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[德国间皮瘤登记处:当前的病理诊断与服务]

[The German Mesothelioma Register : Current pathological diagnostics and services].

作者信息

Feder I S, Jülich M, Tannapfel A, Tischoff I

机构信息

Georgius Agricola Stiftung Ruhr, Deutsches Mesotheliomregister, Institut für Pathologie, Ruhr-Universität Bochum, Bürkle-de-la-Camp Platz 1, 44789, Bochum, Deutschland.

出版信息

Pathologe. 2018 Dec;39(Suppl 2):241-246. doi: 10.1007/s00292-018-0509-8.

Abstract

BACKGROUND

In Germany, asbestos-related diseases (asbestosis, lung cancer, mesothelioma) are recognised and compensated occupational diseases. The histologic diagnosis of mesothelioma is sometimes a challenge; additional immunohistochemical and molecular methods are needed. With lung dust analysis, the current asbestos fibre burden of the lung is measured (biomonitoring). Identification of grade I asbestosis (minimal asbestosis) requires directed histological examinations with up to 400-fold magnification, additional iron staining and possibly in connection with a lung dust analysis.

OBJECTIVES

Demonstration of current pathologic diagnostics in association with mesothelioma and lung dust analysis.

MATERIALS AND METHODS

Analysis of routine data from the German Mesothelioma Register.

RESULTS

Contrary to reactive mesothelial hyperplasia, malignant mesotheliomas have a nuclear BAP1 loss-of-expression in up to 66% of cases. For differential diagnosis between reactive versus malignant, a p16-FISH test may be helpful. BAP1 loss-of-expression and p16-deletion are independent markers. Evaluation of the dataset of the German Mesothelioma Register of patients with repeated tissue sampling proves the detection of asbestos fibres at the same level even after 40 years. The asbestos fibre burden in the human lung remains stable over this long period of time. In the electron microscopic analysis, white asbestos was predominantly found.

CONCLUSIONS

The well-known and industrially appreciated characteristics of asbestos fibres (in ancient ἄσβεστος asbestos "imperishable") as biopersistent have also been experimentally confirmed in human lungs.

摘要

背景

在德国,与石棉相关的疾病(石棉肺、肺癌、间皮瘤)被认定为可获赔偿的职业病。间皮瘤的组织学诊断有时颇具挑战;需要借助额外的免疫组化和分子方法。通过肺尘埃分析可测量肺部当前的石棉纤维负荷(生物监测)。识别I级石棉肺(轻度石棉肺)需要进行放大倍数高达400倍的定向组织学检查、额外的铁染色,可能还需结合肺尘埃分析。

目的

展示与间皮瘤及肺尘埃分析相关的当前病理诊断方法。

材料与方法

分析德国间皮瘤登记处的常规数据。

结果

与反应性间皮增生相反,高达66%的恶性间皮瘤病例存在核BAP1表达缺失。对于反应性与恶性的鉴别诊断,p16-FISH检测可能会有所帮助。BAP1表达缺失和p16缺失是独立的标志物。对德国间皮瘤登记处有重复组织采样的患者数据集进行评估,结果表明即使在40年后仍能检测到相同水平的石棉纤维。在如此长的时间里,人类肺部的石棉纤维负荷保持稳定。在电子显微镜分析中,主要发现的是白石棉。

结论

石棉纤维广为人知且在工业上备受重视的特性(在古代希腊语中ἄσβεστος意为“不朽的”石棉,即生物持久性)在人体肺部也得到了实验证实。

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