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The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor

The epithelioid blue nevus (EBN) is considered a cutaneous marker of the Carney complex. Sporadic EBN has been reported in patients not exhibiting the Carney complex. The EBN does not exhibit unique clinical features that help to differentiate it from other lesions and is often provisionally diagnos...

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Autores principales: Hanna, Atef, Rawal, Swati Y, Anderson, Kenneth M, Rawal, Yeshwant B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125665/
https://www.ncbi.nlm.nih.gov/pubmed/21731286
http://dx.doi.org/10.4103/0973-029X.80018
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author Hanna, Atef
Rawal, Swati Y
Anderson, Kenneth M
Rawal, Yeshwant B
author_facet Hanna, Atef
Rawal, Swati Y
Anderson, Kenneth M
Rawal, Yeshwant B
author_sort Hanna, Atef
collection PubMed
description The epithelioid blue nevus (EBN) is considered a cutaneous marker of the Carney complex. Sporadic EBN has been reported in patients not exhibiting the Carney complex. The EBN does not exhibit unique clinical features that help to differentiate it from other lesions and is often provisionally diagnosed as an acquired melanocytic nevus, or a malignant melanoma. A 52-year-old African-American female had a 3-4 mm bluish macule of the left anterior hard palate. An excisional biopsy was performed to rule out an incipient melanoma. Formalin-fixed, hematoxylin and eosin-stained sections were examined microscopically. On the basis of histopathological features, a diagnosis of EBN was rendered. We document a case of the rare EBN affecting the oral mucosa. The patient did not exhibit any features associated with the Carney complex. Two years post-operatively, there is no evidence of a recurrent tumor.
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spelling pubmed-31256652011-07-01 The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor Hanna, Atef Rawal, Swati Y Anderson, Kenneth M Rawal, Yeshwant B J Oral Maxillofac Pathol Case Report The epithelioid blue nevus (EBN) is considered a cutaneous marker of the Carney complex. Sporadic EBN has been reported in patients not exhibiting the Carney complex. The EBN does not exhibit unique clinical features that help to differentiate it from other lesions and is often provisionally diagnosed as an acquired melanocytic nevus, or a malignant melanoma. A 52-year-old African-American female had a 3-4 mm bluish macule of the left anterior hard palate. An excisional biopsy was performed to rule out an incipient melanoma. Formalin-fixed, hematoxylin and eosin-stained sections were examined microscopically. On the basis of histopathological features, a diagnosis of EBN was rendered. We document a case of the rare EBN affecting the oral mucosa. The patient did not exhibit any features associated with the Carney complex. Two years post-operatively, there is no evidence of a recurrent tumor. Medknow Publications 2011 /pmc/articles/PMC3125665/ /pubmed/21731286 http://dx.doi.org/10.4103/0973-029X.80018 Text en © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of 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
Hanna, Atef
Rawal, Swati Y
Anderson, Kenneth M
Rawal, Yeshwant B
The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor
title The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor
title_full The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor
title_fullStr The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor
title_full_unstemmed The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor
title_short The epithelioid blue nevus: A rare intraoral nevomelanocytic tumor
title_sort epithelioid blue nevus: a rare intraoral nevomelanocytic tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125665/
https://www.ncbi.nlm.nih.gov/pubmed/21731286
http://dx.doi.org/10.4103/0973-029X.80018
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