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Pancreatitis, panniculitis and polyarthritis syndrome: A case report
BACKGROUND: Pancreatitis, panniculitis, and polyarthritis (PPP) syndrome is a rare form of pancreatic disease. It is characterized by bullous erythematous skin lesions and arthritis, and both are triggered by pancreatic malfunction. Few cases have been described in the literature thus far. Due to th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337007/ https://www.ncbi.nlm.nih.gov/pubmed/37449214 http://dx.doi.org/10.12998/wjcc.v11.i18.4412 |
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author | Pichler, Hannes Stumpner, Thomas Schiller, Dietmar Bischofreiter, Martin Ortmaier, Reinhold |
author_facet | Pichler, Hannes Stumpner, Thomas Schiller, Dietmar Bischofreiter, Martin Ortmaier, Reinhold |
author_sort | Pichler, Hannes |
collection | PubMed |
description | BACKGROUND: Pancreatitis, panniculitis, and polyarthritis (PPP) syndrome is a rare form of pancreatic disease. It is characterized by bullous erythematous skin lesions and arthritis, and both are triggered by pancreatic malfunction. Few cases have been described in the literature thus far. Due to the inconsistency in its clinical presentation, its diagnosis can be a challenge. Early therapy initiation is essential to reduce mortality; however, there is currently no gold standard for treatment. CASE SUMMARY: A 66-year-old polymorbid male patient presented with several superficial abscesses on both lower legs and painful swelling in the knee. Treatment for septic arthritis and septic skin infection over several weeks failed. His general condition deteriorated gradually and worsened with sudden onset of abdominal pain. A diagnosis of necrotizing pancreatitis was made. He subsequently underwent a laparotomy and drainage of the pancreas. Eventually, our patient improved, and his abdominal complaints, knee pain, and dermal lesions resolved. CONCLUSION: PPP syndrome is rare and easily misdiagnosed, as abdominal symptoms may be delayed or absent. Clinicians should consider PPP syndrome if they encounter refractory panniculitis in combination with joint infection. |
format | Online Article Text |
id | pubmed-10337007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-103370072023-07-13 Pancreatitis, panniculitis and polyarthritis syndrome: A case report Pichler, Hannes Stumpner, Thomas Schiller, Dietmar Bischofreiter, Martin Ortmaier, Reinhold World J Clin Cases Case Report BACKGROUND: Pancreatitis, panniculitis, and polyarthritis (PPP) syndrome is a rare form of pancreatic disease. It is characterized by bullous erythematous skin lesions and arthritis, and both are triggered by pancreatic malfunction. Few cases have been described in the literature thus far. Due to the inconsistency in its clinical presentation, its diagnosis can be a challenge. Early therapy initiation is essential to reduce mortality; however, there is currently no gold standard for treatment. CASE SUMMARY: A 66-year-old polymorbid male patient presented with several superficial abscesses on both lower legs and painful swelling in the knee. Treatment for septic arthritis and septic skin infection over several weeks failed. His general condition deteriorated gradually and worsened with sudden onset of abdominal pain. A diagnosis of necrotizing pancreatitis was made. He subsequently underwent a laparotomy and drainage of the pancreas. Eventually, our patient improved, and his abdominal complaints, knee pain, and dermal lesions resolved. CONCLUSION: PPP syndrome is rare and easily misdiagnosed, as abdominal symptoms may be delayed or absent. Clinicians should consider PPP syndrome if they encounter refractory panniculitis in combination with joint infection. Baishideng Publishing Group Inc 2023-06-26 2023-06-26 /pmc/articles/PMC10337007/ /pubmed/37449214 http://dx.doi.org/10.12998/wjcc.v11.i18.4412 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/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/ |
spellingShingle | Case Report Pichler, Hannes Stumpner, Thomas Schiller, Dietmar Bischofreiter, Martin Ortmaier, Reinhold Pancreatitis, panniculitis and polyarthritis syndrome: A case report |
title | Pancreatitis, panniculitis and polyarthritis syndrome: A case report |
title_full | Pancreatitis, panniculitis and polyarthritis syndrome: A case report |
title_fullStr | Pancreatitis, panniculitis and polyarthritis syndrome: A case report |
title_full_unstemmed | Pancreatitis, panniculitis and polyarthritis syndrome: A case report |
title_short | Pancreatitis, panniculitis and polyarthritis syndrome: A case report |
title_sort | pancreatitis, panniculitis and polyarthritis syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337007/ https://www.ncbi.nlm.nih.gov/pubmed/37449214 http://dx.doi.org/10.12998/wjcc.v11.i18.4412 |
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