首页> 美国卫生研究院文献>The British Journal of Ophthalmology >Childhood chiasmal gliomas: update on the fate of patients in the 1969 San Francisco Study.
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Childhood chiasmal gliomas: update on the fate of patients in the 1969 San Francisco Study.

机译:儿童期神经胶质瘤:1969年旧金山研究中患者命运的最新情况。

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摘要

We review the current status of 28 patients with chiasmal glioma who were originally reported on by Hoyt and Baghdassarian in 1969. The median period of follow-up was 20 years. Sixteen patients are now dead, five from chiasmal glioma and the rest from other causes. Four of the five deaths from chiasmal glioma occurred before 1969. The mortality rate in patients with neurofibromatosis and those without neurofibromatosis was essentially the same. Nine of 16 patients with neurofibromatosis are dead, two from chiasmal glioma, one from aspiration, and six from another tumour. Seven of 12 patients without neurofibromatosis are dead, three from chiasmal glioma, two from an operation on their tumour, and two from a medical illness. In general the quality of life of the surviving patients is good; none reported having a noticeable decrease in vision since 1969.
机译:我们回顾了Hoyt和Baghdassarian最初于1969年报道的28例伴有神经胶质瘤的患者的现状。随访的中位时间为20年。现在有16例患者死亡,其中5例是由于胫骨神经胶质瘤死亡,其余的是由于其他原因。导致的5例死亡中,有4例发生在1969年之前。神经纤维瘤病患者和无神经纤维瘤病患者的死亡率基本相同。在16例神经纤维瘤病患者中有9例死亡,其中2例来自裂殖性神经胶质瘤,1例由于误吸,6例由于另一种肿瘤死亡。 12例无神经纤维瘤病的患者中有7例死亡,其中3例是由于颊神经胶质瘤死亡,2例是由于肿瘤手术,另外2例是由于医疗疾病。一般来说,幸存患者的生活质量良好;自1969年以来,没有人报告视力明显下降。

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