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Adenoid cystic carcinoma of the breast

Adenoid cystic carcinoma of the breast (ACC) is a rare tumor, comprising <0.1% of all breast cancers. It has a unique dual-cell pattern and is indistinguishable from ACC arising from salivary tissue. It is a low-grade tumor with favorable prognosis, and rare metastasis, with unique features. It i...

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Detalles Bibliográficos
Autores principales: Thomas, Devon N, Asarian, Armand, Xiao, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344919/
https://www.ncbi.nlm.nih.gov/pubmed/30697408
http://dx.doi.org/10.1093/jscr/rjy355
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author Thomas, Devon N
Asarian, Armand
Xiao, Philip
author_facet Thomas, Devon N
Asarian, Armand
Xiao, Philip
author_sort Thomas, Devon N
collection PubMed
description Adenoid cystic carcinoma of the breast (ACC) is a rare tumor, comprising <0.1% of all breast cancers. It has a unique dual-cell pattern and is indistinguishable from ACC arising from salivary tissue. It is a low-grade tumor with favorable prognosis, and rare metastasis, with unique features. It is more commonly seen in older women with a mean age at diagnosis of 63, with Caucasian women being at greatest risk. Most cases present as a painful, palpable mass in the outer quadrants of the breast, and must be diagnosed via core needle biopsy or surgical excisional biopsy. Although few other cancers resemble ACC it is commonly misdiagnosed. Given the rarity of this cancer, treatment guidelines have yet to be well established. Current treatment is focused around surgical resection, however, there are not specific recommendations for the extent of resection due to the lack of cases to draw from.
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spelling pubmed-63449192019-01-29 Adenoid cystic carcinoma of the breast Thomas, Devon N Asarian, Armand Xiao, Philip J Surg Case Rep Case Report Adenoid cystic carcinoma of the breast (ACC) is a rare tumor, comprising <0.1% of all breast cancers. It has a unique dual-cell pattern and is indistinguishable from ACC arising from salivary tissue. It is a low-grade tumor with favorable prognosis, and rare metastasis, with unique features. It is more commonly seen in older women with a mean age at diagnosis of 63, with Caucasian women being at greatest risk. Most cases present as a painful, palpable mass in the outer quadrants of the breast, and must be diagnosed via core needle biopsy or surgical excisional biopsy. Although few other cancers resemble ACC it is commonly misdiagnosed. Given the rarity of this cancer, treatment guidelines have yet to be well established. Current treatment is focused around surgical resection, however, there are not specific recommendations for the extent of resection due to the lack of cases to draw from. Oxford University Press 2019-01-24 /pmc/articles/PMC6344919/ /pubmed/30697408 http://dx.doi.org/10.1093/jscr/rjy355 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2019. 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 (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Thomas, Devon N
Asarian, Armand
Xiao, Philip
Adenoid cystic carcinoma of the breast
title Adenoid cystic carcinoma of the breast
title_full Adenoid cystic carcinoma of the breast
title_fullStr Adenoid cystic carcinoma of the breast
title_full_unstemmed Adenoid cystic carcinoma of the breast
title_short Adenoid cystic carcinoma of the breast
title_sort adenoid cystic carcinoma of the breast
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344919/
https://www.ncbi.nlm.nih.gov/pubmed/30697408
http://dx.doi.org/10.1093/jscr/rjy355
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