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Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature

Dendritic fibromyxolipoma is a rare and distinctive soft tissue neoplasm that is considered by many authors as a variant of spindle cell lipoma and characterized by the presence of dendritic cytoplasmic processes, plexiform vascular pattern, and keloidal collagen. It has never been reported in the l...

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Autores principales: AlAbdulsalam, Abdulrahim, Arafah, Maha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203870/
https://www.ncbi.nlm.nih.gov/pubmed/28078157
http://dx.doi.org/10.1155/2016/7289017
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author AlAbdulsalam, Abdulrahim
Arafah, Maha
author_facet AlAbdulsalam, Abdulrahim
Arafah, Maha
author_sort AlAbdulsalam, Abdulrahim
collection PubMed
description Dendritic fibromyxolipoma is a rare and distinctive soft tissue neoplasm that is considered by many authors as a variant of spindle cell lipoma and characterized by the presence of dendritic cytoplasmic processes, plexiform vascular pattern, and keloidal collagen. It has never been reported in the larynx and hypopharynx. Its rarity and the potential to mistake it as a more clinically aggressive myxoid soft tissue neoplasm highlight the importance of its recognition. Here, a case of a dendritic fibromyxolipoma of the pyriform sinus in a 38-year-old male who presented with dysphagia, change of voice, and stridor is reported. A review of the literature, including histopathologic features and differential diagnosis, is also included.
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spelling pubmed-52038702017-01-11 Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature AlAbdulsalam, Abdulrahim Arafah, Maha Case Rep Pathol Case Report Dendritic fibromyxolipoma is a rare and distinctive soft tissue neoplasm that is considered by many authors as a variant of spindle cell lipoma and characterized by the presence of dendritic cytoplasmic processes, plexiform vascular pattern, and keloidal collagen. It has never been reported in the larynx and hypopharynx. Its rarity and the potential to mistake it as a more clinically aggressive myxoid soft tissue neoplasm highlight the importance of its recognition. Here, a case of a dendritic fibromyxolipoma of the pyriform sinus in a 38-year-old male who presented with dysphagia, change of voice, and stridor is reported. A review of the literature, including histopathologic features and differential diagnosis, is also included. Hindawi Publishing Corporation 2016 2016-12-18 /pmc/articles/PMC5203870/ /pubmed/28078157 http://dx.doi.org/10.1155/2016/7289017 Text en Copyright © 2016 A. AlAbdulsalam and M. Arafah. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
AlAbdulsalam, Abdulrahim
Arafah, Maha
Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature
title Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature
title_full Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature
title_fullStr Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature
title_full_unstemmed Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature
title_short Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature
title_sort dendritic fibromyxolipoma of the pyriform sinus: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203870/
https://www.ncbi.nlm.nih.gov/pubmed/28078157
http://dx.doi.org/10.1155/2016/7289017
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