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Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis

Granulomatosis with polyangiitis (GPA) is a rare necrotizing antineutrophil cytoplasmic antibody-associated vasculitis characterized by inflammation in small-sized arteries. Gastrointestinal involvement is exceedingly rare in GPA. Here, we present a case of recurrent acute pancreatitis as the initia...

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Autores principales: Youssef, Michael, Sedarous, Mary, Grin, Andrea, Chung, Andrew, Hookey, Lawrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915951/
https://www.ncbi.nlm.nih.gov/pubmed/36788786
http://dx.doi.org/10.14309/crj.0000000000000986
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author Youssef, Michael
Sedarous, Mary
Grin, Andrea
Chung, Andrew
Hookey, Lawrence
author_facet Youssef, Michael
Sedarous, Mary
Grin, Andrea
Chung, Andrew
Hookey, Lawrence
author_sort Youssef, Michael
collection PubMed
description Granulomatosis with polyangiitis (GPA) is a rare necrotizing antineutrophil cytoplasmic antibody-associated vasculitis characterized by inflammation in small-sized arteries. Gastrointestinal involvement is exceedingly rare in GPA. Here, we present a case of recurrent acute pancreatitis as the initial presentation of GPA. The diagnosis was made based on radiological and pathological findings of acute pancreatitis in conjunction with positive anti-PR3 antibody which is strongly associated with GPA. Systemic vasculitides are rare but important to consider in cases of idiopathic acute pancreatitis. Early diagnosis and therapy allow for high rates of remission and improved survival rates.
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spelling pubmed-99159512023-02-13 Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis Youssef, Michael Sedarous, Mary Grin, Andrea Chung, Andrew Hookey, Lawrence ACG Case Rep J Case Report Granulomatosis with polyangiitis (GPA) is a rare necrotizing antineutrophil cytoplasmic antibody-associated vasculitis characterized by inflammation in small-sized arteries. Gastrointestinal involvement is exceedingly rare in GPA. Here, we present a case of recurrent acute pancreatitis as the initial presentation of GPA. The diagnosis was made based on radiological and pathological findings of acute pancreatitis in conjunction with positive anti-PR3 antibody which is strongly associated with GPA. Systemic vasculitides are rare but important to consider in cases of idiopathic acute pancreatitis. Early diagnosis and therapy allow for high rates of remission and improved survival rates. Wolters Kluwer 2023-02-10 /pmc/articles/PMC9915951/ /pubmed/36788786 http://dx.doi.org/10.14309/crj.0000000000000986 Text en © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Youssef, Michael
Sedarous, Mary
Grin, Andrea
Chung, Andrew
Hookey, Lawrence
Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis
title Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis
title_full Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis
title_fullStr Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis
title_full_unstemmed Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis
title_short Acute Pancreatitis as a First Presentation of Granulomatosis With Polyangiitis
title_sort acute pancreatitis as a first presentation of granulomatosis with polyangiitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915951/
https://www.ncbi.nlm.nih.gov/pubmed/36788786
http://dx.doi.org/10.14309/crj.0000000000000986
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