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An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement

Extramedullary hematopoiesis in the posterior mediastinum is rare. Our case interested a 28‐year‐old man with a history of eosinophilia with FIP1L1‐PDGFRA fusion gene who had a mediastinal mass surgically excised. Pathological examination concluded to an extramedullary erythropoiesis. This case is o...

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Autores principales: Farah, Sassi, Yoldez, Houcine, Rahma, Ayadi, Mona, Mlika, Emna, Braham, Mahdi, Abdennadher, Faouzi, El Mezni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723246/
https://www.ncbi.nlm.nih.gov/pubmed/36483873
http://dx.doi.org/10.1002/ccr3.6637
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author Farah, Sassi
Yoldez, Houcine
Rahma, Ayadi
Mona, Mlika
Emna, Braham
Mahdi, Abdennadher
Faouzi, El Mezni
author_facet Farah, Sassi
Yoldez, Houcine
Rahma, Ayadi
Mona, Mlika
Emna, Braham
Mahdi, Abdennadher
Faouzi, El Mezni
author_sort Farah, Sassi
collection PubMed
description Extramedullary hematopoiesis in the posterior mediastinum is rare. Our case interested a 28‐year‐old man with a history of eosinophilia with FIP1L1‐PDGFRA fusion gene who had a mediastinal mass surgically excised. Pathological examination concluded to an extramedullary erythropoiesis. This case is original by its location and the presence of only the erythroblastic line rearrangement.
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spelling pubmed-97232462022-12-07 An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement Farah, Sassi Yoldez, Houcine Rahma, Ayadi Mona, Mlika Emna, Braham Mahdi, Abdennadher Faouzi, El Mezni Clin Case Rep Case Report Extramedullary hematopoiesis in the posterior mediastinum is rare. Our case interested a 28‐year‐old man with a history of eosinophilia with FIP1L1‐PDGFRA fusion gene who had a mediastinal mass surgically excised. Pathological examination concluded to an extramedullary erythropoiesis. This case is original by its location and the presence of only the erythroblastic line rearrangement. John Wiley and Sons Inc. 2022-12-05 /pmc/articles/PMC9723246/ /pubmed/36483873 http://dx.doi.org/10.1002/ccr3.6637 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Farah, Sassi
Yoldez, Houcine
Rahma, Ayadi
Mona, Mlika
Emna, Braham
Mahdi, Abdennadher
Faouzi, El Mezni
An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement
title An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement
title_full An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement
title_fullStr An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement
title_full_unstemmed An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement
title_short An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with FIP1L1‐PDGFRA rearrangement
title_sort intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor‐mimicking lesion in a patient with eosinophilia with fip1l1‐pdgfra rearrangement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723246/
https://www.ncbi.nlm.nih.gov/pubmed/36483873
http://dx.doi.org/10.1002/ccr3.6637
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