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Apocrine Adenocarcinoma of the Vulva
Cutaneous vulvar carcinomas are predominantly of squamous cell carcinoma type. Primary vulvar adenocarcinomas are rare with a poorly understood histogenesis. They are classified into extramammary Paget’s disease, sweat gland carcinomas, and breast-like adenocarcinomas of the vulva. Adenocarcinomas,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804815/ https://www.ncbi.nlm.nih.gov/pubmed/24179652 http://dx.doi.org/10.4081/rt.2013.e40 |
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author | Kajal, Babita Talati, Hetal Daya, Dean Alowami, Salem |
author_facet | Kajal, Babita Talati, Hetal Daya, Dean Alowami, Salem |
author_sort | Kajal, Babita |
collection | PubMed |
description | Cutaneous vulvar carcinomas are predominantly of squamous cell carcinoma type. Primary vulvar adenocarcinomas are rare with a poorly understood histogenesis. They are classified into extramammary Paget’s disease, sweat gland carcinomas, and breast-like adenocarcinomas of the vulva. Adenocarcinomas, originating from Bartholin glands, can also present as vulvar adenocarcinoma. Rare adenocarcinomas with apocrine features have been described in the literature. The origin of these neoplasms from the native apocrine sweat glands or from anogenital mammary-like glands is still debatable. We report herein a case of a 67 year old female with a rare primary apocrine carcinoma of the vulva. |
format | Online Article Text |
id | pubmed-3804815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-38048152013-10-31 Apocrine Adenocarcinoma of the Vulva Kajal, Babita Talati, Hetal Daya, Dean Alowami, Salem Rare Tumors Case Report Cutaneous vulvar carcinomas are predominantly of squamous cell carcinoma type. Primary vulvar adenocarcinomas are rare with a poorly understood histogenesis. They are classified into extramammary Paget’s disease, sweat gland carcinomas, and breast-like adenocarcinomas of the vulva. Adenocarcinomas, originating from Bartholin glands, can also present as vulvar adenocarcinoma. Rare adenocarcinomas with apocrine features have been described in the literature. The origin of these neoplasms from the native apocrine sweat glands or from anogenital mammary-like glands is still debatable. We report herein a case of a 67 year old female with a rare primary apocrine carcinoma of the vulva. PAGEPress Publications, Pavia, Italy 2013-09-09 /pmc/articles/PMC3804815/ /pubmed/24179652 http://dx.doi.org/10.4081/rt.2013.e40 Text en ©Copyright B. Kajal et al. 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 (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kajal, Babita Talati, Hetal Daya, Dean Alowami, Salem Apocrine Adenocarcinoma of the Vulva |
title | Apocrine Adenocarcinoma of the Vulva |
title_full | Apocrine Adenocarcinoma of the Vulva |
title_fullStr | Apocrine Adenocarcinoma of the Vulva |
title_full_unstemmed | Apocrine Adenocarcinoma of the Vulva |
title_short | Apocrine Adenocarcinoma of the Vulva |
title_sort | apocrine adenocarcinoma of the vulva |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804815/ https://www.ncbi.nlm.nih.gov/pubmed/24179652 http://dx.doi.org/10.4081/rt.2013.e40 |
work_keys_str_mv | AT kajalbabita apocrineadenocarcinomaofthevulva AT talatihetal apocrineadenocarcinomaofthevulva AT dayadean apocrineadenocarcinomaofthevulva AT alowamisalem apocrineadenocarcinomaofthevulva |