Gilles F H, Sobel E L, Tavaré C J, Leviton A, Hedley-Whyte E T
Department of Pathology, University of Southern California School of Medicine, Los Angeles, USA.
Neurosurgery. 1995 Dec;37(6):1056-68. doi: 10.1227/00006123-199512000-00004.
In the Childhood Brain Tumor Consortium database, the proportions of older children (> or = 11 yr) with pilocytic astrocytomas, fibrillary astrocytomas, and ependymomas significantly increased (P < 0.05) over the 50 years (1930-1979) of the study. The increased proportions of pilocytic astrocytomas occurred whether the tumors were located in the supratentorial or infratentorial compartments. The increases in fibrillary astrocytomas and ependymomas were found only within the supratentorial tumor location. Some histological features found in pilocytic astrocytomas (e.g., Rosenthal fibers, granular bodies, and very low cell density) were more likely to be found in older children. Other histological features were also more likely to be found in older children (e.g., parenchymal calcification, intertwined fascicles, intermediate and large-size nuclei, pleomorphic, elongated, or irregular nuclei, prominent nucleoli, multinucleated cells, thick hyaline blood vessels, hemosiderin, and parenchymal and perivascular lymphocytes). The probability of 5-year survival for young children with supratentorial ependymomas remained at approximately 0.4 in contrast to that for young children with infratentorial ependymomas, for whom it improved, but without significant linear trend. The probability of 5-year survival for both younger and older children with primitive neuroectodermal tumors (medulloblastomas) improved, but without significant linear trend. The changes in the proportions of childhood brain tumors and histological features occurred without similar changes in the proportions of older and younger children in the cities involved between 1930 and 1979. These changes were so distinctive as to raise the possibility of significant shifts in environmental exposures in younger and older children over the 50 years of this study.
在儿童脑肿瘤协会数据库中,在长达50年(1930 - 1979年)的研究期间,年龄较大儿童(≥11岁)患毛细胞型星形细胞瘤、纤维型星形细胞瘤和室管膜瘤的比例显著增加(P < 0.05)。无论肿瘤位于幕上还是幕下区域,毛细胞型星形细胞瘤的比例均有所增加。纤维型星形细胞瘤和室管膜瘤比例的增加仅见于幕上肿瘤部位。在毛细胞型星形细胞瘤中发现的一些组织学特征(如罗斯enthal纤维、颗粒体和极低的细胞密度)在年龄较大儿童中更易出现。其他组织学特征在年龄较大儿童中也更易出现(如实质钙化、交织的束状结构、中等大小和大尺寸细胞核、多形性、细长或不规则细胞核、明显核仁、多核细胞、厚的透明血管、含铁血黄素以及实质和血管周围淋巴细胞)。幕上室管膜瘤幼儿的5年生存率约为0.4,而幕下室管膜瘤幼儿的5年生存率有所提高,但无显著线性趋势。原始神经外胚层肿瘤(髓母细胞瘤)患儿无论年龄大小,5年生存率均有所提高,但无显著线性趋势。1930年至1979年间,所涉城市中年龄较大和较小儿童的比例未发生类似变化,而儿童脑肿瘤比例和组织学特征却发生了改变。这些变化非常显著,以至于增加了在本研究的50年期间幼儿和年长儿童环境暴露发生重大变化的可能性。