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CD34 negative superficial acral fibromyxoma: A rare case report
Superficial acral fibromyxoma (SAF) is a slow growing soft tissue tumor that mainly appears in the acral areas. Here, we report a case of a SAF with distinctive immunophenotype charachteristics. An 18-year-old female was referred to our clinic with the complaint of painless subungual nodule of great...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297271/ https://www.ncbi.nlm.nih.gov/pubmed/28217473 http://dx.doi.org/10.4103/2229-5178.198776 |
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author | Robati, Reza M. Dadkhahfar, Sahar Rakhshan, Azadeh |
author_facet | Robati, Reza M. Dadkhahfar, Sahar Rakhshan, Azadeh |
author_sort | Robati, Reza M. |
collection | PubMed |
description | Superficial acral fibromyxoma (SAF) is a slow growing soft tissue tumor that mainly appears in the acral areas. Here, we report a case of a SAF with distinctive immunophenotype charachteristics. An 18-year-old female was referred to our clinic with the complaint of painless subungual nodule of great toe for a few months. The diagnosis of SAF was made according to histopathology and immunohistochemical (IHC) study, however, the IHC assessment showed positive staining with vimentin, focal reaction with smooth muscle actin, negative reaction with CD34, and positive staining pattern with CD99. These IHC findings are unusual for SAF. This reported case of SAF supports the fact that, although CD34 expression is characteristic for SAF, it is not always present. |
format | Online Article Text |
id | pubmed-5297271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52972712017-02-17 CD34 negative superficial acral fibromyxoma: A rare case report Robati, Reza M. Dadkhahfar, Sahar Rakhshan, Azadeh Indian Dermatol Online J Case Report Superficial acral fibromyxoma (SAF) is a slow growing soft tissue tumor that mainly appears in the acral areas. Here, we report a case of a SAF with distinctive immunophenotype charachteristics. An 18-year-old female was referred to our clinic with the complaint of painless subungual nodule of great toe for a few months. The diagnosis of SAF was made according to histopathology and immunohistochemical (IHC) study, however, the IHC assessment showed positive staining with vimentin, focal reaction with smooth muscle actin, negative reaction with CD34, and positive staining pattern with CD99. These IHC findings are unusual for SAF. This reported case of SAF supports the fact that, although CD34 expression is characteristic for SAF, it is not always present. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5297271/ /pubmed/28217473 http://dx.doi.org/10.4103/2229-5178.198776 Text en Copyright: © 2017 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Robati, Reza M. Dadkhahfar, Sahar Rakhshan, Azadeh CD34 negative superficial acral fibromyxoma: A rare case report |
title | CD34 negative superficial acral fibromyxoma: A rare case report |
title_full | CD34 negative superficial acral fibromyxoma: A rare case report |
title_fullStr | CD34 negative superficial acral fibromyxoma: A rare case report |
title_full_unstemmed | CD34 negative superficial acral fibromyxoma: A rare case report |
title_short | CD34 negative superficial acral fibromyxoma: A rare case report |
title_sort | cd34 negative superficial acral fibromyxoma: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297271/ https://www.ncbi.nlm.nih.gov/pubmed/28217473 http://dx.doi.org/10.4103/2229-5178.198776 |
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