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少突胶质细胞瘤的分子病理学

Molecular pathology of oligodendroglial tumors.

作者信息

Hartmann Christian, von Deimling Andreas

机构信息

Universitätsklinikum Heidelberg Pathologisches Institut, Abt. Neuropathologie, Heidelberg, Germany.

出版信息

Recent Results Cancer Res. 2009;171:25-49. doi: 10.1007/978-3-540-31206-2_2.

Abstract

The term oligodendroglioma was created by Bailey, Cushing, and Bucy based on the observation that these tumors share morphological similarities with oligodendrocytes (Bailey and Cushing 1926; Bailey and Bucy 1929). However, a convincing link between oligodendrocytes and oligodendrogliomas still needs to be shown. Oligoastrocytomas or mixed gliomas are histologically defined by the presence of oligodendroglial and astrocytic components. According to the WHO classification of brain tumors, oligodendroglial tumors are separated into oligodendrogliomas WHO grade II (OII), anaplastic oligodendrogliomas WHO grade III (OIII), oligoastrocytomas WHO grade II (OAII), anaplastic oligoastrocytomas WHO grade III (OAIII), and glioblastomas with oligodendroglioma component WHO grade IV (GBMo) (Louis et al. 2007).The perception of oligodendroglial tumors has changed in recent years. The diagnosis of oligodendroglioma or oligoastrocytomas is made much more frequently than 10 years ago. Treatment modalities have been advanced and novel concepts regarding the origin of oligodendroglial tumors have been developed. This review focuses on recent developments with impact on the diagnosis and understanding of molecular mechanisms in oligodendroglial tumors.

摘要

少突胶质细胞瘤这一术语由贝利、库欣和布西提出,是基于这些肿瘤与少突胶质细胞在形态学上具有相似性的观察结果(贝利和库欣,1926年;贝利和布西,1929年)。然而,少突胶质细胞与少突胶质细胞瘤之间令人信服的联系仍有待证实。少突星形细胞瘤或混合性胶质瘤在组织学上由少突胶质细胞和星形细胞成分的存在来定义。根据世界卫生组织(WHO)的脑肿瘤分类,少突胶质细胞肿瘤分为WHO二级少突胶质细胞瘤(OII)、WHO三级间变性少突胶质细胞瘤(OIII)、WHO二级少突星形细胞瘤(OAII)、WHO三级间变性少突星形细胞瘤(OAIII)以及WHO四级具有少突胶质细胞瘤成分的胶质母细胞瘤(GBMo)(路易斯等人,2007年)。近年来,对少突胶质细胞肿瘤的认识发生了变化。少突胶质细胞瘤或少突星形细胞瘤的诊断比10年前更为常见。治疗方式得到了改进,并且已经形成了关于少突胶质细胞肿瘤起源的新观念。本综述重点关注对少突胶质细胞肿瘤诊断和分子机制理解有影响的最新进展。

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