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Colorectal cancer in young adults: a retrospective study of 32 tunisian patients

Young people under the age of 40 with colorectal cancer represent a distinct subgroup with a more aggressive disease behaviour compared to older patients. This study aim to provide an updated overview on clinicopathological features, treatment and outcome of colorectal cancer in young adults under t...

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Autores principales: Limaiem, Faten, Azzabi, Sonia, Sassi, Asma, Mzabi, Sabeh, Bouraoui, Saadia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457724/
https://www.ncbi.nlm.nih.gov/pubmed/31007809
http://dx.doi.org/10.11604/pamj.2018.31.62.11043
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author Limaiem, Faten
Azzabi, Sonia
Sassi, Asma
Mzabi, Sabeh
Bouraoui, Saadia
author_facet Limaiem, Faten
Azzabi, Sonia
Sassi, Asma
Mzabi, Sabeh
Bouraoui, Saadia
author_sort Limaiem, Faten
collection PubMed
description Young people under the age of 40 with colorectal cancer represent a distinct subgroup with a more aggressive disease behaviour compared to older patients. This study aim to provide an updated overview on clinicopathological features, treatment and outcome of colorectal cancer in young adults under the age of 40. In our retrospective study, we reviewed 32 cases of colorectal cancer in young adults aged less than 40 years that were diagnosed at the pathology department of Mongi Slim hospital over a fifteen-year period (April 2000 - November 2014). Our study group included 13 male and 19 female patients (sex-ratio M/F = 0,68) between 17 and 39 years of age (mean = 31,25 years). The presenting clinical symptoms were dominated by altered bowel habits (n=17), followed by bleeding per rectum (n=16). Histopathological examination of the surgical and biopsy specimens established the diagnosis of mucinous adenocarcinoma in nine cases, well-differentiated adenocarcinoma in 11 cases, moderately differentiated adenocarcinoma in six cases, poorly differentiated adenocarcinoma in four cases and signet ring cell carcinoma in two cases. The tumours were classified after surgery as stage I (n = 2) (6%), stage IIA (n = 7) (22%), stage IIB (n=4) (13%), stage IIC (n=1) (3%), stage IIIB (n=8) (25%), stage IIIC (n= 4) (12%), stage IVA (n=4) (13%) and stage IVB (n=2) (6%). During the follow-up period which ranged between one month and 9 years, local recurrence of the tumour occurred in six cases, seven patients had hepatic metastases and seven patients died after a mean follow-up period of seven months. Molecular genetic studies are increasing the understanding of the pathobiology of colorectal cancer and may ultimately allow at-risk patients to be identified at an earlier stage.
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spelling pubmed-64577242019-04-19 Colorectal cancer in young adults: a retrospective study of 32 tunisian patients Limaiem, Faten Azzabi, Sonia Sassi, Asma Mzabi, Sabeh Bouraoui, Saadia Pan Afr Med J Case Series Young people under the age of 40 with colorectal cancer represent a distinct subgroup with a more aggressive disease behaviour compared to older patients. This study aim to provide an updated overview on clinicopathological features, treatment and outcome of colorectal cancer in young adults under the age of 40. In our retrospective study, we reviewed 32 cases of colorectal cancer in young adults aged less than 40 years that were diagnosed at the pathology department of Mongi Slim hospital over a fifteen-year period (April 2000 - November 2014). Our study group included 13 male and 19 female patients (sex-ratio M/F = 0,68) between 17 and 39 years of age (mean = 31,25 years). The presenting clinical symptoms were dominated by altered bowel habits (n=17), followed by bleeding per rectum (n=16). Histopathological examination of the surgical and biopsy specimens established the diagnosis of mucinous adenocarcinoma in nine cases, well-differentiated adenocarcinoma in 11 cases, moderately differentiated adenocarcinoma in six cases, poorly differentiated adenocarcinoma in four cases and signet ring cell carcinoma in two cases. The tumours were classified after surgery as stage I (n = 2) (6%), stage IIA (n = 7) (22%), stage IIB (n=4) (13%), stage IIC (n=1) (3%), stage IIIB (n=8) (25%), stage IIIC (n= 4) (12%), stage IVA (n=4) (13%) and stage IVB (n=2) (6%). During the follow-up period which ranged between one month and 9 years, local recurrence of the tumour occurred in six cases, seven patients had hepatic metastases and seven patients died after a mean follow-up period of seven months. Molecular genetic studies are increasing the understanding of the pathobiology of colorectal cancer and may ultimately allow at-risk patients to be identified at an earlier stage. The African Field Epidemiology Network 2018-09-27 /pmc/articles/PMC6457724/ /pubmed/31007809 http://dx.doi.org/10.11604/pamj.2018.31.62.11043 Text en © Colorectal cancer et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Series
Limaiem, Faten
Azzabi, Sonia
Sassi, Asma
Mzabi, Sabeh
Bouraoui, Saadia
Colorectal cancer in young adults: a retrospective study of 32 tunisian patients
title Colorectal cancer in young adults: a retrospective study of 32 tunisian patients
title_full Colorectal cancer in young adults: a retrospective study of 32 tunisian patients
title_fullStr Colorectal cancer in young adults: a retrospective study of 32 tunisian patients
title_full_unstemmed Colorectal cancer in young adults: a retrospective study of 32 tunisian patients
title_short Colorectal cancer in young adults: a retrospective study of 32 tunisian patients
title_sort colorectal cancer in young adults: a retrospective study of 32 tunisian patients
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457724/
https://www.ncbi.nlm.nih.gov/pubmed/31007809
http://dx.doi.org/10.11604/pamj.2018.31.62.11043
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