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The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives
A proportion of breast carcinomas develop as a result of a genetic predispostion to the disease. Prior to cloning of the BRCA1 and BRCA2 genes a limited number of studies were carried out to identify specific histopathological characteristics of hereditary breast cancer. These studies are the subjec...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
1999
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138507/ https://www.ncbi.nlm.nih.gov/pubmed/11250679 http://dx.doi.org/10.1186/bcr9 |
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author | van de Vijver, Marc J |
author_facet | van de Vijver, Marc J |
author_sort | van de Vijver, Marc J |
collection | PubMed |
description | A proportion of breast carcinomas develop as a result of a genetic predispostion to the disease. Prior to cloning of the BRCA1 and BRCA2 genes a limited number of studies were carried out to identify specific histopathological characteristics of hereditary breast cancer. These studies are the subject of this review. The main finding was the association of the (atypical) medullary type of breast cancer with a family history; the most important caveat being that medullary breast cancer is found more frequently in young patients. In view of the frequent bilateral occurrence of lobular cancer, this histologic type is also likely to be associated with a predisposing genetic defect. Future investigations will have to test this hypothesis. In addition to mutations in the BRCA1 and BRCA2 genes, there are as yet unidentified genetic defects predisposing to breast cancer development, and histopathology may well help in identifying these genes in the future. |
format | Text |
id | pubmed-138507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1385072003-02-27 The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives van de Vijver, Marc J Breast Cancer Res Review A proportion of breast carcinomas develop as a result of a genetic predispostion to the disease. Prior to cloning of the BRCA1 and BRCA2 genes a limited number of studies were carried out to identify specific histopathological characteristics of hereditary breast cancer. These studies are the subject of this review. The main finding was the association of the (atypical) medullary type of breast cancer with a family history; the most important caveat being that medullary breast cancer is found more frequently in young patients. In view of the frequent bilateral occurrence of lobular cancer, this histologic type is also likely to be associated with a predisposing genetic defect. Future investigations will have to test this hypothesis. In addition to mutations in the BRCA1 and BRCA2 genes, there are as yet unidentified genetic defects predisposing to breast cancer development, and histopathology may well help in identifying these genes in the future. BioMed Central 1999 1999-10-27 /pmc/articles/PMC138507/ /pubmed/11250679 http://dx.doi.org/10.1186/bcr9 Text en Copyright © 1999 Current Science Ltd |
spellingShingle | Review van de Vijver, Marc J The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives |
title | The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives |
title_full | The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives |
title_fullStr | The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives |
title_full_unstemmed | The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives |
title_short | The pathology of familial breast cancer: The pre-BRCA1/BRCA2 era - historical perspectives |
title_sort | pathology of familial breast cancer: the pre-brca1/brca2 era - historical perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138507/ https://www.ncbi.nlm.nih.gov/pubmed/11250679 http://dx.doi.org/10.1186/bcr9 |
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