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Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients

BACKGROUND: The surveillance of subjects at risk of pancreatic cancer is restricted to clinical research; the incidence of familial pancreatic cancer needs to be better established. Thus, we aimed to evaluate the frequency of familial pancreatic cancer in a population of hospitalized patients with p...

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Autores principales: Mughetti, Martina, Calculli, Lucia, Chiesa, Anna Maria, Ciccarese, Federica, Rrusho, Odeta, Pezzilli, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714470/
https://www.ncbi.nlm.nih.gov/pubmed/26767414
http://dx.doi.org/10.1186/s12876-016-0421-8
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author Mughetti, Martina
Calculli, Lucia
Chiesa, Anna Maria
Ciccarese, Federica
Rrusho, Odeta
Pezzilli, Raffaele
author_facet Mughetti, Martina
Calculli, Lucia
Chiesa, Anna Maria
Ciccarese, Federica
Rrusho, Odeta
Pezzilli, Raffaele
author_sort Mughetti, Martina
collection PubMed
description BACKGROUND: The surveillance of subjects at risk of pancreatic cancer is restricted to clinical research; the incidence of familial pancreatic cancer needs to be better established. Thus, we aimed to evaluate the frequency of familial pancreatic cancer in a population of hospitalized patients with pancreatic cancer. METHODS: A retrospective study based on the hospital charts of patients discharged with a diagnosis of pancreatic cancer. One hundred and eighty-seven patients or their relatives were called for a phone interview. RESULTS: There were 97 males (51.9 %) and 90 (48.1 %) females. The overall mean ± SD age was 67.3 ± 11.8 years; the age of males was similar to that of females (P = 0140). The mean size of the tumors found was 36.3 ± 17.4 mm (range of 5–110 mm); it was related to gender but was not related to the site of the tumor or the age of the patient. Regarding genetic diseases, three females (1.6 %) had familial adenomatous polyposis; three patients (1 male and two females) (1.6 %) had at least one relative with pancreatic cancer whereas only one 80-year old male patient (0.5 %) had two relatives affected by pancreatic cancer (the mother had died at the 65 years of age and the brother had died at 75 years of age). CONCLUSIONS: The frequency of familial pancreatic ductal adenocarcinoma is small, but its importance, from the point of view of early diagnosis, is not negligible and patients with a risk of familial cancer merit an appropriate clinical follow-up.
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spelling pubmed-47144702016-01-16 Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients Mughetti, Martina Calculli, Lucia Chiesa, Anna Maria Ciccarese, Federica Rrusho, Odeta Pezzilli, Raffaele BMC Gastroenterol Research Article BACKGROUND: The surveillance of subjects at risk of pancreatic cancer is restricted to clinical research; the incidence of familial pancreatic cancer needs to be better established. Thus, we aimed to evaluate the frequency of familial pancreatic cancer in a population of hospitalized patients with pancreatic cancer. METHODS: A retrospective study based on the hospital charts of patients discharged with a diagnosis of pancreatic cancer. One hundred and eighty-seven patients or their relatives were called for a phone interview. RESULTS: There were 97 males (51.9 %) and 90 (48.1 %) females. The overall mean ± SD age was 67.3 ± 11.8 years; the age of males was similar to that of females (P = 0140). The mean size of the tumors found was 36.3 ± 17.4 mm (range of 5–110 mm); it was related to gender but was not related to the site of the tumor or the age of the patient. Regarding genetic diseases, three females (1.6 %) had familial adenomatous polyposis; three patients (1 male and two females) (1.6 %) had at least one relative with pancreatic cancer whereas only one 80-year old male patient (0.5 %) had two relatives affected by pancreatic cancer (the mother had died at the 65 years of age and the brother had died at 75 years of age). CONCLUSIONS: The frequency of familial pancreatic ductal adenocarcinoma is small, but its importance, from the point of view of early diagnosis, is not negligible and patients with a risk of familial cancer merit an appropriate clinical follow-up. BioMed Central 2016-01-15 /pmc/articles/PMC4714470/ /pubmed/26767414 http://dx.doi.org/10.1186/s12876-016-0421-8 Text en © Mughetti et al. 2016 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 Article
Mughetti, Martina
Calculli, Lucia
Chiesa, Anna Maria
Ciccarese, Federica
Rrusho, Odeta
Pezzilli, Raffaele
Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
title Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
title_full Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
title_fullStr Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
title_full_unstemmed Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
title_short Implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
title_sort implications and issues related to familial pancreatic cancer: a cohort study of hospitalized patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714470/
https://www.ncbi.nlm.nih.gov/pubmed/26767414
http://dx.doi.org/10.1186/s12876-016-0421-8
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