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Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review

Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare, low-grade malignant soft tissue tumor. Most of the previously reported cases about this tumor were diagnosed within the soft tissues. Here, we report a unique case of MIFS of the right parotid gland in a 39-year-old Chinese male. The tumor prim...

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Autores principales: Wei, Changhong, Yang, Xuejia, Guo, Pingping, Chen, Xiaoyu, Li, Chunjun, Chen, Jun, Zhou, Sufang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163338/
https://www.ncbi.nlm.nih.gov/pubmed/35669919
http://dx.doi.org/10.3389/fmed.2022.833822
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author Wei, Changhong
Yang, Xuejia
Guo, Pingping
Chen, Xiaoyu
Li, Chunjun
Chen, Jun
Zhou, Sufang
author_facet Wei, Changhong
Yang, Xuejia
Guo, Pingping
Chen, Xiaoyu
Li, Chunjun
Chen, Jun
Zhou, Sufang
author_sort Wei, Changhong
collection PubMed
description Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare, low-grade malignant soft tissue tumor. Most of the previously reported cases about this tumor were diagnosed within the soft tissues. Here, we report a unique case of MIFS of the right parotid gland in a 39-year-old Chinese male. The tumor primarily consisted of an inflammatory area and a mucus-like area in a migratory distribution. A number of lymphocytes, neutrophils, viral-like cells with large nucleoli, and eosinophilic cytoplasm or Reed-Sternberg-like cells, as well as spindle cells and epithelial-like aberrant cells, were observed within the tumor. They were found to express Vimentin and CD10 protein and no other specific immunohistochemical markers. The various cytomorphology and immunohistochemical features of this tumor were highly consistent with MIFS found in other sites. Therefore, several leading pathologists ultimately confirmed the final diagnosis of MIFS in the right parotid gland after repeated deliberation. To our knowledge, this is the first case of MIFS occurring in the parotid gland. Thus, our study provides a novel basis for identifying the biological behavior of the tumor in MIFS and also allows us to better understand the pathology of this rare tumor.
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spelling pubmed-91633382022-06-05 Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review Wei, Changhong Yang, Xuejia Guo, Pingping Chen, Xiaoyu Li, Chunjun Chen, Jun Zhou, Sufang Front Med (Lausanne) Medicine Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare, low-grade malignant soft tissue tumor. Most of the previously reported cases about this tumor were diagnosed within the soft tissues. Here, we report a unique case of MIFS of the right parotid gland in a 39-year-old Chinese male. The tumor primarily consisted of an inflammatory area and a mucus-like area in a migratory distribution. A number of lymphocytes, neutrophils, viral-like cells with large nucleoli, and eosinophilic cytoplasm or Reed-Sternberg-like cells, as well as spindle cells and epithelial-like aberrant cells, were observed within the tumor. They were found to express Vimentin and CD10 protein and no other specific immunohistochemical markers. The various cytomorphology and immunohistochemical features of this tumor were highly consistent with MIFS found in other sites. Therefore, several leading pathologists ultimately confirmed the final diagnosis of MIFS in the right parotid gland after repeated deliberation. To our knowledge, this is the first case of MIFS occurring in the parotid gland. Thus, our study provides a novel basis for identifying the biological behavior of the tumor in MIFS and also allows us to better understand the pathology of this rare tumor. Frontiers Media S.A. 2022-05-20 /pmc/articles/PMC9163338/ /pubmed/35669919 http://dx.doi.org/10.3389/fmed.2022.833822 Text en Copyright © 2022 Wei, Yang, Guo, Chen, Li, Chen and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Wei, Changhong
Yang, Xuejia
Guo, Pingping
Chen, Xiaoyu
Li, Chunjun
Chen, Jun
Zhou, Sufang
Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review
title Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review
title_full Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review
title_fullStr Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review
title_full_unstemmed Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review
title_short Myxoinflammatory Fibroblastic Sarcoma of the Parotid Gland: First Case Report and Literature Review
title_sort myxoinflammatory fibroblastic sarcoma of the parotid gland: first case report and literature review
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163338/
https://www.ncbi.nlm.nih.gov/pubmed/35669919
http://dx.doi.org/10.3389/fmed.2022.833822
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