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Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions

BACKGROUND: One of the problems in studying serous effusion cytological samples is differentiation of reactive mesothelial cells from metastatic adenocarcinoma cells. MATERIALS AND METHODS: In this study, the immunohistochemical diagnostic value of E-cadherin and fibronectin markers for differentiat...

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Autores principales: Moghaddam, Noushin Afshar, Tahririan, Reza, Eftekhari, Mehdi, Tahririan, Dana, Rahmani, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544133/
https://www.ncbi.nlm.nih.gov/pubmed/23326787
http://dx.doi.org/10.4103/2277-9175.100173
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author Moghaddam, Noushin Afshar
Tahririan, Reza
Eftekhari, Mehdi
Tahririan, Dana
Rahmani, Alireza
author_facet Moghaddam, Noushin Afshar
Tahririan, Reza
Eftekhari, Mehdi
Tahririan, Dana
Rahmani, Alireza
author_sort Moghaddam, Noushin Afshar
collection PubMed
description BACKGROUND: One of the problems in studying serous effusion cytological samples is differentiation of reactive mesothelial cells from metastatic adenocarcinoma cells. MATERIALS AND METHODS: In this study, the immunohistochemical diagnostic value of E-cadherin and fibronectin markers for differentiation of these 2 groups of cells was studied. 50 cell block samples prepared from serous effusions were examined. Based on clinical and histological studies, 25 cases had primary carcinoma, and the other 25 were proved to be benign effusion cases. All the cases were studied for E-cadherin and fibronectin immunostaining using an envision technique. Statistical analyzes were performed employing Chi-square and exact Fisher tests, using SPSS software (version 16). RESULTS: 24 of the 25 benign cases were stained with fibronectin and 2 with E-cadherin, whereas from among the 25 metastatic cases, 2 reacted to fibronectin and 22 to E-cadherin. Considering the staining of the 2 markers under conditions that the cells were stained with fibronectin but not with E-cadherin, positive predictive value (PPV) and negative predictive value (NPV) to identify reactive mesothelial cells were 100% and 92.5% while under conditions that had not been stained with fibronectin but with E-cadherin, PPV and NPV to detect adenocarcinoma cells were 95.2% and 82.1%, respectively. CONCLUSION: Employing this short panel can be helpful for better differentiation of adenocarcinoma and reactive mesothelial cells in serous fluids.
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spelling pubmed-35441332013-01-16 Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions Moghaddam, Noushin Afshar Tahririan, Reza Eftekhari, Mehdi Tahririan, Dana Rahmani, Alireza Adv Biomed Res Original Article BACKGROUND: One of the problems in studying serous effusion cytological samples is differentiation of reactive mesothelial cells from metastatic adenocarcinoma cells. MATERIALS AND METHODS: In this study, the immunohistochemical diagnostic value of E-cadherin and fibronectin markers for differentiation of these 2 groups of cells was studied. 50 cell block samples prepared from serous effusions were examined. Based on clinical and histological studies, 25 cases had primary carcinoma, and the other 25 were proved to be benign effusion cases. All the cases were studied for E-cadherin and fibronectin immunostaining using an envision technique. Statistical analyzes were performed employing Chi-square and exact Fisher tests, using SPSS software (version 16). RESULTS: 24 of the 25 benign cases were stained with fibronectin and 2 with E-cadherin, whereas from among the 25 metastatic cases, 2 reacted to fibronectin and 22 to E-cadherin. Considering the staining of the 2 markers under conditions that the cells were stained with fibronectin but not with E-cadherin, positive predictive value (PPV) and negative predictive value (NPV) to identify reactive mesothelial cells were 100% and 92.5% while under conditions that had not been stained with fibronectin but with E-cadherin, PPV and NPV to detect adenocarcinoma cells were 95.2% and 82.1%, respectively. CONCLUSION: Employing this short panel can be helpful for better differentiation of adenocarcinoma and reactive mesothelial cells in serous fluids. Medknow Publications & Media Pvt Ltd 2012-08-28 /pmc/articles/PMC3544133/ /pubmed/23326787 http://dx.doi.org/10.4103/2277-9175.100173 Text en Copyright: © 2012 Moghaddam http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Moghaddam, Noushin Afshar
Tahririan, Reza
Eftekhari, Mehdi
Tahririan, Dana
Rahmani, Alireza
Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
title Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
title_full Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
title_fullStr Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
title_full_unstemmed Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
title_short Diagnostic value of E-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
title_sort diagnostic value of e-cadherin and fibronectin in differentiation between reactive mesothelial and adenocarcinoma cells in serous effusions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544133/
https://www.ncbi.nlm.nih.gov/pubmed/23326787
http://dx.doi.org/10.4103/2277-9175.100173
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