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Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis
OBJECTIVES: A rising frequency of colorectal carcinoma has been noted in recent years in Pakistan. In the present study, we aimed to evaluate clinicopathologic features of colorectal carcinoma in our population so that protocols could be developed to stratify patients that may require further biomar...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775533/ https://www.ncbi.nlm.nih.gov/pubmed/29351808 http://dx.doi.org/10.1186/s13104-018-3183-2 |
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author | Hashmi, Atif Ali Hashmi, Shumaila Kanwal Ali, Navaira Thara, Komal Ali, Rabia Edhi, Muhammad Muzzammil Faridi, Naveen Khan, Amir |
author_facet | Hashmi, Atif Ali Hashmi, Shumaila Kanwal Ali, Navaira Thara, Komal Ali, Rabia Edhi, Muhammad Muzzammil Faridi, Naveen Khan, Amir |
author_sort | Hashmi, Atif Ali |
collection | PubMed |
description | OBJECTIVES: A rising frequency of colorectal carcinoma has been noted in recent years in Pakistan. In the present study, we aimed to evaluate clinicopathologic features of colorectal carcinoma in our population so that protocols could be developed to stratify patients that may require further biomarker/molecular testing. Furthermore, histological features which predict higher T and N stage were also evaluated. RESULTS: Median age at diagnosis was 54.5 (19–85) years. 79% cases were of conventional adenocarcinoma while 13% cases were of mucinous carcinoma. Most of the cases were at T3 stage (81%), while 27 and 68% of cases revealed lymphovascular invasion and nodal metastasis respectively. Mucinous and signet ring tumors were associated with a higher N stage. Pre-existing polyp was associated with lower T and N stage. We found a high proportion of our cases to present at advanced T-stage. Tumor grade and lymphovascular invasion were found to be associated with higher N-stage while tumor infiltrating lymphocytes was associated with lower T and N-stage. Moreover, a high frequency of mucinous differentiation may be linked to microsatellite instability in our cases of colorectal carcinoma; therefore, we suggest that microsatellite instability testing in colorectal carcinoma should be evaluated in our setup. |
format | Online Article Text |
id | pubmed-5775533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57755332018-01-31 Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis Hashmi, Atif Ali Hashmi, Shumaila Kanwal Ali, Navaira Thara, Komal Ali, Rabia Edhi, Muhammad Muzzammil Faridi, Naveen Khan, Amir BMC Res Notes Research Note OBJECTIVES: A rising frequency of colorectal carcinoma has been noted in recent years in Pakistan. In the present study, we aimed to evaluate clinicopathologic features of colorectal carcinoma in our population so that protocols could be developed to stratify patients that may require further biomarker/molecular testing. Furthermore, histological features which predict higher T and N stage were also evaluated. RESULTS: Median age at diagnosis was 54.5 (19–85) years. 79% cases were of conventional adenocarcinoma while 13% cases were of mucinous carcinoma. Most of the cases were at T3 stage (81%), while 27 and 68% of cases revealed lymphovascular invasion and nodal metastasis respectively. Mucinous and signet ring tumors were associated with a higher N stage. Pre-existing polyp was associated with lower T and N stage. We found a high proportion of our cases to present at advanced T-stage. Tumor grade and lymphovascular invasion were found to be associated with higher N-stage while tumor infiltrating lymphocytes was associated with lower T and N-stage. Moreover, a high frequency of mucinous differentiation may be linked to microsatellite instability in our cases of colorectal carcinoma; therefore, we suggest that microsatellite instability testing in colorectal carcinoma should be evaluated in our setup. BioMed Central 2018-01-19 /pmc/articles/PMC5775533/ /pubmed/29351808 http://dx.doi.org/10.1186/s13104-018-3183-2 Text en © The Author(s) 2018 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Hashmi, Atif Ali Hashmi, Shumaila Kanwal Ali, Navaira Thara, Komal Ali, Rabia Edhi, Muhammad Muzzammil Faridi, Naveen Khan, Amir Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis |
title | Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis |
title_full | Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis |
title_fullStr | Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis |
title_full_unstemmed | Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis |
title_short | Clinicopathologic features of colorectal carcinoma: features predicting higher T-stage and nodal metastasis |
title_sort | clinicopathologic features of colorectal carcinoma: features predicting higher t-stage and nodal metastasis |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775533/ https://www.ncbi.nlm.nih.gov/pubmed/29351808 http://dx.doi.org/10.1186/s13104-018-3183-2 |
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