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Recurrent neck myxofibrosarcoma: a case report
BACKGROUND: Myxofibrosarcoma (MFS) is a rare soft tissue sarcoma with a high recurrence rate and a low risk of distant metastasis. It occurs mainly in the extremities of elderly men. Head and neck MFS is extremely rare. Surgery is the cornerstone of treatment. The role of radiotherapy (RT) and chemo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485472/ https://www.ncbi.nlm.nih.gov/pubmed/34593019 http://dx.doi.org/10.1186/s13256-021-03053-4 |
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author | Pagnoni, Chiara Improta, Luca Alloni, Rossana Mallozzi Santa Maria, Francesco Aprile, Irene Brunetti, Beniamino Greco, Carlo Vincenzi, Bruno Gronchi, Alessandro Valeri, Sergio |
author_facet | Pagnoni, Chiara Improta, Luca Alloni, Rossana Mallozzi Santa Maria, Francesco Aprile, Irene Brunetti, Beniamino Greco, Carlo Vincenzi, Bruno Gronchi, Alessandro Valeri, Sergio |
author_sort | Pagnoni, Chiara |
collection | PubMed |
description | BACKGROUND: Myxofibrosarcoma (MFS) is a rare soft tissue sarcoma with a high recurrence rate and a low risk of distant metastasis. It occurs mainly in the extremities of elderly men. Head and neck MFS is extremely rare. Surgery is the cornerstone of treatment. The role of radiotherapy (RT) and chemotherapy (CHT) on MFS is still debated. CASE PRESENTATION: A 67-year-old Caucasian man presented to our sarcoma referral center (SRC) with a history of MFS of the neck excised with microscopic positive surgical margins in a non-referral center. Staging imaging exams did not reveal distant metastasis. After a multidisciplinary discussion, preoperative RT was administered with a total dose of 50 Gy followed by wide surgical excision. Histological examination was negative for viable tumor cells. No relapse occurred during the 24-month postoperative follow-up. CONCLUSIONS: The case described suggests the importance of planned combined treatments with both RT and surgery for high-grade soft tissue sarcoma. RT seems to be promising within this specific histotype. Close follow-up is advisable in all cases. Further studies are needed to confirm if the observed efficacy of combined treatments results in a prolonged time of disease-free survival and overall survival. |
format | Online Article Text |
id | pubmed-8485472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84854722021-10-04 Recurrent neck myxofibrosarcoma: a case report Pagnoni, Chiara Improta, Luca Alloni, Rossana Mallozzi Santa Maria, Francesco Aprile, Irene Brunetti, Beniamino Greco, Carlo Vincenzi, Bruno Gronchi, Alessandro Valeri, Sergio J Med Case Rep Case Report BACKGROUND: Myxofibrosarcoma (MFS) is a rare soft tissue sarcoma with a high recurrence rate and a low risk of distant metastasis. It occurs mainly in the extremities of elderly men. Head and neck MFS is extremely rare. Surgery is the cornerstone of treatment. The role of radiotherapy (RT) and chemotherapy (CHT) on MFS is still debated. CASE PRESENTATION: A 67-year-old Caucasian man presented to our sarcoma referral center (SRC) with a history of MFS of the neck excised with microscopic positive surgical margins in a non-referral center. Staging imaging exams did not reveal distant metastasis. After a multidisciplinary discussion, preoperative RT was administered with a total dose of 50 Gy followed by wide surgical excision. Histological examination was negative for viable tumor cells. No relapse occurred during the 24-month postoperative follow-up. CONCLUSIONS: The case described suggests the importance of planned combined treatments with both RT and surgery for high-grade soft tissue sarcoma. RT seems to be promising within this specific histotype. Close follow-up is advisable in all cases. Further studies are needed to confirm if the observed efficacy of combined treatments results in a prolonged time of disease-free survival and overall survival. BioMed Central 2021-10-01 /pmc/articles/PMC8485472/ /pubmed/34593019 http://dx.doi.org/10.1186/s13256-021-03053-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Pagnoni, Chiara Improta, Luca Alloni, Rossana Mallozzi Santa Maria, Francesco Aprile, Irene Brunetti, Beniamino Greco, Carlo Vincenzi, Bruno Gronchi, Alessandro Valeri, Sergio Recurrent neck myxofibrosarcoma: a case report |
title | Recurrent neck myxofibrosarcoma: a case report |
title_full | Recurrent neck myxofibrosarcoma: a case report |
title_fullStr | Recurrent neck myxofibrosarcoma: a case report |
title_full_unstemmed | Recurrent neck myxofibrosarcoma: a case report |
title_short | Recurrent neck myxofibrosarcoma: a case report |
title_sort | recurrent neck myxofibrosarcoma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485472/ https://www.ncbi.nlm.nih.gov/pubmed/34593019 http://dx.doi.org/10.1186/s13256-021-03053-4 |
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