Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst

Pancreatic cystic lesions comprise diverse entities with different histopathological characteristics. Differential diagnosis is often challenging. Autoimmune pancreatitis (AIP) is usually not considered an underlying pathology in the differential diagnosis of peri-/pancreatic pseudo-/cystic lesions....

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Main Authors: Felix Hesse, Rickmer Braren, Roland M. Schmid, Veit Phillip
Format: Article
Language:English
Published: Karger Publishers 2019-04-01
Series:Case Reports in Gastroenterology
Subjects:
Online Access:https://www.karger.com/Article/FullText/499444
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spelling doaj-d434fad55c9b48e89550ce56cc12ec7e2020-11-25T01:22:19ZengKarger PublishersCase Reports in Gastroenterology1662-06312019-04-0113119519910.1159/000499444499444Autoimmune Pancreatitis Type 1 Associated with a Pancreatic PseudocystFelix HesseRickmer BrarenRoland M. SchmidVeit PhillipPancreatic cystic lesions comprise diverse entities with different histopathological characteristics. Differential diagnosis is often challenging. Autoimmune pancreatitis (AIP) is usually not considered an underlying pathology in the differential diagnosis of peri-/pancreatic pseudo-/cystic lesions. We report the case of a 73-year-old male with diffuse pancreatic enlargement and an adjacent cystic lesion (60 × 80 mm) on computed tomography scan. Based on these imaging findings and an elevated serum IgG4 concentration, AIP complicated by a pancreatic pseudocyst was diagnosed, and treatment with glucocorticoids was started. Regular follow-ups showed a good response to treatment with regression of the pancreatic pseudocyst and remittent pancreatic swelling.https://www.karger.com/Article/FullText/499444Autoimmune pancreatitisCorticosteroidPancreatic pseudocyst
collection DOAJ
language English
format Article
sources DOAJ
author Felix Hesse
Rickmer Braren
Roland M. Schmid
Veit Phillip
spellingShingle Felix Hesse
Rickmer Braren
Roland M. Schmid
Veit Phillip
Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst
Case Reports in Gastroenterology
Autoimmune pancreatitis
Corticosteroid
Pancreatic pseudocyst
author_facet Felix Hesse
Rickmer Braren
Roland M. Schmid
Veit Phillip
author_sort Felix Hesse
title Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst
title_short Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst
title_full Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst
title_fullStr Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst
title_full_unstemmed Autoimmune Pancreatitis Type 1 Associated with a Pancreatic Pseudocyst
title_sort autoimmune pancreatitis type 1 associated with a pancreatic pseudocyst
publisher Karger Publishers
series Case Reports in Gastroenterology
issn 1662-0631
publishDate 2019-04-01
description Pancreatic cystic lesions comprise diverse entities with different histopathological characteristics. Differential diagnosis is often challenging. Autoimmune pancreatitis (AIP) is usually not considered an underlying pathology in the differential diagnosis of peri-/pancreatic pseudo-/cystic lesions. We report the case of a 73-year-old male with diffuse pancreatic enlargement and an adjacent cystic lesion (60 × 80 mm) on computed tomography scan. Based on these imaging findings and an elevated serum IgG4 concentration, AIP complicated by a pancreatic pseudocyst was diagnosed, and treatment with glucocorticoids was started. Regular follow-ups showed a good response to treatment with regression of the pancreatic pseudocyst and remittent pancreatic swelling.
topic Autoimmune pancreatitis
Corticosteroid
Pancreatic pseudocyst
url https://www.karger.com/Article/FullText/499444
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AT rickmerbraren autoimmunepancreatitistype1associatedwithapancreaticpseudocyst
AT rolandmschmid autoimmunepancreatitistype1associatedwithapancreaticpseudocyst
AT veitphillip autoimmunepancreatitistype1associatedwithapancreaticpseudocyst
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