Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols

Detalhes bibliográficos
Autor(a) principal: Santos, Bruna
Data de Publicação: 2022
Outros Autores: Roque, Ruben, Pereira, Teresa, Mendonça, Paula, André, Saudade
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25758/set.488
Resumo: Background – Long-term preservation of fine-needle aspiration cytology slides is an essential requirement in cytopathology laboratories for the eventual performance of immunocytochemistry. ICQ contributes to a correct and complete diagnosis, considering that long-term morphological and antigenic preservation is essential to obtain reliable results. In this study, we intend to evaluate and compare the immunoexpression of TTF1, p40, and chromogranin A antigens in lung samples taken from the archive and stained with: i) Papanicolaou (Pap); ii) May-Grünwald Giemsa (MGG); iii) preserved in polyethylene glycol (PEG); and iv) processed as cell-block. Methods – Twenty-four fine needle aspiration cytology samples diagnosed as primary lung carcinoma with a sample processed by each of the protocols studied (Pap, MGG, PEG, and CB) were selected from the archive. Based on the diagnosis, immunostaining was performed with primary antibodies anti-TTF1 (adenocarcinomas), anti-p40 (squamous cell carcinomas), and anti-chromogranin A (neuroendocrine carcinomas). The quality of immunostaining was evaluated by two independent observers using an evaluation grid (rated from 0 to 27 points) that comprises parameters as: morphological preservation, specific staining intensity, sensitivity, specificity, and contrast. Results – The mean values obtained for CB, PEG, Pap, and MGG protocols were 21.58 (±4.54), 11.79 (±1.88), 22.25 (±5.30), 26.31 (±1.21) points respectively. CB achieved better results when compared to other protocols under study (p<0.05). When compared in pairs (Tuckey post-hoc) the only protocols that did not show statistically significant differences were Pap and PEG (p=0.0814). Conclusions – Cell-block is the elected protocol to perform ICQ for the samples and antigens under study. The Pap and PEG protocols showed loss of immunostaining, which could lead to false-negative results. Immunostaining was not observed in any sample with MGG protocol.
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spelling Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocolsImunocitoquímica em citologia aspirativa do pulmão: comparação de quatro protocolosImunocitoquímicaMay-Grϋnwald GiemsaPolietilenoglicolPapanicolaouProcessamentoImmunocytochemistryMay-Grϋnwald GiemsaPolyethyleneglycolPapanicolaouSample processingBackground – Long-term preservation of fine-needle aspiration cytology slides is an essential requirement in cytopathology laboratories for the eventual performance of immunocytochemistry. ICQ contributes to a correct and complete diagnosis, considering that long-term morphological and antigenic preservation is essential to obtain reliable results. In this study, we intend to evaluate and compare the immunoexpression of TTF1, p40, and chromogranin A antigens in lung samples taken from the archive and stained with: i) Papanicolaou (Pap); ii) May-Grünwald Giemsa (MGG); iii) preserved in polyethylene glycol (PEG); and iv) processed as cell-block. Methods – Twenty-four fine needle aspiration cytology samples diagnosed as primary lung carcinoma with a sample processed by each of the protocols studied (Pap, MGG, PEG, and CB) were selected from the archive. Based on the diagnosis, immunostaining was performed with primary antibodies anti-TTF1 (adenocarcinomas), anti-p40 (squamous cell carcinomas), and anti-chromogranin A (neuroendocrine carcinomas). The quality of immunostaining was evaluated by two independent observers using an evaluation grid (rated from 0 to 27 points) that comprises parameters as: morphological preservation, specific staining intensity, sensitivity, specificity, and contrast. Results – The mean values obtained for CB, PEG, Pap, and MGG protocols were 21.58 (±4.54), 11.79 (±1.88), 22.25 (±5.30), 26.31 (±1.21) points respectively. CB achieved better results when compared to other protocols under study (p<0.05). When compared in pairs (Tuckey post-hoc) the only protocols that did not show statistically significant differences were Pap and PEG (p=0.0814). Conclusions – Cell-block is the elected protocol to perform ICQ for the samples and antigens under study. The Pap and PEG protocols showed loss of immunostaining, which could lead to false-negative results. Immunostaining was not observed in any sample with MGG protocol.Introdução – A preservação a longo prazo de lâminas de citologia aspirativa por agulha fina (CAAF) é um requisito essencial nos laboratórios de citopatologia para a posterior realização de imunocitoquímica (ICQ). A ICQ contribui para um diagnóstico correto e completo, sendo essencial a preservação morfológica e antigénica a longo prazo para obter resultados confiáveis. Neste estudo pretende-se avaliar a imunoexpressão dos antigénios TTF1, p40 e cromogranina A em amostras de CAAF do pulmão retiradas do arquivo e coradas pelos métodos de: i) Papanicolaou (Pap) e ii) May-Grünwald Giemsa (MGG); iii) preservadas em polietilenoglicol (PEG); e iv) processadas como citobloco (CB). Métodos – Foram selecionados do arquivo 24 exames de CAAF com diagnóstico de carcinoma primário do pulmão, com amostra processada por cada um dos protocolos em estudo (Pap, MGG, PEG e CB). Com base no diagnóstico foi realizada imunomarcação com anticorpos primários antí-TTF1 (adenocarcinomas), antí-p40 (carcinomas pavimentocelulares) e anti-cromogranina A (carcinomas neuroendócrinos). A qualidade da imunomarcação foi aferida por dois avaliadores independentes com recurso a uma escala, com classificação entre 0 e 27 pontos, e que compreende os parâmetros: preservação morfológica, intensidade da marcação específica, sensibilidade, especificidade