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Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast

OBJECTIVE: To determine the frequency of the immunohistochemical profiles of a series of high-grade ductal carcinoma in situ of the breast. METHODS: One hundred and twenty-one cases of high-grade ductal carcinoma in situ, pure or associated with invasive mammary carcinoma, were identified from 2003...

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Autores principales: Perez, Amanda Arantes, Rocha, Rafael Malagoli, Balabram, Débora, da Silva Souza, Átila, Gobbi, Helenice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654337/
https://www.ncbi.nlm.nih.gov/pubmed/23778408
http://dx.doi.org/10.6061/clinics/2013(05)15
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author Perez, Amanda Arantes
Rocha, Rafael Malagoli
Balabram, Débora
da Silva Souza, Átila
Gobbi, Helenice
author_facet Perez, Amanda Arantes
Rocha, Rafael Malagoli
Balabram, Débora
da Silva Souza, Átila
Gobbi, Helenice
author_sort Perez, Amanda Arantes
collection PubMed
description OBJECTIVE: To determine the frequency of the immunohistochemical profiles of a series of high-grade ductal carcinoma in situ of the breast. METHODS: One hundred and twenty-one cases of high-grade ductal carcinoma in situ, pure or associated with invasive mammary carcinoma, were identified from 2003 to 2008 and examined with immunohistochemistry for estrogen receptor, human epidermal growth factor receptor 2, cytokeratin 5, and epidermal growth factor receptor. The tumors were placed into five subgroups: luminal A, luminal B, HER2, basal-like, and “not classified”. RESULTS: The frequencies of the immunophenotypes of pure ductal carcinoma in situ were the following: luminal A (24/42 cases; 57.1%), luminal B (05/42 cases; 11.9%), HER2 (07/42 cases; 16.7%), basal-like phenotype (00/42 cases; 0%), and “not classified” (06/42 cases; 14.3%). The immunophenotypes of ductal carcinoma in situ associated with invasive carcinoma were the following: luminal A (46/79 cases; 58.2%), luminal B (10/79 cases; 12.7%), HER2 (06/79 cases; 7.6%), basal-like (06/79 cases; 7.6%), and “not classified” (11/79 cases; 13.9%). There was no significant difference in the immunophenotype frequencies between pure ductal carcinoma in situ and ductal carcinoma in situ associated with invasive carcinoma (p>0.05). High agreement was observed in immunophenotypes between both components (kappa = 0.867). CONCLUSION: The most common immunophenotype of pure ductal carcinoma in situ was luminal A, followed by HER2. The basal-like phenotype was observed only in ductal carcinoma in situ associated with invasive carcinoma, which had a similar phenotype.
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spelling pubmed-36543372013-05-17 Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast Perez, Amanda Arantes Rocha, Rafael Malagoli Balabram, Débora da Silva Souza, Átila Gobbi, Helenice Clinics (Sao Paulo) Clinical Science OBJECTIVE: To determine the frequency of the immunohistochemical profiles of a series of high-grade ductal carcinoma in situ of the breast. METHODS: One hundred and twenty-one cases of high-grade ductal carcinoma in situ, pure or associated with invasive mammary carcinoma, were identified from 2003 to 2008 and examined with immunohistochemistry for estrogen receptor, human epidermal growth factor receptor 2, cytokeratin 5, and epidermal growth factor receptor. The tumors were placed into five subgroups: luminal A, luminal B, HER2, basal-like, and “not classified”. RESULTS: The frequencies of the immunophenotypes of pure ductal carcinoma in situ were the following: luminal A (24/42 cases; 57.1%), luminal B (05/42 cases; 11.9%), HER2 (07/42 cases; 16.7%), basal-like phenotype (00/42 cases; 0%), and “not classified” (06/42 cases; 14.3%). The immunophenotypes of ductal carcinoma in situ associated with invasive carcinoma were the following: luminal A (46/79 cases; 58.2%), luminal B (10/79 cases; 12.7%), HER2 (06/79 cases; 7.6%), basal-like (06/79 cases; 7.6%), and “not classified” (11/79 cases; 13.9%). There was no significant difference in the immunophenotype frequencies between pure ductal carcinoma in situ and ductal carcinoma in situ associated with invasive carcinoma (p>0.05). High agreement was observed in immunophenotypes between both components (kappa = 0.867). CONCLUSION: The most common immunophenotype of pure ductal carcinoma in situ was luminal A, followed by HER2. The basal-like phenotype was observed only in ductal carcinoma in situ associated with invasive carcinoma, which had a similar phenotype. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013-05 /pmc/articles/PMC3654337/ /pubmed/23778408 http://dx.doi.org/10.6061/clinics/2013(05)15 Text en Copyright © 2013 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Perez, Amanda Arantes
Rocha, Rafael Malagoli
Balabram, Débora
da Silva Souza, Átila
Gobbi, Helenice
Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
title Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
title_full Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
title_fullStr Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
title_full_unstemmed Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
title_short Immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
title_sort immunohistochemical profile of high-grade ductal carcinoma in situ of the breast
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654337/
https://www.ncbi.nlm.nih.gov/pubmed/23778408
http://dx.doi.org/10.6061/clinics/2013(05)15
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