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Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature
BACKGROUND: Although myxofibrosarcoma (MFS) is the most common mesenchymal tumor, occurrence in the orbit is extremely rare. A characteristic clinical feature of MFS is its propensity for local recurrence (LR). Still, none of published literature has described the entire clinical course of multiple...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336468/ https://www.ncbi.nlm.nih.gov/pubmed/32631312 http://dx.doi.org/10.1186/s12886-020-01458-1 |
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author | Du, Baixue He, Xin Wang, Yujiao He, Weimin |
author_facet | Du, Baixue He, Xin Wang, Yujiao He, Weimin |
author_sort | Du, Baixue |
collection | PubMed |
description | BACKGROUND: Although myxofibrosarcoma (MFS) is the most common mesenchymal tumor, occurrence in the orbit is extremely rare. A characteristic clinical feature of MFS is its propensity for local recurrence (LR). Still, none of published literature has described the entire clinical course of multiple recurrences of MFS in the orbit. Here we present an unusual case in which a patient with multiple recurrences of MFS in the orbit followed-up for 5 years. We describe its clinical-pathological correlation, treatment, and prognosis. CASE PRESENTATION: A 70-year-old woman sought treatment for a year history of right upper eyelid swelling in May 2014. Since then, she underwent three surgical procedures in the right orbit in the same region (in 2014, 2016, and 2017). The pathology analysis of the three surgical tissue samples was consistent with myxofibrosarcoma, characterized by spindle-shaped cells and variably myxoid stroma. In the 2 years follow-up after the third surgery, there was no evidence of tumor recurrence. CONCLUSION: Myxofibrosarcoma of the orbit is extremely rare. Since few reports are available in the literature, the diagnosis and management of the orbit myxofibrosarcoma is still a challenge to ophthalmologists. Histopathology is highly valuable in the diagnosis. As a clinical characteristic, the lesions have a high risk of local recurrence; therefore, aggressive resection and careful postoperative follow-up are paramount. |
format | Online Article Text |
id | pubmed-7336468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73364682020-07-08 Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature Du, Baixue He, Xin Wang, Yujiao He, Weimin BMC Ophthalmol Case Report BACKGROUND: Although myxofibrosarcoma (MFS) is the most common mesenchymal tumor, occurrence in the orbit is extremely rare. A characteristic clinical feature of MFS is its propensity for local recurrence (LR). Still, none of published literature has described the entire clinical course of multiple recurrences of MFS in the orbit. Here we present an unusual case in which a patient with multiple recurrences of MFS in the orbit followed-up for 5 years. We describe its clinical-pathological correlation, treatment, and prognosis. CASE PRESENTATION: A 70-year-old woman sought treatment for a year history of right upper eyelid swelling in May 2014. Since then, she underwent three surgical procedures in the right orbit in the same region (in 2014, 2016, and 2017). The pathology analysis of the three surgical tissue samples was consistent with myxofibrosarcoma, characterized by spindle-shaped cells and variably myxoid stroma. In the 2 years follow-up after the third surgery, there was no evidence of tumor recurrence. CONCLUSION: Myxofibrosarcoma of the orbit is extremely rare. Since few reports are available in the literature, the diagnosis and management of the orbit myxofibrosarcoma is still a challenge to ophthalmologists. Histopathology is highly valuable in the diagnosis. As a clinical characteristic, the lesions have a high risk of local recurrence; therefore, aggressive resection and careful postoperative follow-up are paramount. BioMed Central 2020-07-06 /pmc/articles/PMC7336468/ /pubmed/32631312 http://dx.doi.org/10.1186/s12886-020-01458-1 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Du, Baixue He, Xin Wang, Yujiao He, Weimin Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
title | Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
title_full | Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
title_fullStr | Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
title_full_unstemmed | Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
title_short | Multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
title_sort | multiple recurrent myxofibrosarcoma of the orbit: case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336468/ https://www.ncbi.nlm.nih.gov/pubmed/32631312 http://dx.doi.org/10.1186/s12886-020-01458-1 |
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