Rush J A, Younge B R, Campbell R J, MacCarty C S
Ophthalmology. 1982 Nov;89(11):1213-9.
Eighty-five cases of histologically verified gliomas of the optic nerve or chiasm were studied retrospectively. Patient survival was analyzed according to location of tumor, treatment received, presence of neurofibromatosis, and degree of histologic anaplasia. Thirty-three patients had optic nerve tumors, and 52 had tumors involving the chiasm. Follow-up ranged from 6 days to 43.7 years. Of the 33 patients with optic nerve tumors, 28 (85%) survived a mean duration of 17 years, and survival was significantly associated with completeness of surgical excision. Twenty-three of the 52 patients (44%) with chiasmal tumors survived a mean duration of 19 years. Survival among patients with chiasmal tumors was unrelated to therapy received and was affected adversely by concomitant involvement of adjacent brain structures. The presence of neurofibromatosis conferred a protective benefit to patients with chiasmal tumors. No other significant factors could be statistically identified to influence the prognosis of patients with optic gliomas.
对85例经组织学证实的视神经或视交叉胶质瘤患者进行了回顾性研究。根据肿瘤位置、接受的治疗、神经纤维瘤病的存在情况以及组织学间变程度分析患者生存率。33例患者患有视神经肿瘤,52例患者患有累及视交叉的肿瘤。随访时间从6天到43.7年不等。在33例视神经肿瘤患者中,28例(85%)存活,平均存活时间为17年,生存率与手术切除的完整性显著相关。52例视交叉肿瘤患者中有23例(44%)存活,平均存活时间为19年。视交叉肿瘤患者的生存率与接受的治疗无关,且受相邻脑结构同时受累的不利影响。神经纤维瘤病的存在对视交叉肿瘤患者有保护作用。在统计学上未发现其他显著因素影响视神经胶质瘤患者的预后。