神经鞘瘤
神经纤维瘤病
医学
星形细胞瘤
胶质瘤
2型神经纤维瘤病
自然史
病变
神经纤维瘤
纤维神经瘤
病理
神经纤维蛋白1
脑膜瘤
内科学
癌症研究
作者
Chuiguang Kong,Xiaosheng He
出处
期刊:Chinese Journal of Neuromedicine
日期:2019-07-15
卷期号:18 (7): 732-735
标识
DOI:10.3760/cma.j.issn.1671-8925.2019.07.016
摘要
Patients with type II neurofibromatosis often have multiple neurological tumors, including schwannoma, meningioma, astrocytoma and ependymoma, of which bilateral vestibular schwannoma is characteristic lesion. More than 90% of familial cases and 80%-85% of sporadic cases of type II neurofibromatosis have been confirmed to have neurofibromatosis II gene mutations in both tumor tissues and blood. This article reviews the relation of type II neurofibromatosis with different types of tumors, and the incidence, natural history and latest treatment strategies of type II neurofibromatosis, in order to provide new clues for diagnoses and treatments of patients with type II neurofibromatosis complicated with multi-type tumors.
Key words:
Neurofibromatosis II; Neurilemmoma; Meningioma; Glioma
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