视神经胶质瘤治疗的争议。从1967年到1987年贝勒医学院有29名患者接受了放射治疗。

Neurofibromatosis Pub Date : 1988-01-01
J D Easley, L Scharf, J L Chou, V M Riccardi
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引用次数: 0

摘要

本文对29例视神经胶质瘤患者进行x线治疗,其中14例为von Recklinghausen神经纤维瘤病(NF-1)。数据显示,所有29例患者的20年预计生存率为92%。此外,在NF-1患者中,86%稳定或改善,而在非NF-1患者中,只有47%稳定或改善。因此,这些数据表明,NF-1患者的视神经胶质瘤的生物生理行为存在差异,同时,通过改善或稳定视力来衡量放射治疗的有益反应,无论有无伴随肿瘤消退的放射学证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controversy in the management of optic pathway gliomas. 29 patients treated with radiation therapy at Baylor College of Medicine from 1967 through 1987.

The optic gliomas of 29 patients, including 14 with von Recklinghausen neurofibromatosis (NF-1), were subjected to X-ray therapy. The data indicate a projected 20-year survival rate of 92% for all 29 patients. Moreover, among the NF-1 patients, 86% were stabilized or improved, while among non-NF-1 patients, only 47% stabilized or were improved. Thus, these data suggest that there are differences in the biophysiological behavior of optic nerve gliomas in patients with NF-1, and, as well, that there is a salutary response to radiation treatment as measured by improvement or stabilization of vision, with and without radiologic evidence of concomitant tumor regression.

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