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单侧前庭神经鞘瘤和其他神经源性肿瘤患者会有哪些影响?

What are the implications in individuals with unilateral vestibular schwannoma and other neurogenic tumors?

作者信息

Evans D Gareth R, Ramsden Richard T, Shenton Andrew, Gokhale Carolyn, Bowers Naomi, Huson Susan M, Wallace Andrew J

机构信息

Academic Unit of Medical Genetics, Regional Genetics Service and National Genetics Reference Laboratory, St. Mary's Hospital, Manchester, United Kingdom.

出版信息

J Neurosurg. 2008 Jan;108(1):92-6. doi: 10.3171/JNS/2008/108/01/0092.

Abstract

OBJECTIVES

Individuals who develop a unilateral vestibular schwannoma (VS) and other neurogenic tumors are at high risk of having the inherited condition neurofibromatosis Type 2 (NF2). The risk of bilateral disease and transmission risk to offspring are important in surgical planning and counseling. The authors have attempted to resolve these risks.

METHODS

A large NF2 dataset was interrogated for individuals who had initially presented with a unilateral VS and other tumors before developing bilateral disease, to assess the contralateral and offspring risks.

RESULTS

Ninety-six patients with a unilateral VS and additional neurogenic tumors had a bilaterality rate of 48% at 20 years in those initially diagnosed when > 18 years of age and 82% if presenting earlier. Constitutional NF2 mutations were found in blood in 25 (27%) of 92, but 13 (76%) of 17 patients presenting with unilateral VS at < or = 18 years of age. Tumor analysis suggests that the vast majority of the remainder are mosaic for an NF2 mutation.

CONCLUSIONS

Patients with unilateral VS and other NF2-related tumors who fulfill Manchester criteria have a high risk of developing a contralateral tumor, especially if presenting in childhood. Transmission risks are reduced for offspring, particularly in the older patients who are likely to be mosaic.

摘要

目的

罹患单侧前庭神经鞘瘤(VS)及其他神经源性肿瘤的个体患遗传性2型神经纤维瘤病(NF2)的风险很高。双侧患病风险及遗传给后代的风险在手术规划和咨询中很重要。作者试图解决这些风险问题。

方法

对一个大型NF2数据集进行调查,以了解那些在出现双侧疾病之前最初表现为单侧VS和其他肿瘤的个体,从而评估对侧及后代的患病风险。

结果

96例患有单侧VS及其他神经源性肿瘤的患者,若最初诊断时年龄大于18岁,20年时双侧患病发生率为48%;若发病较早,发生率为82%。92例患者中有25例(27%)血液中检测到遗传性NF2突变,但17例18岁及以下出现单侧VS的患者中有13例(76%)检测到该突变。肿瘤分析表明,其余绝大多数患者为NF2突变的嵌合体。

结论

符合曼彻斯特标准的单侧VS及其他NF2相关肿瘤患者发生对侧肿瘤的风险很高,尤其是在儿童期发病者。后代的遗传风险降低,特别是在可能为嵌合体的老年患者中。

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