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Inflammatory pseudotumor of spleen

Inflammatory pseudotumor (IPT) is an uncommon tumor and its occurrence in spleen is rare. This tumor is composed of proliferation of spindle cells of unknown origin and etiology that mimic other tumors at clinical and histological evaluation. The most surmising etiology is Epstein Barr virus (EBV) a...

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Autores principales: Rajabi, Parvin, Noorollahi, Hasan, Hani, Mohsen, Bagheri, Marzie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928915/
https://www.ncbi.nlm.nih.gov/pubmed/24592376
http://dx.doi.org/10.4103/2277-9175.124679
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author Rajabi, Parvin
Noorollahi, Hasan
Hani, Mohsen
Bagheri, Marzie
author_facet Rajabi, Parvin
Noorollahi, Hasan
Hani, Mohsen
Bagheri, Marzie
author_sort Rajabi, Parvin
collection PubMed
description Inflammatory pseudotumor (IPT) is an uncommon tumor and its occurrence in spleen is rare. This tumor is composed of proliferation of spindle cells of unknown origin and etiology that mimic other tumors at clinical and histological evaluation. The most surmising etiology is Epstein Barr virus (EBV) and the most suspected origin is myofibroblasts, hence its synonym is “inflammatory myofibroblastic tumor.” The clinical appearance of tumor is related to its location but the most ones are abdominal pain, fever and weight loss. Surgical removal for this lesion is treatment of choice and there is few reported case with recurrence and metastasis. Herein we report a 63-year-old female patient with and abdominal discomfort that primary paraclinical investigations had been showed splenic mass and therefore surgical treatment was performed for her. Microscopic examination suggest some different diagnosis such as IPT, thus immunohistochemical staining was perform to confirm the diagnosis and rule out the others.
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spelling pubmed-39289152014-03-03 Inflammatory pseudotumor of spleen Rajabi, Parvin Noorollahi, Hasan Hani, Mohsen Bagheri, Marzie Adv Biomed Res Case Report Inflammatory pseudotumor (IPT) is an uncommon tumor and its occurrence in spleen is rare. This tumor is composed of proliferation of spindle cells of unknown origin and etiology that mimic other tumors at clinical and histological evaluation. The most surmising etiology is Epstein Barr virus (EBV) and the most suspected origin is myofibroblasts, hence its synonym is “inflammatory myofibroblastic tumor.” The clinical appearance of tumor is related to its location but the most ones are abdominal pain, fever and weight loss. Surgical removal for this lesion is treatment of choice and there is few reported case with recurrence and metastasis. Herein we report a 63-year-old female patient with and abdominal discomfort that primary paraclinical investigations had been showed splenic mass and therefore surgical treatment was performed for her. Microscopic examination suggest some different diagnosis such as IPT, thus immunohistochemical staining was perform to confirm the diagnosis and rule out the others. Medknow Publications & Media Pvt Ltd 2014-01-09 /pmc/articles/PMC3928915/ /pubmed/24592376 http://dx.doi.org/10.4103/2277-9175.124679 Text en Copyright: © 2014 Rajabi. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Rajabi, Parvin
Noorollahi, Hasan
Hani, Mohsen
Bagheri, Marzie
Inflammatory pseudotumor of spleen
title Inflammatory pseudotumor of spleen
title_full Inflammatory pseudotumor of spleen
title_fullStr Inflammatory pseudotumor of spleen
title_full_unstemmed Inflammatory pseudotumor of spleen
title_short Inflammatory pseudotumor of spleen
title_sort inflammatory pseudotumor of spleen
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928915/
https://www.ncbi.nlm.nih.gov/pubmed/24592376
http://dx.doi.org/10.4103/2277-9175.124679
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