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Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study

BACKGROUND AND AIM: Pancreatic ductal adenocarcinoma (PDAC) is a lethal cancer, partly because its early detection is difficult. This study aimed to identify computed tomography (CT) findings associated with PDAC prior to diagnosis. METHODS: Past CT images were retrospectively collected from the PDA...

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Autores principales: Koiwai, Akinobu, Hirota, Morihisa, Matsuura, Tomonori, Itoh, Takehito, Kin, Ryo, Katayama, Tomofumi, Endo, Katsuya, Takasu, Atsuko, Kogure, Takayuki, Murakami, Kazuhiro, Satoh, Kennichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290266/
https://www.ncbi.nlm.nih.gov/pubmed/37359111
http://dx.doi.org/10.1002/jgh3.12930
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author Koiwai, Akinobu
Hirota, Morihisa
Matsuura, Tomonori
Itoh, Takehito
Kin, Ryo
Katayama, Tomofumi
Endo, Katsuya
Takasu, Atsuko
Kogure, Takayuki
Murakami, Kazuhiro
Satoh, Kennichi
author_facet Koiwai, Akinobu
Hirota, Morihisa
Matsuura, Tomonori
Itoh, Takehito
Kin, Ryo
Katayama, Tomofumi
Endo, Katsuya
Takasu, Atsuko
Kogure, Takayuki
Murakami, Kazuhiro
Satoh, Kennichi
author_sort Koiwai, Akinobu
collection PubMed
description BACKGROUND AND AIM: Pancreatic ductal adenocarcinoma (PDAC) is a lethal cancer, partly because its early detection is difficult. This study aimed to identify computed tomography (CT) findings associated with PDAC prior to diagnosis. METHODS: Past CT images were retrospectively collected from the PDAC group (n = 54) and the control group (n = 90). The following imaging findings were compared: pancreatic mass, main pancreatic duct (MPD) dilatation with or without cutoff, cyst, chronic pancreatitis with calcification, partial parenchymal atrophy (PPA), and diffuse parenchymal atrophy (DPA). In the PDAC group, CT findings were examined during the pre‐diagnostic period and 6–36 months and 36–60 months before diagnosis. Multivariate analyses were performed using logistic regression. RESULTS: MPD dilatation with cutoff (P < 0.0001) and PPA (P = 0.023) were identified as significant imaging findings 6–36 months before diagnosis. DPA was identified as a novel imaging finding at 6–36 months (P = 0.003) and 36–60 months (P = 0.009) before diagnosis. CONCLUSION: DPA, MPD dilatation with cutoff, and PPA were identified as imaging findings associated with pre‐diagnostic PDAC.
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spelling pubmed-102902662023-06-25 Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study Koiwai, Akinobu Hirota, Morihisa Matsuura, Tomonori Itoh, Takehito Kin, Ryo Katayama, Tomofumi Endo, Katsuya Takasu, Atsuko Kogure, Takayuki Murakami, Kazuhiro Satoh, Kennichi JGH Open Original Articles BACKGROUND AND AIM: Pancreatic ductal adenocarcinoma (PDAC) is a lethal cancer, partly because its early detection is difficult. This study aimed to identify computed tomography (CT) findings associated with PDAC prior to diagnosis. METHODS: Past CT images were retrospectively collected from the PDAC group (n = 54) and the control group (n = 90). The following imaging findings were compared: pancreatic mass, main pancreatic duct (MPD) dilatation with or without cutoff, cyst, chronic pancreatitis with calcification, partial parenchymal atrophy (PPA), and diffuse parenchymal atrophy (DPA). In the PDAC group, CT findings were examined during the pre‐diagnostic period and 6–36 months and 36–60 months before diagnosis. Multivariate analyses were performed using logistic regression. RESULTS: MPD dilatation with cutoff (P < 0.0001) and PPA (P = 0.023) were identified as significant imaging findings 6–36 months before diagnosis. DPA was identified as a novel imaging finding at 6–36 months (P = 0.003) and 36–60 months (P = 0.009) before diagnosis. CONCLUSION: DPA, MPD dilatation with cutoff, and PPA were identified as imaging findings associated with pre‐diagnostic PDAC. Wiley Publishing Asia Pty Ltd 2023-06-02 /pmc/articles/PMC10290266/ /pubmed/37359111 http://dx.doi.org/10.1002/jgh3.12930 Text en © 2023 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Koiwai, Akinobu
Hirota, Morihisa
Matsuura, Tomonori
Itoh, Takehito
Kin, Ryo
Katayama, Tomofumi
Endo, Katsuya
Takasu, Atsuko
Kogure, Takayuki
Murakami, Kazuhiro
Satoh, Kennichi
Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study
title Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study
title_full Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study
title_fullStr Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study
title_full_unstemmed Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study
title_short Diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: A case–control study
title_sort diffuse pancreatic parenchymal atrophy, an imaging finding predictive of the development of pancreatic ductal adenocarcinoma: a case–control study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290266/
https://www.ncbi.nlm.nih.gov/pubmed/37359111
http://dx.doi.org/10.1002/jgh3.12930
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