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Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report

Breast fibromatosis is a benign fibroblastic proliferation accounting for less than 0.2% of breast tumors. It presents sporadically or as a manifestation of familial adenomatous polyposis (FAP). Fibromatosis in FAP may develop in patients with adenomatous polyposis coli (APC) gene mutations at any l...

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Autores principales: Silva, Sara, Lage, Pedro, Cabral, Francisco, Alves, Rui, Catarino, Ana, Félix, Ana, André, Saudade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036415/
https://www.ncbi.nlm.nih.gov/pubmed/30008823
http://dx.doi.org/10.3892/ol.2018.8853
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author Silva, Sara
Lage, Pedro
Cabral, Francisco
Alves, Rui
Catarino, Ana
Félix, Ana
André, Saudade
author_facet Silva, Sara
Lage, Pedro
Cabral, Francisco
Alves, Rui
Catarino, Ana
Félix, Ana
André, Saudade
author_sort Silva, Sara
collection PubMed
description Breast fibromatosis is a benign fibroblastic proliferation accounting for less than 0.2% of breast tumors. It presents sporadically or as a manifestation of familial adenomatous polyposis (FAP). Fibromatosis in FAP may develop in patients with adenomatous polyposis coli (APC) gene mutations at any location through the gene. Notably, there is an increased risk if mutation is downstream codon 1400. The present case report described a 33-year-old woman with recurrent bilateral breast fibromatosis after breast implants in a context of classic FAP. APC mutation (codon-935) was detected at the age of 16. In the same year, a thyroidectomy for a cribriform-morular papillary thyroid carcinoma (pT1) was performed. Seven years later, a prophylactic total colectomy with >100 adenomas without invasive carcinoma was performed and the patient was kept under surveillance. At the age of 30 years old, she underwent breast silicone implantation for cosmetic reasons. One year later, bilateral breast tumors were diagnosed in core biopsy as fibromatosis (nuclear β-catenin+, estrogen receptors-). After no success with medical treatment with tamoxifen, bilateral mastectomy was performed. The patient relapsed one year later and a fibromatosis lesion in the right thoracic wall was excised again. The patient demonstrated no signs of relapse 24 months after the surgery. This rare case illustrates that the increased risk of developing fibromatosis in patients with FAP, even in the classic form, should be considered before deciding to place breast implants.
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spelling pubmed-60364152018-07-15 Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report Silva, Sara Lage, Pedro Cabral, Francisco Alves, Rui Catarino, Ana Félix, Ana André, Saudade Oncol Lett Articles Breast fibromatosis is a benign fibroblastic proliferation accounting for less than 0.2% of breast tumors. It presents sporadically or as a manifestation of familial adenomatous polyposis (FAP). Fibromatosis in FAP may develop in patients with adenomatous polyposis coli (APC) gene mutations at any location through the gene. Notably, there is an increased risk if mutation is downstream codon 1400. The present case report described a 33-year-old woman with recurrent bilateral breast fibromatosis after breast implants in a context of classic FAP. APC mutation (codon-935) was detected at the age of 16. In the same year, a thyroidectomy for a cribriform-morular papillary thyroid carcinoma (pT1) was performed. Seven years later, a prophylactic total colectomy with >100 adenomas without invasive carcinoma was performed and the patient was kept under surveillance. At the age of 30 years old, she underwent breast silicone implantation for cosmetic reasons. One year later, bilateral breast tumors were diagnosed in core biopsy as fibromatosis (nuclear β-catenin+, estrogen receptors-). After no success with medical treatment with tamoxifen, bilateral mastectomy was performed. The patient relapsed one year later and a fibromatosis lesion in the right thoracic wall was excised again. The patient demonstrated no signs of relapse 24 months after the surgery. This rare case illustrates that the increased risk of developing fibromatosis in patients with FAP, even in the classic form, should be considered before deciding to place breast implants. D.A. Spandidos 2018-08 2018-05-31 /pmc/articles/PMC6036415/ /pubmed/30008823 http://dx.doi.org/10.3892/ol.2018.8853 Text en Copyright: © Silva et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Silva, Sara
Lage, Pedro
Cabral, Francisco
Alves, Rui
Catarino, Ana
Félix, Ana
André, Saudade
Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report
title Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report
title_full Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report
title_fullStr Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report
title_full_unstemmed Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report
title_short Bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: A case report
title_sort bilateral breast fibromatosis after silicone prosthetics in a patient with classic familial adenomatous polyposis: a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036415/
https://www.ncbi.nlm.nih.gov/pubmed/30008823
http://dx.doi.org/10.3892/ol.2018.8853
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