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Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review

BACKGROUND: Myxofibrosarcoma (MFS), especially radiation-Induced MFS (RIMFS) in the head and neck, is an extremely rare malignant fibroblastic tumor. The diagnosis and treatment of MFS remain great challenges. In the present study, we presented one case of RIMFS. Combined with previous literature, t...

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Autores principales: Zhang, Bin, Bai, Miao, Tian, Runfa, Hao, Shuyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620227/
https://www.ncbi.nlm.nih.gov/pubmed/34823603
http://dx.doi.org/10.1186/s41016-021-00267-9
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author Zhang, Bin
Bai, Miao
Tian, Runfa
Hao, Shuyu
author_facet Zhang, Bin
Bai, Miao
Tian, Runfa
Hao, Shuyu
author_sort Zhang, Bin
collection PubMed
description BACKGROUND: Myxofibrosarcoma (MFS), especially radiation-Induced MFS (RIMFS) in the head and neck, is an extremely rare malignant fibroblastic tumor. The diagnosis and treatment of MFS remain great challenges. In the present study, we presented one case of RIMFS. Combined with previous literature, the clinical features, essentials of diagnosis, and treatment modalities of MFS in the head and neck were reviewed to better understand this rare entity. CASE PRESENTATION: We reported a case of RIMFS under the left occipital scalp in a 20-year-old girl with a history of medulloblastoma surgery and radiotherapy in 2006. A total tumor resection was performed with preservation of the overlying scalp the underlying bone, and no adjuvant therapy was administered after the first operation. The postoperative pathological diagnosis was high-grade MFS. The tumor relapsed 6 months later, and then, a planned extensive resection with negative surgical margins was carried out, followed by radiotherapy. No relapse occurred in a 12-month postoperative follow-up. CONCLUSIONS: Planned gross total resection (GTR) with negative margins is the reasonable choice and footstone of other treatments for MFS. Ill-defined infiltrated borders and the complicated structures make it a great trouble to achieve total resection of MFS in the head and neck, so adjuvant radiotherapy and chemotherapy seem more necessary for these lesions.
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spelling pubmed-86202272021-11-29 Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review Zhang, Bin Bai, Miao Tian, Runfa Hao, Shuyu Chin Neurosurg J Case Report BACKGROUND: Myxofibrosarcoma (MFS), especially radiation-Induced MFS (RIMFS) in the head and neck, is an extremely rare malignant fibroblastic tumor. The diagnosis and treatment of MFS remain great challenges. In the present study, we presented one case of RIMFS. Combined with previous literature, the clinical features, essentials of diagnosis, and treatment modalities of MFS in the head and neck were reviewed to better understand this rare entity. CASE PRESENTATION: We reported a case of RIMFS under the left occipital scalp in a 20-year-old girl with a history of medulloblastoma surgery and radiotherapy in 2006. A total tumor resection was performed with preservation of the overlying scalp the underlying bone, and no adjuvant therapy was administered after the first operation. The postoperative pathological diagnosis was high-grade MFS. The tumor relapsed 6 months later, and then, a planned extensive resection with negative surgical margins was carried out, followed by radiotherapy. No relapse occurred in a 12-month postoperative follow-up. CONCLUSIONS: Planned gross total resection (GTR) with negative margins is the reasonable choice and footstone of other treatments for MFS. Ill-defined infiltrated borders and the complicated structures make it a great trouble to achieve total resection of MFS in the head and neck, so adjuvant radiotherapy and chemotherapy seem more necessary for these lesions. BioMed Central 2021-11-26 /pmc/articles/PMC8620227/ /pubmed/34823603 http://dx.doi.org/10.1186/s41016-021-00267-9 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
Zhang, Bin
Bai, Miao
Tian, Runfa
Hao, Shuyu
Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
title Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
title_full Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
title_fullStr Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
title_full_unstemmed Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
title_short Idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
title_sort idiopathic and radiation-induced myxofibrosarcoma in the head and neck—case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620227/
https://www.ncbi.nlm.nih.gov/pubmed/34823603
http://dx.doi.org/10.1186/s41016-021-00267-9
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