Benson Rony, Mallick Supriya, Julka Pramod K, Rath Goura K
Department of Radiation Oncology, All India Institute of Medical Sciences, New Delhi, India.
Neurol India. 2016 Mar-Apr;64(2):279-86. doi: 10.4103/0028-3886.177630.
An ependymoma is an uncommon glial tumor, which arises from different parts of the neuroaxis. Considerable variation in presentation and survival in tumors in different locations after an optimum treatment indicates inherent molecular and genetic differences in tumorigenesis between them. A number of genetic aberrations have been identified to distinctly characterize different subgroups of ependymomas that include a posterior fossa tumor, a supratentorial tumor, and a pediatric tumor. These different groups have substantial genetic alterations, and also distinct demography, clinical characteristics, and prognosis. This article is intended to review the diverse molecular and genetic aberrations that may be helpful in prognostication and prediction of survival in patients suffering from an ependymoma.
室管膜瘤是一种罕见的神经胶质肿瘤,起源于神经轴的不同部位。在接受最佳治疗后,不同部位肿瘤的临床表现和生存率存在显著差异,这表明它们在肿瘤发生过程中存在内在的分子和基因差异。已确定了一些基因畸变,以明确表征室管膜瘤的不同亚组,包括后颅窝肿瘤、幕上肿瘤和儿童肿瘤。这些不同的组具有大量的基因改变,以及不同的人口统计学、临床特征和预后。本文旨在综述各种分子和基因畸变,这些畸变可能有助于室管膜瘤患者的预后评估和生存预测。