Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location

We describe the first reported case of an IgG4-related autoimmune fibrosclerosing pseudotumour located in the stomach of a 75-year old woman presenting with weight loss and vomiting. A lesion was detected in the gastric body at endoscopy. Subsequent characterisation by CT was suggestive of a gastroi...

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Autores principales: Rollins, Katie E., Mehta, Samir P., O'Donovan, Maria, Safranek, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168566/
https://www.ncbi.nlm.nih.gov/pubmed/21991533
http://dx.doi.org/10.5402/2011/873087
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author Rollins, Katie E.
Mehta, Samir P.
O'Donovan, Maria
Safranek, Peter M.
author_facet Rollins, Katie E.
Mehta, Samir P.
O'Donovan, Maria
Safranek, Peter M.
author_sort Rollins, Katie E.
collection PubMed
description We describe the first reported case of an IgG4-related autoimmune fibrosclerosing pseudotumour located in the stomach of a 75-year old woman presenting with weight loss and vomiting. A lesion was detected in the gastric body at endoscopy. Subsequent characterisation by CT was suggestive of a gastrointestinal stromal tumour. Following laparoscopic resection, the patient recovered uneventfully. Histological examination of the resected specimen revealed an IgG4-related fibrosclerosing pseudotumour, a novel location for this histopathological entity.
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spelling pubmed-31685662011-10-11 Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location Rollins, Katie E. Mehta, Samir P. O'Donovan, Maria Safranek, Peter M. ISRN Gastroenterol Case Report We describe the first reported case of an IgG4-related autoimmune fibrosclerosing pseudotumour located in the stomach of a 75-year old woman presenting with weight loss and vomiting. A lesion was detected in the gastric body at endoscopy. Subsequent characterisation by CT was suggestive of a gastrointestinal stromal tumour. Following laparoscopic resection, the patient recovered uneventfully. Histological examination of the resected specimen revealed an IgG4-related fibrosclerosing pseudotumour, a novel location for this histopathological entity. International Scholarly Research Network 2011 2010-11-07 /pmc/articles/PMC3168566/ /pubmed/21991533 http://dx.doi.org/10.5402/2011/873087 Text en Copyright © 2011 Katie E. Rollins et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rollins, Katie E.
Mehta, Samir P.
O'Donovan, Maria
Safranek, Peter M.
Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location
title Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location
title_full Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location
title_fullStr Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location
title_full_unstemmed Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location
title_short Gastric IgG4-Related Autoimmune Fibrosclerosing Pseudotumour: A Novel Location
title_sort gastric igg4-related autoimmune fibrosclerosing pseudotumour: a novel location
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168566/
https://www.ncbi.nlm.nih.gov/pubmed/21991533
http://dx.doi.org/10.5402/2011/873087
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