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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,...

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Detalles Bibliográficos
Autores principales: Kajal, Babita, Talati, Hetal, Daya, Dean, Alowami, Salem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2013
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.
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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
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