From the Department of Cellular Pathology, Cardiff and Vale University Health Board, and Cardiff University, University Hospital of Wales, Cardiff, United Kingdom (Drs Attanoos and Gibbs); the Department of Pathology and Laboratory Medicine, University of British Columbia, and Vancouver General Hospital, Vancouver, British Columbia, Canada (Dr Churg); the Department of Biopathology, Léon-Bérard Cancer Centre, Lyon, France (Dr Galateau-Salle); and the Department of Pathology, Duke University Medical Center, Durham, North Carolina (Dr Roggli).
Arch Pathol Lab Med. 2018 Jun;142(6):753-760. doi: 10.5858/arpa.2017-0365-RA. Epub 2018 Feb 26.
CONTEXT: - Although many mesotheliomas are related to asbestos exposure, not all are, and there is increasing information on other causes of mesothelioma. OBJECTIVE: - To provide a review of non-asbestos causes for malignant mesothelioma. DATA SOURCES: - Review of relevant published literature via PubMed and other search engines. CONCLUSIONS: - Currently, most pleural mesotheliomas (70% to 90%) in men in Europe and North America are attributable to asbestos exposure; for peritoneal mesothelioma the proportion is lower. In North America few mesotheliomas in women at any site are attributable to asbestos exposure, but in Europe the proportion is higher and varies considerably by locale. In certain geographic locations other types of mineral fibers (erionite, fluoro-edenite, and probably balangeroite) can induce mesothelioma. Therapeutic radiation for other malignancies is a well-established cause of mesothelioma, with relative risks as high as 30. Carbon nanotubes can also induce mesotheliomas in animals but there are no human epidemiologic data that shed light on this issue. Chronic pleural inflammation may be a cause of mesothelioma but the data are scanty. Although SV40 can induce mesotheliomas in animals, in humans the epidemiologic data are against a causative role. A small number of mesotheliomas (probably in the order of 1%) are caused by germline mutations/deletions of BRCA1-associated protein-1 ( BAP1) in kindreds that also develop a variety of other cancers. All of these alternative etiologies account for a small proportion of tumors, and most mesotheliomas not clearly attributable to asbestos exposure are spontaneous (idiopathic).
背景:- 虽然许多间皮瘤与石棉暴露有关,但并非所有间皮瘤都是如此,并且关于间皮瘤的其他病因的信息正在不断增加。 目的:- 综述恶性间皮瘤的非石棉病因。 数据来源:- 通过 PubMed 和其他搜索引擎对相关已发表文献进行综述。 结论:- 目前,欧洲和北美的大多数胸膜间皮瘤(70%至 90%)可归因于石棉暴露;而腹膜间皮瘤的比例较低。在北美,几乎没有任何部位的女性间皮瘤可归因于石棉暴露,但在欧洲,这一比例较高,且因地区而异。在某些地理位置,其他类型的矿物纤维(蓝石棉、氟-伊腾石和可能的巴朗盖罗石)可诱发间皮瘤。其他恶性肿瘤的治疗性放射是间皮瘤的一个明确病因,相对风险高达 30。碳纳米管也可在动物中诱发间皮瘤,但尚无人类流行病学数据阐明这一问题。慢性胸膜炎症可能是间皮瘤的一个病因,但数据很少。尽管 SV40 可在动物中诱发间皮瘤,但在人类中,流行病学数据表明其无致病作用。少数间皮瘤(可能为 1%左右)是由家族性 BRCA1 相关蛋白-1(BAP1)的种系突变/缺失引起的,这些家族还会发生多种其他癌症。所有这些替代病因仅占肿瘤的一小部分,大多数与石棉暴露无关的间皮瘤是自发性的(特发性的)。
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