BAP-1 in the diagnosis of malignant pleural mesothelioma

IF 2.1 4区 医学 Q3 RESPIRATORY SYSTEM
Respiratory Medicine and Research Pub Date : 2026-05-01 Epub Date: 2025-11-28 DOI:10.1016/j.resmer.2025.101231
Irene Sansano , Ana Vázquez , Oscar Persiva , Marc Simó , Leire Sánchez , Pilar Montoya , Carme Dinarès , Carmen Alemán
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引用次数: 0

Abstract

Background

The diagnosis of malignant pleural mesothelioma (MPM) can be challenging for clinicians and pathologists.

Patients and methods

This study included all patients diagnosed with pleural mesothelioma between October 2013 and April 2024. Clinical data, history of asbestos exposure, pleural fluid analysis, chest-X-ray, thoracic computed tomography and positron emission tomography findings, video-assisted thoracic surgery report, pleural fluid cytology and pleural biopsy results were included. Loss of BRCA1-associated protein 1 (BAP1) nuclear staining was examined in cytologies and biopsies.

Results

Forty-one patients were diagnosed with pleural mesothelioma, 35 epithelioid, 5 sarcomatoid and 1 biphasic. The diagnosis was established after the first sample in 30 patients, while a second one was necessary in 11 patients. BAP1 loss in pleural cytology and histology was not always consistent. Sixteen patients showed loss of BAP1 expression in cytology. Among these, 10 patients also presented BAP1 loss in pleural histology, whereas 5 patients with BAP1 loss in histology did not show BAP1 loss in cytology. Additionally, two patients initially diagnosed with idiopathic pleural effusion and 3 patients diagnosed with benign pleural effusion due to asbestos showed BAP1 loss and were later diagnosed with MPM during follow-up.

Conclusion

MPM remains difficult to diagnose. Performing BAP1 immunohistochemistry in patients with an undiagnosed pleural effusion or a history of asbestos exposure can aid in identifying those with mesothelioma.
BAP-1在恶性胸膜间皮瘤中的诊断价值。
背景:恶性胸膜间皮瘤(MPM)的诊断对临床医生和病理学家来说是具有挑战性的。患者和方法:本研究纳入2013年10月至2024年4月期间诊断为胸膜间皮瘤的所有患者。包括临床资料、石棉接触史、胸膜液分析、胸部x线、胸部计算机断层扫描和正电子发射断层扫描结果、胸腔镜手术报告、胸膜液细胞学检查和胸膜活检结果。细胞学和活组织检查brca1相关蛋白1 (BAP1)核染色缺失。结果:胸膜间皮瘤41例,上皮样瘤35例,肉瘤样瘤5例,双相瘤1例。30名患者在第一次取样后确诊,11名患者需要进行第二次取样。胸膜细胞学和组织学的BAP1缺失并不总是一致的。16例患者细胞学显示BAP1表达缺失。其中10例患者胸膜组织学上也出现BAP1丢失,5例组织学上BAP1丢失的患者细胞学上未出现BAP1丢失。另外,2例最初诊断为特发性胸腔积液的患者和3例诊断为石棉所致良性胸腔积液的患者均出现BAP1丢失,并在随访中被诊断为MPM。结论:MPM仍然难以诊断。对未确诊胸腔积液或石棉暴露史的患者进行BAP1免疫组化检查有助于间皮瘤患者的鉴别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Medicine and Research
Respiratory Medicine and Research RESPIRATORY SYSTEM-
CiteScore
2.70
自引率
0.00%
发文量
82
审稿时长
50 days
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