Wright J E, McDonald W I, Call N B
Br J Ophthalmol. 1980 Aug;64(8):545-52. doi: 10.1136/bjo.64.8.545.
Seventeen patients thought to have orbital optic nerve gliomas when first seen have been reviewed after up to 12 years. Enlargement of the optic canal was present in 15 of the 16 patients examined, but this finding was unreliable as an indicator of the posterior extent of the tumour. Nine patients had a stable course with little change over a period of up to 8 years; there was optic atrophy in all and neurofibromatosis was relatively common (7/9). Eight patients showed progressive enlargement of the tumour; 6 had swollen discs, and the incidence of neurofibromatosis was relatively low (3/8). The optic nerve was excised in 7 of the latter group. Biopsies of the optic nerve taken from the region of maximal enlargement were difficult to interpret and unhelpful in planning management. Radical surgery should be reserved for the minority of patients in whom there is progressively enlarging tumour without evidence of chiasmal involvement.
17例初诊时被认为患有眶内视神经胶质瘤的患者,经过长达12年的随访观察。在接受检查的16例患者中,有15例存在视神经管扩大,但这一发现作为肿瘤向后延伸范围的指标并不可靠。9例患者病情稳定,长达8年几乎没有变化;所有患者均出现视神经萎缩,神经纤维瘤病相对常见(7/9)。8例患者肿瘤呈进行性增大;6例视盘肿胀,神经纤维瘤病的发生率相对较低(3/8)。后一组中有7例切除了视神经。从肿瘤最大扩大区域获取的视神经活检标本难以解读,对治疗方案的制定也没有帮助。根治性手术应仅适用于少数肿瘤进行性增大且无视交叉受累证据的患者。