Lowes M, Bojsen-Møller M, Vorre P, Hedegaard O
Acta Neurochir (Wien). 1978;43(3-4):201-6. doi: 10.1007/BF01587956.
Thirteen cases of the childhood type of optic glioma from a 10-year period were studied. Particular attention was paid to the pre-operative neuro-ophthalmological and radiological findings. The patients all underwent explorative craniotomy when biopsy specimens were removed for histopathological study. Post-operative radiotherapy was given in 12 cases. In the follow-up period five patients showed deterioration of visual function, three patients showed unchanged visual function, and one patient showed improved visual function. In the remaining four patients, visual function could not be adequately determined. Three patients died in the course of the follow-up period. Retrospectively it was possible, on a histopathological basis, to divide the patients into three groups. It is suggested that the future management of these patients should consist of explorative craniotomy with diagnostic biopsy. Radiotherapy should be confined to selected cases, as only a minority of optic gliomas are radiosensitive.
对10年间13例儿童型视神经胶质瘤病例进行了研究。特别关注术前神经眼科和放射学检查结果。所有患者均接受了探查性开颅手术,术中获取活检标本进行组织病理学研究。12例患者术后接受了放疗。在随访期间,5例患者视力功能恶化,3例患者视力功能无变化,1例患者视力功能改善。其余4例患者的视力功能无法充分评估。3例患者在随访期间死亡。回顾性地,根据组织病理学结果,有可能将患者分为三组。建议对这些患者的未来治疗应包括进行诊断性活检的探查性开颅手术。放疗应限于选定的病例,因为只有少数视神经胶质瘤对放疗敏感。