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Autoimmune Pancreatitis and IgG4 Related Disease in Three Children

We report 3 children who presented with fever and abdominal pain, deranged liver function tests, and on abdominal ultrasound were found to have an enlarged pancreas, substantial abdominal lymphadenopathy, and extrahepatic biliary duct dilatation. After ruling out malignancy, probable immunoglobulin...

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Autores principales: Bolia, Rishi, Chong, Sze Yee, Coleman, Lee, MacGregor, Duncan, Hardikar, Winita, Oliver, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American College of Gastroenterology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018227/
https://www.ncbi.nlm.nih.gov/pubmed/27622194
http://dx.doi.org/10.14309/crj.2016.88
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author Bolia, Rishi
Chong, Sze Yee
Coleman, Lee
MacGregor, Duncan
Hardikar, Winita
Oliver, Mark R.
author_facet Bolia, Rishi
Chong, Sze Yee
Coleman, Lee
MacGregor, Duncan
Hardikar, Winita
Oliver, Mark R.
author_sort Bolia, Rishi
collection PubMed
description We report 3 children who presented with fever and abdominal pain, deranged liver function tests, and on abdominal ultrasound were found to have an enlarged pancreas, substantial abdominal lymphadenopathy, and extrahepatic biliary duct dilatation. After ruling out malignancy, probable immunoglobulin G4-related disease (IgG4RD) associated with autoimmune pancreatitis was considered. This condition was first described in the adults and often mimics pancreatic cancer. It can involve multiple organs, either synchronously or metachronously, and is rarely reported in children. The disorder mostly responds to corticosteroid therapy and other immune suppression. We highlight the difficulty in diagnosing autoimmune pancreatitis/IgG4-related disease in children and illustrate the difference between pediatric and adult presentation.
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spelling pubmed-50182272016-09-12 Autoimmune Pancreatitis and IgG4 Related Disease in Three Children Bolia, Rishi Chong, Sze Yee Coleman, Lee MacGregor, Duncan Hardikar, Winita Oliver, Mark R. ACG Case Rep J Case Report We report 3 children who presented with fever and abdominal pain, deranged liver function tests, and on abdominal ultrasound were found to have an enlarged pancreas, substantial abdominal lymphadenopathy, and extrahepatic biliary duct dilatation. After ruling out malignancy, probable immunoglobulin G4-related disease (IgG4RD) associated with autoimmune pancreatitis was considered. This condition was first described in the adults and often mimics pancreatic cancer. It can involve multiple organs, either synchronously or metachronously, and is rarely reported in children. The disorder mostly responds to corticosteroid therapy and other immune suppression. We highlight the difficulty in diagnosing autoimmune pancreatitis/IgG4-related disease in children and illustrate the difference between pediatric and adult presentation. American College of Gastroenterology 2016-08-31 /pmc/articles/PMC5018227/ /pubmed/27622194 http://dx.doi.org/10.14309/crj.2016.88 Text en Copyright © Bolia et al. This is an open-access article. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Case Report
Bolia, Rishi
Chong, Sze Yee
Coleman, Lee
MacGregor, Duncan
Hardikar, Winita
Oliver, Mark R.
Autoimmune Pancreatitis and IgG4 Related Disease in Three Children
title Autoimmune Pancreatitis and IgG4 Related Disease in Three Children
title_full Autoimmune Pancreatitis and IgG4 Related Disease in Three Children
title_fullStr Autoimmune Pancreatitis and IgG4 Related Disease in Three Children
title_full_unstemmed Autoimmune Pancreatitis and IgG4 Related Disease in Three Children
title_short Autoimmune Pancreatitis and IgG4 Related Disease in Three Children
title_sort autoimmune pancreatitis and igg4 related disease in three children
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018227/
https://www.ncbi.nlm.nih.gov/pubmed/27622194
http://dx.doi.org/10.14309/crj.2016.88
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