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Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor

A 79-year-old man was admitted with asymptomatic elevation of liver enzymes and tumor markers. Abdominal contrast-enhanced computed tomography demonstrated swelling of the pancreatic head, and additional blood test showed raised IgG4 levels. Histological examination by endoscopic ultrasonography (EU...

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Autores principales: Ezaki, Takeshi, Masuda, Atsuhiro, Shiomi, Hideyuki, Nakagawa, Takashi, Sofue, Keitaro, Toyama, Hirochika, Zen, Yoh, Kodama, Yuzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600027/
https://www.ncbi.nlm.nih.gov/pubmed/31275090
http://dx.doi.org/10.1159/000500477
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author Ezaki, Takeshi
Masuda, Atsuhiro
Shiomi, Hideyuki
Nakagawa, Takashi
Sofue, Keitaro
Toyama, Hirochika
Zen, Yoh
Kodama, Yuzo
author_facet Ezaki, Takeshi
Masuda, Atsuhiro
Shiomi, Hideyuki
Nakagawa, Takashi
Sofue, Keitaro
Toyama, Hirochika
Zen, Yoh
Kodama, Yuzo
author_sort Ezaki, Takeshi
collection PubMed
description A 79-year-old man was admitted with asymptomatic elevation of liver enzymes and tumor markers. Abdominal contrast-enhanced computed tomography demonstrated swelling of the pancreatic head, and additional blood test showed raised IgG4 levels. Histological examination by endoscopic ultrasonography (EUS)-guided fine needle aspiration for pancreatic head mass revealed storiform fibrosis and IgG4-positive plasma cell infiltration. We diagnosed this case as type 1 autoimmune pancreatitis (AIP). In addition, there was a cystic lesion in the pancreatic body apart from the pancreatic head mass. A mural nodule in the multilocular cyst was detected by EUS, and there was positive uptake of fluorodeoxyglucose in positron emission tomography/magnetic resonance imaging. The preoperative diagnosis of this cystic lesion was intraductal papillary mucinous carcinoma, and distal pancreatomy was performed. Histopathological findings showed various sizes of retention cysts caused by IgG4-positive plasma cell infiltration around the pancreatic branch ducts. The mural nodule was a fibrotic mass with diffuse infiltration of IgG4-positive cells. This cystic lesion mimicking malignant cystic neoplasm occurred in relation to AIP. This case provided important information helping to understand the mechanism of formation of mural nodules in multilocular cysts in patients with type 1 AIP.
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spelling pubmed-66000272019-07-03 Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor Ezaki, Takeshi Masuda, Atsuhiro Shiomi, Hideyuki Nakagawa, Takashi Sofue, Keitaro Toyama, Hirochika Zen, Yoh Kodama, Yuzo Case Rep Gastroenterol Single Case A 79-year-old man was admitted with asymptomatic elevation of liver enzymes and tumor markers. Abdominal contrast-enhanced computed tomography demonstrated swelling of the pancreatic head, and additional blood test showed raised IgG4 levels. Histological examination by endoscopic ultrasonography (EUS)-guided fine needle aspiration for pancreatic head mass revealed storiform fibrosis and IgG4-positive plasma cell infiltration. We diagnosed this case as type 1 autoimmune pancreatitis (AIP). In addition, there was a cystic lesion in the pancreatic body apart from the pancreatic head mass. A mural nodule in the multilocular cyst was detected by EUS, and there was positive uptake of fluorodeoxyglucose in positron emission tomography/magnetic resonance imaging. The preoperative diagnosis of this cystic lesion was intraductal papillary mucinous carcinoma, and distal pancreatomy was performed. Histopathological findings showed various sizes of retention cysts caused by IgG4-positive plasma cell infiltration around the pancreatic branch ducts. The mural nodule was a fibrotic mass with diffuse infiltration of IgG4-positive cells. This cystic lesion mimicking malignant cystic neoplasm occurred in relation to AIP. This case provided important information helping to understand the mechanism of formation of mural nodules in multilocular cysts in patients with type 1 AIP. S. Karger AG 2019-06-14 /pmc/articles/PMC6600027/ /pubmed/31275090 http://dx.doi.org/10.1159/000500477 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case
Ezaki, Takeshi
Masuda, Atsuhiro
Shiomi, Hideyuki
Nakagawa, Takashi
Sofue, Keitaro
Toyama, Hirochika
Zen, Yoh
Kodama, Yuzo
Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor
title Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor
title_full Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor
title_fullStr Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor
title_full_unstemmed Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor
title_short Type 1 Autoimmune Pancreatitis with Imaging Appearance Similar to That of Malignant Cystic Tumor
title_sort type 1 autoimmune pancreatitis with imaging appearance similar to that of malignant cystic tumor
topic Single Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600027/
https://www.ncbi.nlm.nih.gov/pubmed/31275090
http://dx.doi.org/10.1159/000500477
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