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Precursor lesions of early onset pancreatic cancer

Early onset pancreatic cancer (EOPC) constitutes less than 5% of all newly diagnosed cases of pancreatic cancer (PC). Although histopathological characteristics of EOPC have been described, no detailed reports on precursor lesions of EOPC are available. In the present study, we aimed to describe his...

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Autores principales: Liszka, Łukasz, Pająk, Jacek, Mrowiec, Sławomir, Zielińska-Pająk, Ewa, Gołka, Dariusz, Lampe, Paweł
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062030/
https://www.ncbi.nlm.nih.gov/pubmed/21369801
http://dx.doi.org/10.1007/s00428-011-1056-3
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author Liszka, Łukasz
Pająk, Jacek
Mrowiec, Sławomir
Zielińska-Pająk, Ewa
Gołka, Dariusz
Lampe, Paweł
author_facet Liszka, Łukasz
Pająk, Jacek
Mrowiec, Sławomir
Zielińska-Pająk, Ewa
Gołka, Dariusz
Lampe, Paweł
author_sort Liszka, Łukasz
collection PubMed
description Early onset pancreatic cancer (EOPC) constitutes less than 5% of all newly diagnosed cases of pancreatic cancer (PC). Although histopathological characteristics of EOPC have been described, no detailed reports on precursor lesions of EOPC are available. In the present study, we aimed to describe histopathological picture of extratumoral parenchyma in 23 cases of EOPCs (definition based on the threshold value of 45 years of age) with particular emphasis on two types of precursor lesions of PC: pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMNs). The types, grades, and densities of precursor lesions of PC were compared in patients with EOPCs, in young patients with neuroendocrine neoplasms (NENs), and in older (at the age of 46 or more) patients with PC. PanINs were found in 95.6% of cases of EOPCs. PanINs-3 were found in 39.1% of EOPC cases. Densities of all PanIN grades in EOPC cases were larger than in young patients with NENs. Density of PanINs-1A in EOPC cases was larger than in older patients with PC, but densities of PanINs of other grades were comparable. IPMN was found only in a single patient with EOPC but in 20% of older patients with PC. PanINs are the most prevalent precursor lesions of EOPC. IPMNs are rarely precursor lesions of EOPC. Relatively high density of low-grade PanINs-1 in extratumoral parenchyma of patients with EOPC may result from unknown multifocal genetic alterations in pancreatic tissue in patients with EOPCs.
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spelling pubmed-30620302011-04-05 Precursor lesions of early onset pancreatic cancer Liszka, Łukasz Pająk, Jacek Mrowiec, Sławomir Zielińska-Pająk, Ewa Gołka, Dariusz Lampe, Paweł Virchows Arch Original Article Early onset pancreatic cancer (EOPC) constitutes less than 5% of all newly diagnosed cases of pancreatic cancer (PC). Although histopathological characteristics of EOPC have been described, no detailed reports on precursor lesions of EOPC are available. In the present study, we aimed to describe histopathological picture of extratumoral parenchyma in 23 cases of EOPCs (definition based on the threshold value of 45 years of age) with particular emphasis on two types of precursor lesions of PC: pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMNs). The types, grades, and densities of precursor lesions of PC were compared in patients with EOPCs, in young patients with neuroendocrine neoplasms (NENs), and in older (at the age of 46 or more) patients with PC. PanINs were found in 95.6% of cases of EOPCs. PanINs-3 were found in 39.1% of EOPC cases. Densities of all PanIN grades in EOPC cases were larger than in young patients with NENs. Density of PanINs-1A in EOPC cases was larger than in older patients with PC, but densities of PanINs of other grades were comparable. IPMN was found only in a single patient with EOPC but in 20% of older patients with PC. PanINs are the most prevalent precursor lesions of EOPC. IPMNs are rarely precursor lesions of EOPC. Relatively high density of low-grade PanINs-1 in extratumoral parenchyma of patients with EOPC may result from unknown multifocal genetic alterations in pancreatic tissue in patients with EOPCs. Springer-Verlag 2011-03-03 2011 /pmc/articles/PMC3062030/ /pubmed/21369801 http://dx.doi.org/10.1007/s00428-011-1056-3 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Liszka, Łukasz
Pająk, Jacek
Mrowiec, Sławomir
Zielińska-Pająk, Ewa
Gołka, Dariusz
Lampe, Paweł
Precursor lesions of early onset pancreatic cancer
title Precursor lesions of early onset pancreatic cancer
title_full Precursor lesions of early onset pancreatic cancer
title_fullStr Precursor lesions of early onset pancreatic cancer
title_full_unstemmed Precursor lesions of early onset pancreatic cancer
title_short Precursor lesions of early onset pancreatic cancer
title_sort precursor lesions of early onset pancreatic cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062030/
https://www.ncbi.nlm.nih.gov/pubmed/21369801
http://dx.doi.org/10.1007/s00428-011-1056-3
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