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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...

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Autores principales: Robati, Reza M., Dadkhahfar, Sahar, Rakhshan, Azadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
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.
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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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