Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma
Introduction: Although cytological examination helps in diagnosis of malignancy in serous effusion, at times it is difficult to differentiate atypical reactive mesothelial cells from adenocarcinoma (AC) cells. To resolve this problem, various ancillary methods have been used. Immunocytochemistry (IC...
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Format: | Article |
Language: | English |
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Wolters Kluwer Medknow Publications
2019-01-01
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Series: | Journal of Cytology |
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Online Access: | http://www.jcytol.org/article.asp?issn=0970-9371;year=2019;volume=36;issue=1;spage=28;epage=31;aulast=Subbarayan |
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author | Devi Subbarayan Jenna Bhattacharya Poonam Rani Bembem Khuraijam Shyama Jain |
author_facet | Devi Subbarayan Jenna Bhattacharya Poonam Rani Bembem Khuraijam Shyama Jain |
author_sort | Devi Subbarayan |
collection | DOAJ |
description | Introduction: Although cytological examination helps in diagnosis of malignancy in serous effusion, at times it is difficult to differentiate atypical reactive mesothelial cells from adenocarcinoma (AC) cells. To resolve this problem, various ancillary methods have been used. Immunocytochemistry (ICC) is one such commonly used technique in which various panel of antibodies has been tried. Unfortunately, so far no unique marker is available to solve this issue. Hence, the present study evaluates the efficacy of four antibody panel comprising of MOC-31, epithelial membrane antigen (EMA), calretinin (CAL), and mesothelin (MES) to solve this problem. Materials and Methods: Forty-two cases suspected of malignant effusion in pleural/peritoneal fluid and 42 cases of reactive effusion were included. Cytospin smears were prepared and stained with Giemsa stain for cytomorphological diagnosis. Cytospin smears and cell blocks were made forICC. ICC for MOC-31, EMA, CAL, and MES was performed. Results: Among the suspected malignant effusion cases, 30 cases were AC and 12 cases were suspicious for malignancy by cytomorphology. MOC31 demonstrated 100% sensitivity (Sn) and 95.24% specificity (Sp), and EMA had 88.1% Sn and 92.86% Sp for AC cases. CAL demonstrated 100% and 97.62%, and MES 97.62% and 88.1% Sn and Sp in reactive mesothelial cells, respectively. Conclusion: In conclusion, combination of MOC-31 and CAL as a limited panel will be helpful in giving an appropriate diagnosis in difficult cases and thereby, help in patient management. In addition, ICC on cytospin smears gave results similar to cell blocks, and if standardised cytospin is simple technique to perform, unlike cell blocks. |
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issn | 0970-9371 |
language | English |
last_indexed | 2024-12-21T05:33:24Z |
publishDate | 2019-01-01 |
publisher | Wolters Kluwer Medknow Publications |
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spelling | doaj.art-07d7be9f677e46ddb15fb7436f67a6e82022-12-21T19:14:29ZengWolters Kluwer Medknow PublicationsJournal of Cytology0970-93712019-01-01361283110.4103/JOC.JOC_13_18Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinomaDevi SubbarayanJenna BhattacharyaPoonam RaniBembem KhuraijamShyama JainIntroduction: Although cytological examination helps in diagnosis of malignancy in serous effusion, at times it is difficult to differentiate atypical reactive mesothelial cells from adenocarcinoma (AC) cells. To resolve this problem, various ancillary methods have been used. Immunocytochemistry (ICC) is one such commonly used technique in which various panel of antibodies has been tried. Unfortunately, so far no unique marker is available to solve this issue. Hence, the present study evaluates the efficacy of four antibody panel comprising of MOC-31, epithelial membrane antigen (EMA), calretinin (CAL), and mesothelin (MES) to solve this problem. Materials and Methods: Forty-two cases suspected of malignant effusion in pleural/peritoneal fluid and 42 cases of reactive effusion were included. Cytospin smears were prepared and stained with Giemsa stain for cytomorphological diagnosis. Cytospin smears and cell blocks were made forICC. ICC for MOC-31, EMA, CAL, and MES was performed. Results: Among the suspected malignant effusion cases, 30 cases were AC and 12 cases were suspicious for malignancy by cytomorphology. MOC31 demonstrated 100% sensitivity (Sn) and 95.24% specificity (Sp), and EMA had 88.1% Sn and 92.86% Sp for AC cases. CAL demonstrated 100% and 97.62%, and MES 97.62% and 88.1% Sn and Sp in reactive mesothelial cells, respectively. Conclusion: In conclusion, combination of MOC-31 and CAL as a limited panel will be helpful in giving an appropriate diagnosis in difficult cases and thereby, help in patient management. In addition, ICC on cytospin smears gave results similar to cell blocks, and if standardised cytospin is simple technique to perform, unlike cell blocks.http://www.jcytol.org/article.asp?issn=0970-9371;year=2019;volume=36;issue=1;spage=28;epage=31;aulast=SubbarayanAdenocarcinomacalretinincell blockimmunocytochemistryMOC-31reactive mesothelial cells |
spellingShingle | Devi Subbarayan Jenna Bhattacharya Poonam Rani Bembem Khuraijam Shyama Jain Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma Journal of Cytology Adenocarcinoma calretinin cell block immunocytochemistry MOC-31 reactive mesothelial cells |
title | Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma |
title_full | Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma |
title_fullStr | Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma |
title_full_unstemmed | Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma |
title_short | Use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma |
title_sort | use of panel of markers in serous effusion to distinguish reactive mesothelial cells from adenocarcinoma |
topic | Adenocarcinoma calretinin cell block immunocytochemistry MOC-31 reactive mesothelial cells |
url | http://www.jcytol.org/article.asp?issn=0970-9371;year=2019;volume=36;issue=1;spage=28;epage=31;aulast=Subbarayan |
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