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Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm
A 78-year-old woman was admitted to our hospital with a pancreatic tumor, incidentally discovered in an abdominal ultrasound exam. She was asymptomatic and without any previous personal pathological condition. The computed tomography (CT) and the magnetic resonance imaging (MRI) scan showed a mass l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600032/ https://www.ncbi.nlm.nih.gov/pubmed/31275087 http://dx.doi.org/10.1159/000501064 |
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author | Baião, José Miguel Martins, Rui Miguel Correia, João Guardado Jordão, Daniel Vieira Caroço, Teresa Caetano Oliveira, Rui Agostinho, Paulo Gil Ferrão, Henrique |
author_facet | Baião, José Miguel Martins, Rui Miguel Correia, João Guardado Jordão, Daniel Vieira Caroço, Teresa Caetano Oliveira, Rui Agostinho, Paulo Gil Ferrão, Henrique |
author_sort | Baião, José Miguel |
collection | PubMed |
description | A 78-year-old woman was admitted to our hospital with a pancreatic tumor, incidentally discovered in an abdominal ultrasound exam. She was asymptomatic and without any previous personal pathological condition. The computed tomography (CT) and the magnetic resonance imaging (MRI) scan showed a mass lesion of 4 cm in diameter, located in the pancreatic body, conditioning the invasion of the splenic vein. The patient was admitted to surgery. During the laparotomy, we found a tumoral lesion highly suspicious of pancreatic neoplasia located in the transition of the head/body of the pancreas, with an invasion of the portal vein and several peri-regional lymph nodes. We performed biopsies of the pancreatic mass and lymphadenectomy of the peri-regional pancreatic lymph nodes. Histological analysis found an inflammatory pseudotumor of the head/body of the pancreas, without signals of malign epithelial neoplasm and also without criteria for immunoglobulin G4-related disease. During the follow-up, a PET/CT and MRI confirmed that the pancreatic lesion had disappeared without any treatment. Inflammatory pseudotumor of the pancreas is a rare entity not fully understood. Despite this, the administration of corticosteroids and immunosuppressive therapy could be taken into consideration as the disease carries a risk. |
format | Online Article Text |
id | pubmed-6600032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-66000322019-07-03 Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm Baião, José Miguel Martins, Rui Miguel Correia, João Guardado Jordão, Daniel Vieira Caroço, Teresa Caetano Oliveira, Rui Agostinho, Paulo Gil Ferrão, Henrique Case Rep Gastroenterol Single Case A 78-year-old woman was admitted to our hospital with a pancreatic tumor, incidentally discovered in an abdominal ultrasound exam. She was asymptomatic and without any previous personal pathological condition. The computed tomography (CT) and the magnetic resonance imaging (MRI) scan showed a mass lesion of 4 cm in diameter, located in the pancreatic body, conditioning the invasion of the splenic vein. The patient was admitted to surgery. During the laparotomy, we found a tumoral lesion highly suspicious of pancreatic neoplasia located in the transition of the head/body of the pancreas, with an invasion of the portal vein and several peri-regional lymph nodes. We performed biopsies of the pancreatic mass and lymphadenectomy of the peri-regional pancreatic lymph nodes. Histological analysis found an inflammatory pseudotumor of the head/body of the pancreas, without signals of malign epithelial neoplasm and also without criteria for immunoglobulin G4-related disease. During the follow-up, a PET/CT and MRI confirmed that the pancreatic lesion had disappeared without any treatment. Inflammatory pseudotumor of the pancreas is a rare entity not fully understood. Despite this, the administration of corticosteroids and immunosuppressive therapy could be taken into consideration as the disease carries a risk. S. Karger AG 2019-06-13 /pmc/articles/PMC6600032/ /pubmed/31275087 http://dx.doi.org/10.1159/000501064 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Single Case Baião, José Miguel Martins, Rui Miguel Correia, João Guardado Jordão, Daniel Vieira Caroço, Teresa Caetano Oliveira, Rui Agostinho, Paulo Gil Ferrão, Henrique Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm |
title | Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm |
title_full | Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm |
title_fullStr | Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm |
title_full_unstemmed | Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm |
title_short | Inflammatory Pseudotumor of the Pancreas Mimicking a Pancreatic Neoplasm |
title_sort | inflammatory pseudotumor of the pancreas mimicking a pancreatic neoplasm |
topic | Single Case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600032/ https://www.ncbi.nlm.nih.gov/pubmed/31275087 http://dx.doi.org/10.1159/000501064 |
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