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Histopathological and clonal study of combined lobular and ductal carcinoma of the breast
Lobular carcinoma in situ (LCIS) clinically constitutes a risk factor for the subsequent development of either invasive lobular carcinoma (ILC) or invasive ductal carcinoma (IDC). In order to approach the possibility of this common precursor of both ILC and IDC, we investigated combined lobular and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798103/ https://www.ncbi.nlm.nih.gov/pubmed/23782331 http://dx.doi.org/10.1111/pin.12065 |
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author | Tazaki, Eri Shishido-Hara, Yukiko Mizutani, Natsuko Nomura, Sachiyo Isaka, Hirotsugu Ito, Hiroki Imi, Kentaro Imoto, Shigeru Kamma, Hiroshi |
author_facet | Tazaki, Eri Shishido-Hara, Yukiko Mizutani, Natsuko Nomura, Sachiyo Isaka, Hirotsugu Ito, Hiroki Imi, Kentaro Imoto, Shigeru Kamma, Hiroshi |
author_sort | Tazaki, Eri |
collection | PubMed |
description | Lobular carcinoma in situ (LCIS) clinically constitutes a risk factor for the subsequent development of either invasive lobular carcinoma (ILC) or invasive ductal carcinoma (IDC). In order to approach the possibility of this common precursor of both ILC and IDC, we investigated combined lobular and ductal carcinomas. Thirty-two cases of lobular carcinoma were picked up out of 773 cases of operated breast carcinomas. The histopathological detailed re-examination using immunostain of E-cadherin and β-catenin revealed a rather high frequency of combined lobular carcinomas than previous reports. Clinicopathologically, combined lobular carcinomas were younger and smaller than pure lobular carcinomas, and the cytological atypia was relatively low. These results suggested that combined lobular carcinomas could be detected in the earlier stage of breast cancer. Furthermore, the lobular and ductal components of combined carcinomas coexisted in the neighborhood and were distributed contiguously. The immunohistochemical phenotypes of both components were accorded in most combined cases. A genetic analysis using methylation-specific PCR on the HUMARA gene demonstrated that the same allele was inactivated in both lobular and ductal components in all detectable cases of combined carcinoma. Therefore, it is reasonable to assume that both lobular and ductal components of combined carcinomas are clonal and derived from the LCIS as the common precursor lesion, which may contradict the conventional concept that the lobular and ductal carcinomas arise from distinct differentiation pathways. |
format | Online Article Text |
id | pubmed-3798103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37981032013-10-22 Histopathological and clonal study of combined lobular and ductal carcinoma of the breast Tazaki, Eri Shishido-Hara, Yukiko Mizutani, Natsuko Nomura, Sachiyo Isaka, Hirotsugu Ito, Hiroki Imi, Kentaro Imoto, Shigeru Kamma, Hiroshi Pathol Int Original Articles Lobular carcinoma in situ (LCIS) clinically constitutes a risk factor for the subsequent development of either invasive lobular carcinoma (ILC) or invasive ductal carcinoma (IDC). In order to approach the possibility of this common precursor of both ILC and IDC, we investigated combined lobular and ductal carcinomas. Thirty-two cases of lobular carcinoma were picked up out of 773 cases of operated breast carcinomas. The histopathological detailed re-examination using immunostain of E-cadherin and β-catenin revealed a rather high frequency of combined lobular carcinomas than previous reports. Clinicopathologically, combined lobular carcinomas were younger and smaller than pure lobular carcinomas, and the cytological atypia was relatively low. These results suggested that combined lobular carcinomas could be detected in the earlier stage of breast cancer. Furthermore, the lobular and ductal components of combined carcinomas coexisted in the neighborhood and were distributed contiguously. The immunohistochemical phenotypes of both components were accorded in most combined cases. A genetic analysis using methylation-specific PCR on the HUMARA gene demonstrated that the same allele was inactivated in both lobular and ductal components in all detectable cases of combined carcinoma. Therefore, it is reasonable to assume that both lobular and ductal components of combined carcinomas are clonal and derived from the LCIS as the common precursor lesion, which may contradict the conventional concept that the lobular and ductal carcinomas arise from distinct differentiation pathways. Blackwell Publishing Ltd 2013-06 2013-06-20 /pmc/articles/PMC3798103/ /pubmed/23782331 http://dx.doi.org/10.1111/pin.12065 Text en © 2013 Japanese Society of Pathology and Wiley Publishing Asia Pty Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Tazaki, Eri Shishido-Hara, Yukiko Mizutani, Natsuko Nomura, Sachiyo Isaka, Hirotsugu Ito, Hiroki Imi, Kentaro Imoto, Shigeru Kamma, Hiroshi Histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
title | Histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
title_full | Histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
title_fullStr | Histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
title_full_unstemmed | Histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
title_short | Histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
title_sort | histopathological and clonal study of combined lobular and ductal carcinoma of the breast |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798103/ https://www.ncbi.nlm.nih.gov/pubmed/23782331 http://dx.doi.org/10.1111/pin.12065 |
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