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IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review
BACKGROUND: IgG4-related disease involvement of the digestive tract is very rare. In few reported cases of isolated gastric/duodenal IgG4-related disease, none of which resulted in luminal obstruction. CASE PRESENTATION: A 59 years old female presented with longstanding gastrointestinal symptoms. CT...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454001/ https://www.ncbi.nlm.nih.gov/pubmed/34544364 http://dx.doi.org/10.1186/s12876-021-01927-x |
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author | Chen, Lina Almudaires, Abdulaziz Alzahrani, May Qumosani, Karim Chakrabarti, Subrata |
author_facet | Chen, Lina Almudaires, Abdulaziz Alzahrani, May Qumosani, Karim Chakrabarti, Subrata |
author_sort | Chen, Lina |
collection | PubMed |
description | BACKGROUND: IgG4-related disease involvement of the digestive tract is very rare. In few reported cases of isolated gastric/duodenal IgG4-related disease, none of which resulted in luminal obstruction. CASE PRESENTATION: A 59 years old female presented with longstanding gastrointestinal symptoms. CT showed mural thickening of the proximal duodenum. Gastroscopy showed antral ulcer extending into the duodenum with outlet obstruction and biopsy showed acute on chronic duodenitis. Whipple’s procedure was performed and IgG4-related disease was diagnosed on final pathology. Symptoms were revolved on mycophenolate mofetil and prednisone with no recurrence. CONCLUSIONS: Our case is the only reported case with gastric outlet obstruction secondary to gastroduodenal IgG4-related disease. The diagnosis should be considered in the differential diagnosis of unexplained duodenal stricture, gastric outlet obstruction or gastrointestinal ulceration. IgG4-related disease usually responds to steroids but long-term response rates to steroid-sparing agents, especially in the subset of patients with luminal IgG4-related disease remains to be determined. |
format | Online Article Text |
id | pubmed-8454001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84540012021-09-21 IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review Chen, Lina Almudaires, Abdulaziz Alzahrani, May Qumosani, Karim Chakrabarti, Subrata BMC Gastroenterol Case Report BACKGROUND: IgG4-related disease involvement of the digestive tract is very rare. In few reported cases of isolated gastric/duodenal IgG4-related disease, none of which resulted in luminal obstruction. CASE PRESENTATION: A 59 years old female presented with longstanding gastrointestinal symptoms. CT showed mural thickening of the proximal duodenum. Gastroscopy showed antral ulcer extending into the duodenum with outlet obstruction and biopsy showed acute on chronic duodenitis. Whipple’s procedure was performed and IgG4-related disease was diagnosed on final pathology. Symptoms were revolved on mycophenolate mofetil and prednisone with no recurrence. CONCLUSIONS: Our case is the only reported case with gastric outlet obstruction secondary to gastroduodenal IgG4-related disease. The diagnosis should be considered in the differential diagnosis of unexplained duodenal stricture, gastric outlet obstruction or gastrointestinal ulceration. IgG4-related disease usually responds to steroids but long-term response rates to steroid-sparing agents, especially in the subset of patients with luminal IgG4-related disease remains to be determined. BioMed Central 2021-09-20 /pmc/articles/PMC8454001/ /pubmed/34544364 http://dx.doi.org/10.1186/s12876-021-01927-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Chen, Lina Almudaires, Abdulaziz Alzahrani, May Qumosani, Karim Chakrabarti, Subrata IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
title | IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
title_full | IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
title_fullStr | IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
title_full_unstemmed | IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
title_short | IgG4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
title_sort | igg4-related disease as a rare cause of gastric outlet obstruction: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454001/ https://www.ncbi.nlm.nih.gov/pubmed/34544364 http://dx.doi.org/10.1186/s12876-021-01927-x |
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