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Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives

Myxofibrosarcoma (MFS) is one of the most common adult soft tissue sarcomas, typically arising in the extremities. Histologically, MFS is classified into three grades: low, intermediate, and high. Histological grades correlate with distant metastases and tumor-associated mortality. The diagnosis of...

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Autores principales: Nishio, Jun, Nakayama, Shizuhide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572210/
https://www.ncbi.nlm.nih.gov/pubmed/37835765
http://dx.doi.org/10.3390/diagnostics13193022
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author Nishio, Jun
Nakayama, Shizuhide
author_facet Nishio, Jun
Nakayama, Shizuhide
author_sort Nishio, Jun
collection PubMed
description Myxofibrosarcoma (MFS) is one of the most common adult soft tissue sarcomas, typically arising in the extremities. Histologically, MFS is classified into three grades: low, intermediate, and high. Histological grades correlate with distant metastases and tumor-associated mortality. The diagnosis of MFS is challenging due to a lack of well-characterized immunohistochemical markers. High-grade MFS displays highly complex karyotypes with multiple copy number alterations. Recent integrated genomic studies have shown the predominance of somatic copy number aberrations. However, the molecular pathogenesis of high-grade MFS remains poorly understood. The standard treatment for localized MFS is surgical resection. The systemic treatment options for advanced disease are limited. This review provides an updated overview of the clinical and imaging features, pathogenesis, histopathology, and treatment of high-grade MFS.
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spelling pubmed-105722102023-10-14 Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives Nishio, Jun Nakayama, Shizuhide Diagnostics (Basel) Review Myxofibrosarcoma (MFS) is one of the most common adult soft tissue sarcomas, typically arising in the extremities. Histologically, MFS is classified into three grades: low, intermediate, and high. Histological grades correlate with distant metastases and tumor-associated mortality. The diagnosis of MFS is challenging due to a lack of well-characterized immunohistochemical markers. High-grade MFS displays highly complex karyotypes with multiple copy number alterations. Recent integrated genomic studies have shown the predominance of somatic copy number aberrations. However, the molecular pathogenesis of high-grade MFS remains poorly understood. The standard treatment for localized MFS is surgical resection. The systemic treatment options for advanced disease are limited. This review provides an updated overview of the clinical and imaging features, pathogenesis, histopathology, and treatment of high-grade MFS. MDPI 2023-09-22 /pmc/articles/PMC10572210/ /pubmed/37835765 http://dx.doi.org/10.3390/diagnostics13193022 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nishio, Jun
Nakayama, Shizuhide
Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
title Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
title_full Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
title_fullStr Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
title_full_unstemmed Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
title_short Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
title_sort biology and management of high-grade myxofibrosarcoma: state of the art and future perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572210/
https://www.ncbi.nlm.nih.gov/pubmed/37835765
http://dx.doi.org/10.3390/diagnostics13193022
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