Fulling K H, Nelson J S
Department of Pathology, Washington University Medical School, St. Louis, MO 63110.
Semin Diagn Pathol. 1984 May;1(2):152-63.
Cerebral astrocytomas are the most common primary central nervous system (CNS) tumors in adults. As a group these tumors are characterized by histologic variability and inconstant prognosis. Nevertheless, microscopic examination of these tumors with identification of certain histologic features provides useful prognostic information. Evidence of anaplasia including necrosis, vascular endothelial proliferation, mitotic activity, cytologic pleomorphism, and foci of increased cellularity, when present in diffusely infiltrating astrocytic gliomas, is associated with aggressive behavior. In particular, the occurrence of tumor necrosis in anaplastic astrocytomas is reliably predictive of a highly unfavorable outcome. Specific histologic subtypes of cerebral astrocytoma with relatively benign course may also be identified. These include juvenile pilocytic astrocytoma, subependymal giant-cell astrocytoma, and, in some cases, pleomorphic xanthoastrocytoma. The critical influence of tumor location and the limitations imposed by potentially nonrepresentative biopsy material must be appreciated when assessing prognosis in cerebral astrocytomas. Prognostic data provided by histologic examination are useful in selecting treatment regimens and for evaluation of newly proposed therapies.
脑星形细胞瘤是成人中最常见的原发性中枢神经系统(CNS)肿瘤。作为一个群体,这些肿瘤具有组织学变异性和预后不恒定的特点。然而,对这些肿瘤进行显微镜检查并识别某些组织学特征可提供有用的预后信息。在弥漫性浸润性星形胶质细胞瘤中出现的间变证据,包括坏死、血管内皮增生、有丝分裂活性、细胞多形性和细胞增多灶,与侵袭性生物学行为相关。特别是,间变性星形细胞瘤中肿瘤坏死的出现可可靠地预测预后极差。也可以识别出具有相对良性病程的脑星形细胞瘤的特定组织学亚型。这些包括青少年毛细胞型星形细胞瘤、室管膜下巨细胞星形细胞瘤,以及在某些情况下的多形性黄色星形细胞瘤。在评估脑星形细胞瘤的预后时,必须认识到肿瘤位置的关键影响以及潜在的非代表性活检材料所带来的局限性。组织学检查提供的预后数据有助于选择治疗方案和评估新提出的治疗方法。