Musk A W, Dolin P J, Armstrong B K, Ford J M, de Klerk N H, Hobbs M S
Department of Respiratory Medicine, Sir Charles Gairdner Hospital, Nedlands, WA.
Med J Aust. 1989 Mar 6;150(5):242-3, 246. doi: 10.5694/j.1326-5377.1989.tb136455.x.
Details of patients with malignant mesothelioma that was diagnosed in Australia before 1981 were obtained by searching all possible sources throughout Australia as far into the past as possible and up to and including 1980. The earliest patient with mesothelioma who was identified was diagnosed in Victoria in 1947. By 1980, 535 (81%) men and 123 (19%) women had been diagnosed with the disease; only 14 persons were aged less than 35 years at the time of diagnosis (the youngest person was 15 years of age). The incidence rate in subjects who were 35 years or older at diagnosis was less than 1.0 cases per million person-years until 1964-1968, and then it rose progressively to 15.5 cases per million person-years in 1979-1980. The highest rate (69.7 cases per million person-years) was observed in 65- to 74-year-old men in 1979-1980. The incidence rate in Western Australia was greater than were the rates in other states of Australia after the mid 1960s. Pleural mesotheliomas accounted for 88% of cases in which the site of the tumour was known; peritoneal mesotheliomas accounted for 10% of such cases and "other" sites for 2% of such cases. In 6% of cases the site was not specified. The exposure to asbestos was stated as "definite" in 59% of the cases with a recorded history of exposure: 8% of all the cases in the study had been exposed to crocidolite (blue asbestos) from Wittenoom Gorge in Western Australia. The age at diagnosis of patients with known exposure to asbestos was similar to that in those without known exposure. The increases in the incidence of malignant mesothelioma in Australia follow the published trends in the production and use of the amphibole varieties of asbestos in this country after a lag period of between 20 and 30 years.
通过尽可能追溯澳大利亚过去的所有可能来源,直至1980年,获取了1981年以前在澳大利亚被诊断为恶性间皮瘤的患者的详细信息。最早确诊的间皮瘤患者于1947年在维多利亚州被诊断出来。到1980年,已有535名(81%)男性和123名(19%)女性被诊断出患有这种疾病;诊断时年龄小于35岁的仅有14人(最年轻的为15岁)。在1964 - 1968年之前,诊断时年龄在35岁及以上的人群中,发病率低于每百万人年1.0例,之后逐渐上升至1979 - 1980年的每百万人年15.5例。1979 - 1980年,65至74岁男性的发病率最高(每百万人年69.7例)。20世纪60年代中期以后,西澳大利亚州的发病率高于澳大利亚其他州。在已知肿瘤部位的病例中,胸膜间皮瘤占88%;腹膜间皮瘤占10%,“其他”部位占2%。6%的病例未明确肿瘤部位。在有接触史记录的病例中,59%的病例石棉接触情况被列为“明确”:研究中所有病例的8%曾接触过西澳大利亚州维特努姆峡谷的青石棉(蓝石棉)。已知接触石棉的患者诊断时的年龄与未接触石棉的患者相似。澳大利亚恶性间皮瘤发病率的上升,在滞后20至30年后,与该国公布之角闪石类石棉生产和使用趋势一致。