Sutherland G R, Florell R, Louw D, Choi N W, Sima A A
Department of Pharmacology, Health Sciences Centre, University of Manitoba, Winnipeg.
Can J Neurol Sci. 1987 Nov;14(4):586-92.
The incidence of primary intracranial tumors in Manitoba, Canada was reviewed. From 1980 through 1985, 657 tumors were diagnosed. The crude incidence rates were 10.2/100,000 for males and 10.8/100,000 for females. The three most common tumors were: astrocytoma 281 (43%), meningioma 145 (22%), and pituitary adenoma 111 (17%). Average annual incidence rates for all tumors showed a bimodal distribution with one peak in the 0-4 age group (4.2/100,000), and the other in the 60-69 age group (27.2/100,000). For malignant astrocytoma, the age-specific annual incidence rate increased to the seventh decade where it reached a peak of 14.3/100,000. The incidence of benign astrocytoma remained relatively constant with age at 1.1/100,000. The annual incidence of meningioma increased with age up to the eighth decade reaching 7.2/100,000. Of the 145 meningiomas, 56 (39%) were meningotheliomatous, 48 (33%) transitional, 10 (7%) malignant, 7 (5%) fibroblastic, 6 (4%) psammomatous, 3 (2%) angioblastic, and 15 (10%) lacked pathologic diagnosis. The annual incidence of pituitary adenoma showed two peaks, the first occurring in the third decade (2.6/100,000) and the second in the eighth decade (3.2/100,000). Although the incidence of meningioma was relatively high, the clinical features and pathologic patterns of these tumors were not unlike those previously reported in the literature.
对加拿大曼尼托巴省原发性颅内肿瘤的发病率进行了回顾性研究。1980年至1985年期间,共诊断出657例肿瘤。男性的粗发病率为10.2/10万,女性为10.8/10万。三种最常见的肿瘤为:星形细胞瘤281例(43%)、脑膜瘤145例(22%)和垂体腺瘤111例(17%)。所有肿瘤的年均发病率呈双峰分布,一个高峰在0 - 4岁年龄组(4.2/10万),另一个在60 - 69岁年龄组(27.2/10万)。对于恶性星形细胞瘤,年龄特异性年均发病率在七十年代达到最高,为14.3/10万。良性星形细胞瘤的发病率随年龄保持相对稳定,为1.1/10万。脑膜瘤的年均发病率随年龄增长至八十年代达到7.2/10万。在145例脑膜瘤中,56例(39%)为脑膜皮型,48例(33%)为过渡型,10例(7%)为恶性,7例(5%)为纤维母细胞型,6例(4%)为砂粒体型,3例(2%)为血管母细胞型,15例(10%)缺乏病理诊断。垂体腺瘤的年均发病率有两个高峰,第一个出现在三十年代(2.6/10万),第二个出现在八十年代(3.2/10万)。虽然脑膜瘤的发病率相对较高,但这些肿瘤的临床特征和病理类型与文献中先前报道的并无不同。