Editorial
Copyright ©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 21, 2024; 30(7): 614-623
Published online Feb 21, 2024. doi: 10.3748/wjg.v30.i7.614
Pathophysiology of severe gallstone pancreatitis: A new paradigm
Masatoshi Isogai
Masatoshi Isogai, Clinic IB, Ibi 501-0614, Gifu, Japan
Masatoshi Isogai, Department of Surgery, Nawa Hospital, Ogaki 503-0893, Gifu, Japan
Author contributions: Isogai M conceived the idea for the manuscript, reviewed the literature, drafted the manuscript, and approved the final version of the article.
Conflict-of-interest statement: There is no conflict of interest to declare.
Open-Access: 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. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Masatoshi Isogai, MD, Director, Clinic IB, No. 657-1 Ibigawa-cho Nagara, Ibi 501-0614, Gifu, Japan. masatoshi.isogai@gmail.com
Received: October 18, 2023
Peer-review started: October 18, 2023
First decision: December 11, 2023
Revised: December 16, 2023
Accepted: January 18, 2024
Article in press: January 18, 2024
Published online: February 21, 2024
Processing time: 125 Days and 23.5 Hours
Abstract

Severe gallstone pancreatitis (GSP) refractory to maximum conservative therapy has wide clinical variations, and its pathophysiology remains controversial. This Editorial aimed to investigate the pathophysiology of severe disease based on Opie’s theories of obstruction, the common channel, and duodenal reflux and describe its types. Severe GSP might be a hybrid disease with pathology polarized between acute cholangitis with mild pancreatitis (biliary type) and necrotizing pancreatitis uncomplicated with biliary tract disease (pancreatic type), in which hepatobiliary and pancreatic lesion severity is inversely related to the presence or absence of impacted ampullary stones. Severe GSP is caused by stones that are persistently impacted at the ampulla with biliopancreatic obstruction (biliary type), and probably, stones that are either temporarily lodged at the duodenal orifice or passed into the duodenum, thereby permitting reflux of bile or possible duodenal contents into the pancreas (pancreas type). When the status of the stones and the presence or absence of impacted ampullary stones with biliopancreatic obstruction are determined, the clinical course and outcome can be predicted. Gallstones represent the main cause of acute pancreatitis globally, and clinicians are expected to encounter GSP more often. Awareness of the etiology and pathogenesis of severe disease is mandatory.

Keywords: Gallstone pancreatitis; Biliary pancreatitis; Gallstone hepatitis; Acute cholangitis; Necrotizing pancreatitis; Pathophysiology

Core Tip: Gallstones represent the main cause of acute pancreatitis globally, and awareness of the etiology and pathogenesis of severe disease is mandatory. Based on the present study aimed to clarify the pathophysiology of severe disease from clinicopathological and historical points of view, severe gallstone pancreatitis may be a hybrid disease with pathology polarized between acute cholangitis and necrotizing pancreatitis in which the severity of hepatobiliary and pancreatic lesions is inversely related to the presence or absence of impacted ampullary stones with biliopancreatic obstruction. When the status of the stones is determined, the clinical course and outcome can be predicted.