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Case for diagnosis
Granular cell tumor is a rare benign neoplasm of neural origin. We report the case of a female patient, 27 years old presenting a brown-red nodule in the right arm, which pathological examination showed to be formed by polygonal cells with eosinophilic granular cytoplasm and immunohistochemistry pos...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900361/ https://www.ncbi.nlm.nih.gov/pubmed/24474119 http://dx.doi.org/10.1590/abd1806-4841.20132772 |
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author | Lage, Thaiane Lima de Miranda, Mario Fernando Ribeiro Bittencourt, Maraya de Jesus Semblano Dias, Carolina Moraes de Parijós, Amanda Magno Raiol, Theisla Kely Azevedo |
author_facet | Lage, Thaiane Lima de Miranda, Mario Fernando Ribeiro Bittencourt, Maraya de Jesus Semblano Dias, Carolina Moraes de Parijós, Amanda Magno Raiol, Theisla Kely Azevedo |
author_sort | Lage, Thaiane Lima |
collection | PubMed |
description | Granular cell tumor is a rare benign neoplasm of neural origin. We report the case of a female patient, 27 years old presenting a brown-red nodule in the right arm, which pathological examination showed to be formed by polygonal cells with eosinophilic granular cytoplasm and immunohistochemistry positive for S100 protein and CD68. Granular cell tumor is usually solitary and in half the cases located in the head and neck areas, 30% of these in the tongue. It is most frequent between the third and fifth decades of life in women and people of African-American ethnicity. Its origination is controversial, including the possible origins in muscle, fibroblasts, neural crest, neural sheath or histiocytes. The positivity for S-100 and CD68 suggest the neural origin. |
format | Online Article Text |
id | pubmed-3900361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-39003612014-01-29 Case for diagnosis Lage, Thaiane Lima de Miranda, Mario Fernando Ribeiro Bittencourt, Maraya de Jesus Semblano Dias, Carolina Moraes de Parijós, Amanda Magno Raiol, Theisla Kely Azevedo An Bras Dermatol What Is Your Diagnosis? Granular cell tumor is a rare benign neoplasm of neural origin. We report the case of a female patient, 27 years old presenting a brown-red nodule in the right arm, which pathological examination showed to be formed by polygonal cells with eosinophilic granular cytoplasm and immunohistochemistry positive for S100 protein and CD68. Granular cell tumor is usually solitary and in half the cases located in the head and neck areas, 30% of these in the tongue. It is most frequent between the third and fifth decades of life in women and people of African-American ethnicity. Its origination is controversial, including the possible origins in muscle, fibroblasts, neural crest, neural sheath or histiocytes. The positivity for S-100 and CD68 suggest the neural origin. Sociedade Brasileira de Dermatologia 2013 /pmc/articles/PMC3900361/ /pubmed/24474119 http://dx.doi.org/10.1590/abd1806-4841.20132772 Text en http://creativecommons.org/licenses/by-nc/3.0/ 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. |
spellingShingle | What Is Your Diagnosis? Lage, Thaiane Lima de Miranda, Mario Fernando Ribeiro Bittencourt, Maraya de Jesus Semblano Dias, Carolina Moraes de Parijós, Amanda Magno Raiol, Theisla Kely Azevedo Case for diagnosis |
title | Case for diagnosis
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title_full | Case for diagnosis
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title_fullStr | Case for diagnosis
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title_full_unstemmed | Case for diagnosis
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title_short | Case for diagnosis
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title_sort | case for diagnosis |
topic | What Is Your Diagnosis? |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900361/ https://www.ncbi.nlm.nih.gov/pubmed/24474119 http://dx.doi.org/10.1590/abd1806-4841.20132772 |
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