Hiroshima Kenzo, Wu Di, Hasegawa Mizue, Koh Eitetsu, Sekine Yasuo, Ozaki Daisuke, Yusa Toshikazu, Walts Ann E, Marchevsky Alberto M, Nabeshima Kazuki, Tada Yuji, Shimada Hideaki, Tagawa Masatoshi
Department of Pathology, Tokyo Women's Medical University, Yachiyo Medical Center, Yachiyo, Japan.
Department of Respirology, Tokyo Women's Medical University, Yachiyo Medical Center, Yachiyo, Japan.
Diagn Cytopathol. 2016 Jul;44(7):591-8. doi: 10.1002/dc.23490. Epub 2016 Apr 15.
Mesothelioma patients often present with serosal effusions, which are ideal for cytopathological diagnoses. However, the morphological overlap between malignant and benign mesothelial proliferation can make a conclusive cytological diagnosis of mesothelioma elusive because immunohistochemical staining does not discriminate definitively between the two in this setting. p16 is deleted in up to 80% of pleural mesotheliomas. The aim of this study was to establish the correlation between the p16 deletion status of the cell block with that of its corresponding tumor using fluorescence in situ hybridization (FISH) analysis for individual patient tumors.
Twenty-two biopsies and 24 corresponding cell blocks, containing serosal effusions with atypical mesothelial cells from 22 patients with histologically confirmed pleural mesotheliomas, were analyzed with p16 FISH. Seventeen cell blocks consisting of serosal effusions with reactive mesothelial cells from nonmesothelioma cases were also analyzed. Combined immunofluorescence and FISH were also performed.
Seventeen of the 22 mesothelioma patients (77.3%) showed homozygous deletions of p16 in the tumor tissue and in the atypical mesothelial cells from the cell blocks. p16 FISH followed by immunofluorescence with EMA was helpful towards identifying the mesothelioma cells in the cell blocks.
We confirmed that the p16 FISH results obtained from the cell blocks are as reliable as those from the tissue sections. Cell block analysis is recommended for patients with serosal effusions of unknown origins with the following methods: immunohistochemistry should be performed to validate the mesothelial origin, and p16 FISH should be performed to confirm malignancy. Diagn. Cytopathol. 2016;44:591-598. © 2016 Wiley Periodicals, Inc.
间皮瘤患者常伴有浆膜腔积液,这是细胞病理学诊断的理想样本。然而,恶性和良性间皮细胞增生在形态学上存在重叠,这使得间皮瘤的确定性细胞学诊断难以实现,因为在这种情况下免疫组化染色无法明确区分两者。高达80%的胸膜间皮瘤存在p16基因缺失。本研究的目的是通过荧光原位杂交(FISH)分析个体患者肿瘤,确定细胞块中p16基因缺失状态与其相应肿瘤的p16基因缺失状态之间的相关性。
对22例经组织学确诊的胸膜间皮瘤患者的22份活检标本和24份相应的细胞块进行p16 FISH分析,这些细胞块包含有非典型间皮细胞的浆膜腔积液。还对17份由非间皮瘤病例的反应性间皮细胞组成的浆膜腔积液细胞块进行了分析。同时进行了联合免疫荧光和FISH检测。
22例间皮瘤患者中有17例(77.3%)在肿瘤组织和细胞块中的非典型间皮细胞中显示出p16基因纯合缺失。先进行p16 FISH,然后用EMA进行免疫荧光检测,有助于识别细胞块中的间皮瘤细胞。
我们证实从细胞块获得的p16 FISH结果与从组织切片获得的结果一样可靠。对于来源不明的浆膜腔积液患者,建议采用以下方法进行细胞块分析:应进行免疫组化以验证间皮来源,应进行p16 FISH以确认恶性肿瘤。诊断细胞病理学。2016;44:591 - 598。©2016威利期刊公司。