Controversy in the management of optic pathway gliomas. 29 patients treated with radiation therapy at Baylor College of Medicine from 1967 through 1987.

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

Abstract

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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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。
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。
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Optic Pathway Gliomas Exposure of newborn mice to adenosine causes neural crest dysplasia and tumor formation. Summary of patient data from a multidisciplinary neurofibromatosis clinic. Hemimegalencephaly, hemifacial hypertrophy and intracranial lipoma: a variant of neurofibromatosis. Neurofibromatosis in Gothenburg, Sweden. II. Intellectual compromise.
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