Cargando…
Rare forearm intramuscular myxoma: A case report
KEY CLINICAL MESSAGE: Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that occurs mainly in skeletal muscles which can be removed through surgery after diagnosis. ABSTRACT: Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that typically oc...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230414/ https://www.ncbi.nlm.nih.gov/pubmed/37266345 http://dx.doi.org/10.1002/ccr3.7467 |
_version_ | 1785051521901133824 |
---|---|
author | Pirmohamadi, Hosein Begloo, Mahmood Jafar Rahimi, Mohsen Akbaribazm, Mohsen |
author_facet | Pirmohamadi, Hosein Begloo, Mahmood Jafar Rahimi, Mohsen Akbaribazm, Mohsen |
author_sort | Pirmohamadi, Hosein |
collection | PubMed |
description | KEY CLINICAL MESSAGE: Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that occurs mainly in skeletal muscles which can be removed through surgery after diagnosis. ABSTRACT: Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that typically occurs in skeletal muscles. Its diagnosis is based on magnetic resonance imaging (MRI) and histopathologic evaluation of the lesion. In our report, we describe the case of a 60‐year‐old female with an IMM in the supinator muscle of the right forearm, which was confirmed by MRI and histopathologic examination. Following surgery to remove the mass, a follow‐up confirmed the patient's recovery and the absence of movement limitations in the elbow joint. |
format | Online Article Text |
id | pubmed-10230414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102304142023-06-01 Rare forearm intramuscular myxoma: A case report Pirmohamadi, Hosein Begloo, Mahmood Jafar Rahimi, Mohsen Akbaribazm, Mohsen Clin Case Rep Case Report KEY CLINICAL MESSAGE: Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that occurs mainly in skeletal muscles which can be removed through surgery after diagnosis. ABSTRACT: Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that typically occurs in skeletal muscles. Its diagnosis is based on magnetic resonance imaging (MRI) and histopathologic evaluation of the lesion. In our report, we describe the case of a 60‐year‐old female with an IMM in the supinator muscle of the right forearm, which was confirmed by MRI and histopathologic examination. Following surgery to remove the mass, a follow‐up confirmed the patient's recovery and the absence of movement limitations in the elbow joint. John Wiley and Sons Inc. 2023-05-31 /pmc/articles/PMC10230414/ /pubmed/37266345 http://dx.doi.org/10.1002/ccr3.7467 Text en © 2023 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 Pirmohamadi, Hosein Begloo, Mahmood Jafar Rahimi, Mohsen Akbaribazm, Mohsen Rare forearm intramuscular myxoma: A case report |
title | Rare forearm intramuscular myxoma: A case report |
title_full | Rare forearm intramuscular myxoma: A case report |
title_fullStr | Rare forearm intramuscular myxoma: A case report |
title_full_unstemmed | Rare forearm intramuscular myxoma: A case report |
title_short | Rare forearm intramuscular myxoma: A case report |
title_sort | rare forearm intramuscular myxoma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230414/ https://www.ncbi.nlm.nih.gov/pubmed/37266345 http://dx.doi.org/10.1002/ccr3.7467 |
work_keys_str_mv | AT pirmohamadihosein rareforearmintramuscularmyxomaacasereport AT begloomahmoodjafar rareforearmintramuscularmyxomaacasereport AT rahimimohsen rareforearmintramuscularmyxomaacasereport AT akbaribazmmohsen rareforearmintramuscularmyxomaacasereport |