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Review on acute pancreatitis attributed to COVID-19 infection

The coronavirus disease 2019 (COVID-19) is known to cause gastrointestinal symptoms. Recent studies have revealed COVID-19-attributed acute pancreatitis (AP). However, clinical characteristics of COVID-19-attributed AP remain unclear. We performed a narrative review to elucidate relation between COV...

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Autores principales: Onoyama, Takumi, Koda, Hiroki, Hamamoto, Wataru, Kawahara, Shiho, Sakamoto, Yuri, Yamashita, Taro, Kurumi, Hiroki, Kawata, Soichiro, Takeda, Yohei, Matsumoto, Kazuya, Isomoto, Hajime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134139/
https://www.ncbi.nlm.nih.gov/pubmed/35664035
http://dx.doi.org/10.3748/wjg.v28.i19.2034
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author Onoyama, Takumi
Koda, Hiroki
Hamamoto, Wataru
Kawahara, Shiho
Sakamoto, Yuri
Yamashita, Taro
Kurumi, Hiroki
Kawata, Soichiro
Takeda, Yohei
Matsumoto, Kazuya
Isomoto, Hajime
author_facet Onoyama, Takumi
Koda, Hiroki
Hamamoto, Wataru
Kawahara, Shiho
Sakamoto, Yuri
Yamashita, Taro
Kurumi, Hiroki
Kawata, Soichiro
Takeda, Yohei
Matsumoto, Kazuya
Isomoto, Hajime
author_sort Onoyama, Takumi
collection PubMed
description The coronavirus disease 2019 (COVID-19) is known to cause gastrointestinal symptoms. Recent studies have revealed COVID-19-attributed acute pancreatitis (AP). However, clinical characteristics of COVID-19-attributed AP remain unclear. We performed a narrative review to elucidate relation between COVID-19 and AP using the PubMed database. Some basic and pathological reports revealed expression of angiotensin-converting enzyme 2 and transmembrane protease serine 2, key proteins that aid in the entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) into the pancreas. The experimental and pathological evaluation suggested that SARS-CoV-2 infects human endocrine and exocrine pancreas cells, and thus, SARS-CoV-2 may have a direct involvement in pancreatic disorders. Additionally, systemic inflammation, especially in children, may cause AP. Levels of immune mediators associated with AP, including interleukin (IL)-1β, IL-10, interferon-γ, monocyte chemotactic protein 1, and tumor necrosis factor-α are higher in the plasma of patients with COVID-19, that suggests an indirect involvement of the pancreas. In real-world settings, some clinical features of AP complicate COVID-19, such as a high complication rate of pancreatic necrosis, severe AP, and high mortality. However, clinical features of COVID-19-attributed AP remain uncertain due to insufficient research on etiologies of AP. Therefore, high-quality clinical studies and case reports that specify methods for differential diagnoses of other etiologies of AP are needed.
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spelling pubmed-91341392022-06-04 Review on acute pancreatitis attributed to COVID-19 infection Onoyama, Takumi Koda, Hiroki Hamamoto, Wataru Kawahara, Shiho Sakamoto, Yuri Yamashita, Taro Kurumi, Hiroki Kawata, Soichiro Takeda, Yohei Matsumoto, Kazuya Isomoto, Hajime World J Gastroenterol Review The coronavirus disease 2019 (COVID-19) is known to cause gastrointestinal symptoms. Recent studies have revealed COVID-19-attributed acute pancreatitis (AP). However, clinical characteristics of COVID-19-attributed AP remain unclear. We performed a narrative review to elucidate relation between COVID-19 and AP using the PubMed database. Some basic and pathological reports revealed expression of angiotensin-converting enzyme 2 and transmembrane protease serine 2, key proteins that aid in the entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) into the pancreas. The experimental and pathological evaluation suggested that SARS-CoV-2 infects human endocrine and exocrine pancreas cells, and thus, SARS-CoV-2 may have a direct involvement in pancreatic disorders. Additionally, systemic inflammation, especially in children, may cause AP. Levels of immune mediators associated with AP, including interleukin (IL)-1β, IL-10, interferon-γ, monocyte chemotactic protein 1, and tumor necrosis factor-α are higher in the plasma of patients with COVID-19, that suggests an indirect involvement of the pancreas. In real-world settings, some clinical features of AP complicate COVID-19, such as a high complication rate of pancreatic necrosis, severe AP, and high mortality. However, clinical features of COVID-19-attributed AP remain uncertain due to insufficient research on etiologies of AP. Therefore, high-quality clinical studies and case reports that specify methods for differential diagnoses of other etiologies of AP are needed. Baishideng Publishing Group Inc 2022-05-21 2022-05-21 /pmc/articles/PMC9134139/ /pubmed/35664035 http://dx.doi.org/10.3748/wjg.v28.i19.2034 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Review
Onoyama, Takumi
Koda, Hiroki
Hamamoto, Wataru
Kawahara, Shiho
Sakamoto, Yuri
Yamashita, Taro
Kurumi, Hiroki
Kawata, Soichiro
Takeda, Yohei
Matsumoto, Kazuya
Isomoto, Hajime
Review on acute pancreatitis attributed to COVID-19 infection
title Review on acute pancreatitis attributed to COVID-19 infection
title_full Review on acute pancreatitis attributed to COVID-19 infection
title_fullStr Review on acute pancreatitis attributed to COVID-19 infection
title_full_unstemmed Review on acute pancreatitis attributed to COVID-19 infection
title_short Review on acute pancreatitis attributed to COVID-19 infection
title_sort review on acute pancreatitis attributed to covid-19 infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134139/
https://www.ncbi.nlm.nih.gov/pubmed/35664035
http://dx.doi.org/10.3748/wjg.v28.i19.2034
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