Cozzi Ilaria, Oprescu Florina Anca, Rullo Emma, Ascoli Valeria
Department of Radiological, Oncological and Anatomo-Pathological Sciences, Sapienza University, Viale Regina, Rome 324-00161, Italy.
Diagn Cytopathol. 2018 Jan;46(1):9-14. doi: 10.1002/dc.23837. Epub 2017 Oct 10.
The important diagnostic challenge facing the cytopathologist is whether a mesothelial proliferation on effusions represents a malignant mesothelioma (MM) or a benign mesothelial hyperplasia (MH). Here, we evaluated the diagnostic utility of BAP1 immunohistochemistry (IHC) in distinguishing between reactive and neoplastic mesothelial cells.
In pleural and peritoneal effusions from 147 patients with diagnosed MM or with a differential diagnosis of MM and MH, the expression of BAP1 was examined by IHC on paraffin-embedded cell blocks (n = 121) and biopsies (n = 44). Included were also synchronous and methacronous cytology/biopsy pair samples. BAP1 IHC was evaluated for nuclear staining as positive or negative on target mesothelial cells, with appropriate internal control.
In MM cases, loss of BAP1 nuclear staining was observed in 76.5% of the cell blocks and 47.5% of the biopsies. All BAP1-negative cases with a differential diagnosis of benign and malignant mesothelial proliferations were MM at follow-up. All MH cases, the 29% of epithelial MM and the 90% of nonepithelial MM, retained BAP1 expression. Synchronous and methacronous biopsy/cytology pairs showed matching BAP1 results.
In effusions with mesotheliomatous cells or atypical mesothelial cells of uncertain significance, negative BAP1 IHC strongly supports a diagnosis of MM. With prudence in interpreting immunostaining, BAP1 may be included in IHC panels for MM cytodiagnosis, given its high specificity and sensitivity.
细胞病理学家面临的重要诊断挑战是,积液中的间皮细胞增殖是代表恶性间皮瘤(MM)还是良性间皮增生(MH)。在此,我们评估了BAP1免疫组化(IHC)在区分反应性和肿瘤性间皮细胞方面的诊断效用。
在147例已确诊MM或鉴别诊断为MM和MH的患者的胸腔和腹腔积液中,通过免疫组化在石蜡包埋细胞块(n = 121)和活检标本(n = 44)上检测BAP1的表达。还纳入了同步和异时的细胞学/活检配对样本。在有适当内部对照的情况下,对目标间皮细胞的BAP1免疫组化进行核染色评估,判断为阳性或阴性。
在MM病例中,76.5%的细胞块和47.5%的活检标本中观察到BAP1核染色缺失。所有鉴别诊断为良性和恶性间皮细胞增殖的BAP1阴性病例在随访时均为MM。所有MH病例、29%的上皮性MM和90%的非上皮性MM均保留BAP1表达。同步和异时的活检/细胞学配对显示BAP1结果匹配。
在含有间皮瘤细胞或意义不确定的非典型间皮细胞的积液中,BAP1免疫组化阴性强烈支持MM的诊断。鉴于其高特异性和敏感性,在谨慎解读免疫染色结果的情况下,BAP1可纳入MM细胞诊断的免疫组化检测组合中。