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Inflammatory myofibroblastic tumor of the spleen: a case report

Inflammatory myofibroblastic tumors (IMTs), otherwise known as the inflammatory pseudotumor, is a rare solid mesenchymal tumor, simulating malignant neoplasms, histologically characterized by the proliferation of spindle cells in a fibrous myxoid stroma containing inflammatory cells. CT and MR imagi...

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Autores principales: Bettach, H., Alami, B., Boubbou, M., Chbani, L., Maâroufi, M., Lamrani, MY Alaoui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377435/
https://www.ncbi.nlm.nih.gov/pubmed/34457099
http://dx.doi.org/10.1016/j.radcr.2021.07.029
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author Bettach, H.
Alami, B.
Boubbou, M.
Chbani, L.
Maâroufi, M.
Lamrani, MY Alaoui
author_facet Bettach, H.
Alami, B.
Boubbou, M.
Chbani, L.
Maâroufi, M.
Lamrani, MY Alaoui
author_sort Bettach, H.
collection PubMed
description Inflammatory myofibroblastic tumors (IMTs), otherwise known as the inflammatory pseudotumor, is a rare solid mesenchymal tumor, simulating malignant neoplasms, histologically characterized by the proliferation of spindle cells in a fibrous myxoid stroma containing inflammatory cells. CT and MR imaging are the most used tools in their assessment. Clinical features are nonspecific and depend on the localization of the tumor, radiologic findings are polymorphic and no-conclusive and present a diagnostic challenge to the radiologist. Although histology remains obligatory for the final diagnosis. Heren, we report a case of splenic IMT with histological correlation.
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spelling pubmed-83774352021-08-26 Inflammatory myofibroblastic tumor of the spleen: a case report Bettach, H. Alami, B. Boubbou, M. Chbani, L. Maâroufi, M. Lamrani, MY Alaoui Radiol Case Rep Case Report Inflammatory myofibroblastic tumors (IMTs), otherwise known as the inflammatory pseudotumor, is a rare solid mesenchymal tumor, simulating malignant neoplasms, histologically characterized by the proliferation of spindle cells in a fibrous myxoid stroma containing inflammatory cells. CT and MR imaging are the most used tools in their assessment. Clinical features are nonspecific and depend on the localization of the tumor, radiologic findings are polymorphic and no-conclusive and present a diagnostic challenge to the radiologist. Although histology remains obligatory for the final diagnosis. Heren, we report a case of splenic IMT with histological correlation. Elsevier 2021-08-16 /pmc/articles/PMC8377435/ /pubmed/34457099 http://dx.doi.org/10.1016/j.radcr.2021.07.029 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Bettach, H.
Alami, B.
Boubbou, M.
Chbani, L.
Maâroufi, M.
Lamrani, MY Alaoui
Inflammatory myofibroblastic tumor of the spleen: a case report
title Inflammatory myofibroblastic tumor of the spleen: a case report
title_full Inflammatory myofibroblastic tumor of the spleen: a case report
title_fullStr Inflammatory myofibroblastic tumor of the spleen: a case report
title_full_unstemmed Inflammatory myofibroblastic tumor of the spleen: a case report
title_short Inflammatory myofibroblastic tumor of the spleen: a case report
title_sort inflammatory myofibroblastic tumor of the spleen: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377435/
https://www.ncbi.nlm.nih.gov/pubmed/34457099
http://dx.doi.org/10.1016/j.radcr.2021.07.029
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