Ahmed Naseem, Bhurgri Yasmin, Sadiq Saleem, Shakoor Kazi A
Department of Pathology, Basic Medical Sciences Institute, Karachi.
Asian Pac J Cancer Prev. 2007 Jul-Sep;8(3):399-404.
The objectives of this study were to determine the epidemiology of brain tumors during infancy and childhood and to define and segregate childhood brain tumors vis-a-vis their morphological characteristics. The present study includes pediatric brain tumors, ICD-10 category C71 encountered during 10 years (January 1989 through December 1998) at a tertiary care hospital in Karachi. Eighty one cases were included, 58 (71.6%) in males and 23 (28.4%) in females with a male to female ratio of 2.5:1. The cases were divided into 3 age groups each covering five years of life (0-4, 5-9, 10-14 years), with the greatest number in the second age group i.e. 5-9 years followed by the third age group and the 0-4 year age group. The mean age for all cases, both genders was 8.8 years (95% CI 7.9; 9.6) with a marginal variation for cases occurring in the cerebrum and cerebellum. The malignancies occurred at a younger age in the males for each subcategory by site and morphology. The morphological distribution of cases was astrocytoma (28 cases, 34.6%), primitive neuroectodermal tumor or PNET (40 cases; 49.4%), ependymoma (8 cases, 10%), mixed glioma (4 cases; 5%) and a case of oligodendroglioma. The 81 malignancies included in this study were further categorized by site into two groups, supratentorial (27 cases; 33.3%) and infratentorial (54 cases; 66.7%). The morphological categorization of supratentorial tumors was astrocytoma (17 cases; 63%), ependymoma (5 cases; 18.5%), mixed glioma (2 cases; 7.4%). PNET with rhabdoid differentiation, oligodendroglioma and pinealoblastoma comprised 1 case (3.7%) each. The 17 supratentorial astrocytoma were sub-categorized as follows - pilocytic astrocytoma (5 cases; 29.4%), grade II astrocytoma (6 cases; 35.3%); grade III astrocytoma (2 cases; 11.8%), anaplastic astrocytoma (1 case; 5.9%) and glioblastoma multiforme (3 cases; 17.7%). The morphological categorization of infratentorial tumors was astrocytoma (11 cases; 20.4%), medulloblastoma (38 cases; 70.4%), ependymoma (3 cases; 5.6%) and mixed glioma - astroependymoma (2 cases, 3.7%). The morphological sub-categorization of infratentorial astrocytoma was pilocytic astrocytoma (7 cases, 63.6%), with gemistocytic astrocytoma, grade II, grade III and anaplastic astrocytoma comprising 1 (9.1%) case each. The morphological categorization of medulloblastoma was classical medulloblastoma (15 cases; 39.5%), desmoplastic medulloblastoma (8 cases; 21.1%), medulloblastoma with astrocytic differentiation (12 cases; 31.5%), medulloblastoma with neural differentiation (2 cases; 5.3%), and neuroblastic medulloblastoma (1 case; 2.6%). The pediatric brain tumors in Karachi reflect a developing country scenario, with a strong male predisposition and a late presentation with a peak in the 5-9 year age group. There is a predominance of medulloblastoma and a paucity of astrocytomas. The current study is a single institution study and needs cautious interpretation. Population-based studies are required to determine the cancer burden due to pediatric malignancies of the brain in this population and for the morphological categorization of brain tumors in Karachi.
本研究的目的是确定婴幼儿及儿童期脑肿瘤的流行病学特征,并根据其形态学特征对儿童脑肿瘤进行定义和分类。本研究纳入了卡拉奇一家三级护理医院在10年期间(1989年1月至1998年12月)遇到的儿科脑肿瘤,即国际疾病分类第10版C71类疾病。共纳入81例病例,其中男性58例(71.6%),女性23例(28.4%),男女比例为2.5:1。病例分为3个年龄组,每组涵盖5岁年龄段(0 - 4岁、5 - 9岁、10 - 14岁),其中第二年龄组(即5 - 9岁)病例数最多,其次是第三年龄组和0 - 4岁年龄组。所有病例(无论性别)的平均年龄为8.8岁(95%可信区间7.9;9.6),大脑和小脑肿瘤病例的年龄略有差异。按部位和形态学分类,各亚类男性恶性肿瘤发病年龄较轻。病例的形态学分布为星形细胞瘤(28例,34.6%)、原始神经外胚层肿瘤或PNET(40例;49.4%)、室管膜瘤(8例,10%)、混合性胶质瘤(4例;5%)和1例少突胶质细胞瘤。本研究纳入的81例恶性肿瘤按部位进一步分为两组,幕上肿瘤(27例;33.3%)和幕下肿瘤(54例;66.7%)。幕上肿瘤的形态学分类为星形细胞瘤(17例;63%)、室管膜瘤(5例;18.5%)、混合性胶质瘤(2例;7.4%)。具有横纹肌样分化的PNET、少突胶质细胞瘤和松果体母细胞瘤各1例(3.7%)。17例幕上星形细胞瘤进一步细分为:毛细胞型星形细胞瘤(5例;29.4%)、II级星形细胞瘤(6例;35.3%);III级星形细胞瘤(2例;11.8%)间变性星形细胞瘤(1例;5.9%)和多形性胶质母细胞瘤(3例;17.7%)。幕下肿瘤的形态学分类为星形细胞瘤(11例;20.4%)、髓母细胞瘤(38例;70.4%)、室管膜瘤(3例;5.6%)和混合性胶质瘤 - 室管膜星形细胞瘤(2例,3.7%)。幕下星形细胞瘤的形态学细分是毛细胞型星形细胞瘤(7例,63.6%),肥胖细胞型星形细胞瘤、II级、III级和间变性星形细胞瘤各1例(9.1%)。髓母细胞瘤的形态学分类为经典型髓母细胞瘤(15例;39.5%)、促纤维增生型髓母细胞瘤(8例;21.1%)、伴有星形细胞分化的髓母细胞瘤(12例;31.5%)、伴有神经分化的髓母细胞瘤(2例;5.3%)和神经母细胞型髓母细胞瘤(1例;2.6%)。卡拉奇的儿科脑肿瘤反映了发展中国家的情况,男性易患倾向明显,就诊较晚,发病高峰在5 - 9岁年龄组。髓母细胞瘤占优势,星形细胞瘤较少。本研究是一项单机构研究,需要谨慎解读。需要进行基于人群的研究,以确定该人群中儿童脑恶性肿瘤的癌症负担以及卡拉奇脑肿瘤的形态学分类。