Genomic‐based ancillary assays offer improved diagnostic yield of effusion cytology with potential challenges in malignant pleural mesothelioma
Genomic‐based ancillary assays offer improved diagnostic yield of effusion cytology with potential challenges in malignant pleural mesothelioma
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基于基因组的辅助检测提高了积液细胞学的诊断率,但对恶性胸膜间皮瘤存在潜在挑战
DOI:
10.1111/pin.12973
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发表时间:
2020
影响因子:
2.2
通讯作者:
Nabeshima K
中科院分区:
文献类型:
--
作者:
Kinoshita Y;Hamasaki M;Matsumoto S;Yoshimura M;Sato A;Tsujimura T;Kamei T;Kawahara K;Nabeshima K
BRCA1‐associated protein 1 (BAP1) or methylthioadenosine phosphorylase (MTAP) immunohistochemistry (IHC) or 9p21 fluorescencein situhybridization (FISH) are useful for the diagnosis of malignant pleural mesothelioma (MPM). However, the effect of these assays on the diagnostic yield of effusion cytology in MPM cases with suspicious cytomorphology or the diagnostic challenges in BAP1 or MTAP IHC have not been fully elucidated. Two cohorts of cytologic preparations obtained from pleural effusions were examined: MPM cases in cohort 1 were used to evaluate whether BAP1 or MTAP IHC or 9p21 FISH increase the diagnostic yield of effusion cytology; cohort 2 included cases suspicious for MPM, to which BAP1 or MTAP IHC was applied to clarify the challenges in the clinical assessment of these assays. In cohort 1 (n= 28), either assay elevated 62.5% of class II or III cases to class V. In cohort 2 (n= 139), 21.7% of BAP1 immunocytochemistry in smears and 10.6% of BAP1 IHC and 9.4% of MTAP IHC in cell blocks, were identified to be challenging. The application of genomic‐based assays increased the diagnostic yield of effusion cytology in the diagnosis of MPM. However, diagnostic challenges limit the application of these assays in some cases.
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影响因子:
3.3
作者:
D. Ospina;V. Villegas;Giovanni Rodríguez;Milena Rondón
通讯作者:
Milena Rondón
影响因子:
5.6
作者:
Hwang, Harry;Tse, Christopher;Churg, Andrew
通讯作者:
Churg, Andrew
DOI:
10.1038/modpathol.2015.87
发表时间:
2015-10
期刊:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
影响因子:
--
作者:
Andrici J;Sheen A;Sioson L;Wardell K;Clarkson A;Watson N;Ahadi MS;Farzin M;Toon CW;Gill AJ
通讯作者:
Gill AJ
影响因子:
5.6
作者:
Sheffield, Brandon S.;Hwang, Harry C.;Churg, Andrew
通讯作者:
Churg, Andrew
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
B. Garcia
通讯作者:
B. Garcia