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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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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. |
format | Online Article Text |
id | pubmed-5203870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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