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Dendritic fibromyxolipoma: A case report

Dendritic fibromyxolipoma (DFML) is a rare variant of spindle cell lipoma. It is characterized by extensive myxoid change and the presence of stellate cells with dendritic processes. The present study reports three cases of DFML that arose from the limbs and thoracic cavity. Pathologically, the tumo...

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Autores principales: Liu, Hongyun, Hei, Shumin, Wang, Jigang, Zhang, Qiliang, Yu, Xinjuan, Chen, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690240/
https://www.ncbi.nlm.nih.gov/pubmed/33262887
http://dx.doi.org/10.3892/mco.2020.2169
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author Liu, Hongyun
Hei, Shumin
Wang, Jigang
Zhang, Qiliang
Yu, Xinjuan
Chen, Hua
author_facet Liu, Hongyun
Hei, Shumin
Wang, Jigang
Zhang, Qiliang
Yu, Xinjuan
Chen, Hua
author_sort Liu, Hongyun
collection PubMed
description Dendritic fibromyxolipoma (DFML) is a rare variant of spindle cell lipoma. It is characterized by extensive myxoid change and the presence of stellate cells with dendritic processes. The present study reports three cases of DFML that arose from the limbs and thoracic cavity. Pathologically, the tumor was composed of mature adipocytes admixing with patch spindle cells in a myxoid stroma. The cell atypia was not apparent and mitotic figures were rare. Immunohistochemistry revealed that the spindle cells were strongly positive for CD34. The three patients demonstrated no significant issues during a two-year's follow-up without evidence of recurrence and metastasis. The current study additionally reviewed all reported DFML cases in the PubMed database and Chinese journals.
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spelling pubmed-76902402020-11-30 Dendritic fibromyxolipoma: A case report Liu, Hongyun Hei, Shumin Wang, Jigang Zhang, Qiliang Yu, Xinjuan Chen, Hua Mol Clin Oncol Articles Dendritic fibromyxolipoma (DFML) is a rare variant of spindle cell lipoma. It is characterized by extensive myxoid change and the presence of stellate cells with dendritic processes. The present study reports three cases of DFML that arose from the limbs and thoracic cavity. Pathologically, the tumor was composed of mature adipocytes admixing with patch spindle cells in a myxoid stroma. The cell atypia was not apparent and mitotic figures were rare. Immunohistochemistry revealed that the spindle cells were strongly positive for CD34. The three patients demonstrated no significant issues during a two-year's follow-up without evidence of recurrence and metastasis. The current study additionally reviewed all reported DFML cases in the PubMed database and Chinese journals. D.A. Spandidos 2021-01 2020-11-12 /pmc/articles/PMC7690240/ /pubmed/33262887 http://dx.doi.org/10.3892/mco.2020.2169 Text en Copyright: © Liu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Liu, Hongyun
Hei, Shumin
Wang, Jigang
Zhang, Qiliang
Yu, Xinjuan
Chen, Hua
Dendritic fibromyxolipoma: A case report
title Dendritic fibromyxolipoma: A case report
title_full Dendritic fibromyxolipoma: A case report
title_fullStr Dendritic fibromyxolipoma: A case report
title_full_unstemmed Dendritic fibromyxolipoma: A case report
title_short Dendritic fibromyxolipoma: A case report
title_sort dendritic fibromyxolipoma: a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690240/
https://www.ncbi.nlm.nih.gov/pubmed/33262887
http://dx.doi.org/10.3892/mco.2020.2169
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AT yuxinjuan dendriticfibromyxolipomaacasereport
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