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Intraductal carcinoma of the prostate: a critical re-appraisal
Intraductal carcinoma of the prostate gland (IDCP), which is now categorised as a distinct entity by WHO 2016, includes two biologically distinct diseases. IDCP associated with invasive carcinoma (IDCP-inv) generally represents a growth pattern of invasive prostatic adenocarcinoma while the rarely e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505500/ https://www.ncbi.nlm.nih.gov/pubmed/30825003 http://dx.doi.org/10.1007/s00428-019-02544-6 |
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author | Varma, Murali Delahunt, Brett Egevad, Lars Samaratunga, Hemamali Kristiansen, Glen |
author_facet | Varma, Murali Delahunt, Brett Egevad, Lars Samaratunga, Hemamali Kristiansen, Glen |
author_sort | Varma, Murali |
collection | PubMed |
description | Intraductal carcinoma of the prostate gland (IDCP), which is now categorised as a distinct entity by WHO 2016, includes two biologically distinct diseases. IDCP associated with invasive carcinoma (IDCP-inv) generally represents a growth pattern of invasive prostatic adenocarcinoma while the rarely encountered pure IDCP is a precursor of prostate cancer. This review highlights issues that require further discussion and clarification. The diagnostic criterion “nuclear size at least 6 times normal” is ambiguous as “size” could refer to either nuclear area or diameter. If area, then this criterion could be re-defined as nuclear diameter at least three times normal as it is difficult to visually compare area of nuclei. It is also unclear whether IDCP could also include tumours with ductal morphology. There is no consensus whether pure IDCP in needle biopsies should be managed with re-biopsy or radical therapy. A pragmatic approach would be to recommend radical therapy only for extensive pure IDCP that is morphologically unequivocal for high-grade prostate cancer. Active surveillance is not appropriate when low-grade invasive cancer is associated with IDCP, as such patients usually have unsampled high-grade prostatic adenocarcinoma. It is generally recommended that IDCP component of IDCP-inv should be included in tumour extent but not grade. However, there are good arguments in favour of grading IDCP associated with invasive cancer. All historical as well as contemporary Gleason outcome data are based on morphology and would have included an associated IDCP component in the tumour grade. WHO 2016 recommends that IDCP should not be graded, but it is unclear whether this applies to both pure IDCP and IDCP-inv. |
format | Online Article Text |
id | pubmed-6505500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-65055002019-05-28 Intraductal carcinoma of the prostate: a critical re-appraisal Varma, Murali Delahunt, Brett Egevad, Lars Samaratunga, Hemamali Kristiansen, Glen Virchows Arch Review and Perspectives Intraductal carcinoma of the prostate gland (IDCP), which is now categorised as a distinct entity by WHO 2016, includes two biologically distinct diseases. IDCP associated with invasive carcinoma (IDCP-inv) generally represents a growth pattern of invasive prostatic adenocarcinoma while the rarely encountered pure IDCP is a precursor of prostate cancer. This review highlights issues that require further discussion and clarification. The diagnostic criterion “nuclear size at least 6 times normal” is ambiguous as “size” could refer to either nuclear area or diameter. If area, then this criterion could be re-defined as nuclear diameter at least three times normal as it is difficult to visually compare area of nuclei. It is also unclear whether IDCP could also include tumours with ductal morphology. There is no consensus whether pure IDCP in needle biopsies should be managed with re-biopsy or radical therapy. A pragmatic approach would be to recommend radical therapy only for extensive pure IDCP that is morphologically unequivocal for high-grade prostate cancer. Active surveillance is not appropriate when low-grade invasive cancer is associated with IDCP, as such patients usually have unsampled high-grade prostatic adenocarcinoma. It is generally recommended that IDCP component of IDCP-inv should be included in tumour extent but not grade. However, there are good arguments in favour of grading IDCP associated with invasive cancer. All historical as well as contemporary Gleason outcome data are based on morphology and would have included an associated IDCP component in the tumour grade. WHO 2016 recommends that IDCP should not be graded, but it is unclear whether this applies to both pure IDCP and IDCP-inv. Springer Berlin Heidelberg 2019-03-01 2019 /pmc/articles/PMC6505500/ /pubmed/30825003 http://dx.doi.org/10.1007/s00428-019-02544-6 Text en © The Author(s) 2019 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review and Perspectives Varma, Murali Delahunt, Brett Egevad, Lars Samaratunga, Hemamali Kristiansen, Glen Intraductal carcinoma of the prostate: a critical re-appraisal |
title | Intraductal carcinoma of the prostate: a critical re-appraisal |
title_full | Intraductal carcinoma of the prostate: a critical re-appraisal |
title_fullStr | Intraductal carcinoma of the prostate: a critical re-appraisal |
title_full_unstemmed | Intraductal carcinoma of the prostate: a critical re-appraisal |
title_short | Intraductal carcinoma of the prostate: a critical re-appraisal |
title_sort | intraductal carcinoma of the prostate: a critical re-appraisal |
topic | Review and Perspectives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505500/ https://www.ncbi.nlm.nih.gov/pubmed/30825003 http://dx.doi.org/10.1007/s00428-019-02544-6 |
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