e contraste. Resultados – A pontuação média obtida para os métodos Pap, MGG, PEG e CB foi de 21,58 (±4,54), 11,79 (±1,88), 22,25 (±5,30), 26,31 (±1,21) pontos, respetivamente. O CB conseguiu resultados superiores aos restantes protocolos em estudo (p<0,05). Quando comparados os protocolos a par (post-hoc de Tuckey), os únicos que não apresentaram diferenças estatisticamente significativas entre si foram Pap e PEG (p=0,814). Conclusões – O CB é o protocolo de eleição para a realização de ICQ nas amostras e para os antigénios em estudo. Os métodos Pap e PEG apresentaram perda de imunormarcação, podendo levar a resultados falso-negativos. O protocolo de MGG não obteve imunomarcação em nenhuma amostra.Escola Superior de Tecnologia da Saúde de Lisboa (Instituto Politécnico de Lisboa)2022-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.25758/set.488oai:journals.ipl.pt:article/488Saúde e Tecnologia; No. 26 (2022): Maio 2022; 27-35Saúde & Tecnologia; N.º 26 (2022): Maio 2022; 27-351646-9704reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://journals.ipl.pt/stecnologia/article/view/488https://doi.org/10.25758/set.488https://journals.ipl.pt/stecnologia/article/view/488/577Santos, BrunaRoque, RubenPereira, TeresaMendonça, PaulaAndré, Saudadeinfo:eu-repo/semantics/openAccess2022-12-20T10:58:36Zoai:journals.ipl.pt:article/488Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:21:20.189519Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
Imunocitoquímica em citologia aspirativa do pulmão: comparação de quatro protocolos
title Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
spellingShingle Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
Santos, Bruna
Imunocitoquímica
May-Grϋnwald Giemsa
Polietilenoglicol
Papanicolaou
Processamento
Immunocytochemistry
May-Grϋnwald Giemsa
Polyethyleneglycol
Papanicolaou
Sample processing
title_short Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
title_full Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
title_fullStr Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
title_full_unstemmed Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
title_sort Immunocytochemistry in lung fine needle aspiration cytology: comparison of four protocols
author Santos, Bruna
author_facet Santos, Bruna
Roque, Ruben
Pereira, Teresa
Mendonça, Paula
André, Saudade
author_role author
author2 Roque, Ruben
Pereira, Teresa
Mendonça, Paula
André, Saudade
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Santos, Bruna
Roque, Ruben
Pereira, Teresa
Mendonça, Paula
André, Saudade
dc.subject.por.fl_str_mv Imunocitoquímica
May-Grϋnwald Giemsa
Polietilenoglicol
Papanicolaou
Processamento
Immunocytochemistry
May-Grϋnwald Giemsa
Polyethyleneglycol
Papanicolaou
Sample processing
topic Imunocitoquímica
May-Grϋnwald Giemsa
Polietilenoglicol
Papanicolaou
Processamento
Immunocytochemistry
May-Grϋnwald Giemsa
Polyethyleneglycol
Papanicolaou
Sample processing
description Background – Long-term preservation of fine-needle aspiration cytology slides is an essential requirement in cytopathology laboratories for the eventual performance of immunocytochemistry. ICQ contributes to a correct and complete diagnosis, considering that long-term morphological and antigenic preservation is essential to obtain reliable results. In this study, we intend to evaluate and compare the immunoexpression of TTF1, p40, and chromogranin A antigens in lung samples taken from the archive and stained with: i) Papanicolaou (Pap); ii) May-Grünwald Giemsa (MGG); iii) preserved in polyethylene glycol (PEG); and iv) processed as cell-block. Methods – Twenty-four fine needle aspiration cytology samples diagnosed as primary lung carcinoma with a sample processed by each of the protocols studied (Pap, MGG, PEG, and CB) were selected from the archive. Based on the diagnosis, immunostaining was performed with primary antibodies anti-TTF1 (adenocarcinomas), anti-p40 (squamous cell carcinomas), and anti-chromogranin A (neuroendocrine carcinomas). The quality of immunostaining was evaluated by two independent observers using an evaluation grid (rated from 0 to 27 points) that comprises parameters as: morphological preservation, specific staining intensity, sensitivity, specificity, and contrast. Results – The mean values obtained for CB, PEG, Pap, and MGG protocols were 21.58 (±4.54), 11.79 (±1.88), 22.25 (±5.30), 26.31 (±1.21) points respectively. CB achieved better results when compared to other protocols under study (p<0.05). When compared in pairs (Tuckey post-hoc) the only protocols that did not show statistically significant differences were Pap and PEG (p=0.0814). Conclusions – Cell-block is the elected protocol to perform ICQ for the samples and antigens under study. The Pap and PEG protocols showed loss of immunostaining, which could lead to false-negative results. Immunostaining was not observed in any sample with MGG protocol.
publishDate 2022
dc.date.none.fl_str_mv 2022-06-01
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dc.identifier.uri.fl_str_mv https://doi.org/10.25758/set.488
oai:journals.ipl.pt:article/488
url https://doi.org/10.25758/set.488
identifier_str_mv oai:journals.ipl.pt:article/488
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dc.relation.none.fl_str_mv https://journals.ipl.pt/stecnologia/article/view/488
https://doi.org/10.25758/set.488
https://journals.ipl.pt/stecnologia/article/view/488/577
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Escola Superior de Tecnologia da Saúde de Lisboa (Instituto Politécnico de Lisboa)
publisher.none.fl_str_mv Escola Superior de Tecnologia da Saúde de Lisboa (Instituto Politécnico de Lisboa)
dc.source.none.fl_str_mv Saúde e Tecnologia; No. 26 (2022): Maio 2022; 27-35
Saúde & Tecnologia; N.º 26 (2022): Maio 2022; 27-35
1646-9704
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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