Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*

Neurothekeoma is an uncommon, benign neoplasm presenting in young adults, primarily on the head and neck. It was initially related to nerve sheath myxoma but with the advent of immunohistochemistry, new insights into its cellular differentiation and origin have emerged, unlinking Neurothekeoma and n...

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Main Authors: Navarrete-Dechent, Cristián, Curi-Tuma, Maximiliano, Marín, Celeste, González, Sergio, Sandoval-Osses, Mauricio
Format: Online
Language:English
Published: Sociedade Brasileira de Dermatologia 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540536/
id pubmed-4540536
recordtype oai_dc
spelling pubmed-45405362015-08-20 Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma* Navarrete-Dechent, Cristián Curi-Tuma, Maximiliano Marín, Celeste González, Sergio Sandoval-Osses, Mauricio Case Report Neurothekeoma is an uncommon, benign neoplasm presenting in young adults, primarily on the head and neck. It was initially related to nerve sheath myxoma but with the advent of immunohistochemistry, new insights into its cellular differentiation and origin have emerged, unlinking Neurothekeoma and nerve sheath myxoma. Herein we describe a 19-year-old male who had had a frontal, fl esh-colored, asymptomatic papule for 2 years. Histology showed a dermal fusocellular-spindle cell tumor, including an eosinophilic cytoplasm with mild cellular pleomorphism and moderately dense fi brous stroma. IHQ was positive for CD10 and negative for S100 and Claudin-1. These fi ndings were compatible with cellular Neurothekeoma. The lesion was completely extirpated and at the 6-month follow-up, the patient was asymptomatic and had experienced no recurrences. Sociedade Brasileira de Dermatologia 2015 /pmc/articles/PMC4540536/ /pubmed/26312702 http://dx.doi.org/10.1590/abd1806-4841.20153402 Text en © 2015 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Navarrete-Dechent, Cristián
Curi-Tuma, Maximiliano
Marín, Celeste
González, Sergio
Sandoval-Osses, Mauricio
spellingShingle Navarrete-Dechent, Cristián
Curi-Tuma, Maximiliano
Marín, Celeste
González, Sergio
Sandoval-Osses, Mauricio
Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
author_facet Navarrete-Dechent, Cristián
Curi-Tuma, Maximiliano
Marín, Celeste
González, Sergio
Sandoval-Osses, Mauricio
author_sort Navarrete-Dechent, Cristián
title Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
title_short Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
title_full Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
title_fullStr Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
title_full_unstemmed Cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
title_sort cellular neurothekeoma: case report and its (un) relation with nerve sheath myxoma*
description Neurothekeoma is an uncommon, benign neoplasm presenting in young adults, primarily on the head and neck. It was initially related to nerve sheath myxoma but with the advent of immunohistochemistry, new insights into its cellular differentiation and origin have emerged, unlinking Neurothekeoma and nerve sheath myxoma. Herein we describe a 19-year-old male who had had a frontal, fl esh-colored, asymptomatic papule for 2 years. Histology showed a dermal fusocellular-spindle cell tumor, including an eosinophilic cytoplasm with mild cellular pleomorphism and moderately dense fi brous stroma. IHQ was positive for CD10 and negative for S100 and Claudin-1. These fi ndings were compatible with cellular Neurothekeoma. The lesion was completely extirpated and at the 6-month follow-up, the patient was asymptomatic and had experienced no recurrences.
publisher Sociedade Brasileira de Dermatologia
publishDate 2015
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540536/
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