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Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report
Introduction: Granulomatosis with polyangiitis (GPA) vasculitis typically involves upper and lower airways and kidneys. Gastrointestinal involvement is rare, clinically reported as esophageal involvement, gastrointestinal hemorrhage, intestinal perforation, colitis, and pancreatitis. Case presentati...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686004/ https://www.ncbi.nlm.nih.gov/pubmed/38033412 http://dx.doi.org/10.1093/omcr/omad127 |
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author | Khalayli, Naram Aldeeb, Maria Abouharb, Dani Abouharb, Lana Kudsi, Maysoun |
author_facet | Khalayli, Naram Aldeeb, Maria Abouharb, Dani Abouharb, Lana Kudsi, Maysoun |
author_sort | Khalayli, Naram |
collection | PubMed |
description | Introduction: Granulomatosis with polyangiitis (GPA) vasculitis typically involves upper and lower airways and kidneys. Gastrointestinal involvement is rare, clinically reported as esophageal involvement, gastrointestinal hemorrhage, intestinal perforation, colitis, and pancreatitis. Case presentation: We present a 36 old man, with intestinal perforation, laterally diagnosed as granulomatosis with polyangiitis. Discussion: Only a few cases of intestinal perforation have been reported in the medical literature. GI symptoms may be present after the disease diagnosis in years. Intestinal perforation usually required surgery. The frequent kidney involvement of GPA is rapidly progressive glomerulonephritis, presented as acute kidney injury, usually accompanied by GI symptoms. Cyclophosphamide plus corticosteroids remain the effective therapy. The patient with GPA had a normal life expectancy due to the advances in treatment. Renal involvement and GI manifestations are considered bad prognosis predictors. Conclusion: This case report illustrates the need to consider intestinal perforation in patients with granulomatosis with polyangiitis, early surgical intervention and appropriate immunosuppressive therapy can be lifesaving. |
format | Online Article Text |
id | pubmed-10686004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106860042023-11-30 Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report Khalayli, Naram Aldeeb, Maria Abouharb, Dani Abouharb, Lana Kudsi, Maysoun Oxf Med Case Reports Case Report Introduction: Granulomatosis with polyangiitis (GPA) vasculitis typically involves upper and lower airways and kidneys. Gastrointestinal involvement is rare, clinically reported as esophageal involvement, gastrointestinal hemorrhage, intestinal perforation, colitis, and pancreatitis. Case presentation: We present a 36 old man, with intestinal perforation, laterally diagnosed as granulomatosis with polyangiitis. Discussion: Only a few cases of intestinal perforation have been reported in the medical literature. GI symptoms may be present after the disease diagnosis in years. Intestinal perforation usually required surgery. The frequent kidney involvement of GPA is rapidly progressive glomerulonephritis, presented as acute kidney injury, usually accompanied by GI symptoms. Cyclophosphamide plus corticosteroids remain the effective therapy. The patient with GPA had a normal life expectancy due to the advances in treatment. Renal involvement and GI manifestations are considered bad prognosis predictors. Conclusion: This case report illustrates the need to consider intestinal perforation in patients with granulomatosis with polyangiitis, early surgical intervention and appropriate immunosuppressive therapy can be lifesaving. Oxford University Press 2023-11-28 /pmc/articles/PMC10686004/ /pubmed/38033412 http://dx.doi.org/10.1093/omcr/omad127 Text en © The Author(s) 2023. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Khalayli, Naram Aldeeb, Maria Abouharb, Dani Abouharb, Lana Kudsi, Maysoun Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
title | Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
title_full | Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
title_fullStr | Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
title_full_unstemmed | Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
title_short | Intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
title_sort | intestinal perforation as a first presentation of granulomatosis with polyangiitis: unusual case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686004/ https://www.ncbi.nlm.nih.gov/pubmed/38033412 http://dx.doi.org/10.1093/omcr/omad127 |
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