the tumor arising from the right optic nerve, about 170 grams in weight, was totally removed in piecemeals. Histopathological diagnosis was pilocytic astrocytoma. Immediately after operation diabetes insipidus and hypernatremia developed, but two months later these symptoms disappeared. Post-operative CT scan demonstrated no mass lesion in the subfrontal-suprasellar region. After radiation therapy, she was discharged with slight left hemiparesis on August 31, 1978. Though her right eye was blind, visual acuity remained 0.2 in the left eye. No other neurologic deficits could be found.
报告了一名3岁半患有巨大视神经胶质瘤的女孩。1978年2月26日,她因颅内压升高的症状,即头痛、呕吐和意识障碍而住院。入院前她未诉说视力障碍。经神经放射学检查发现额下-鞍上区域有一个巨大的肿块病变。于1978年3月7日进行了手术,从右侧视神经长出的肿瘤,重约170克,被分块全部切除。组织病理学诊断为毛细胞型星形细胞瘤。术后立即出现尿崩症和高钠血症,但两个月后这些症状消失。术后CT扫描显示额下-鞍上区域无肿块病变。放疗后,她于1978年8月31日带着轻度左侧偏瘫出院。虽然她的右眼失明,但左眼视力仍为0.2。未发现其他神经功能缺损。