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Primary breast angiosarcoma in a young woman
INTRODUCTION: Angiosarcomas of the breast are a rare subtype of sarcomas that frequently are diagnosed after radiation therapy for primary breast cancer. Primary angiosarcomas are rare entities accounting 0.05% of all malignant breast neoplasm. PRESENTATION OF CASE: We report a case of primary angio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885116/ https://www.ncbi.nlm.nih.gov/pubmed/27232295 http://dx.doi.org/10.1016/j.ijscr.2016.05.015 |
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author | Iacoponi, Sara Calleja, Jackie Hernandez, Gines Sainz de la Cuesta, Ricardo |
author_facet | Iacoponi, Sara Calleja, Jackie Hernandez, Gines Sainz de la Cuesta, Ricardo |
author_sort | Iacoponi, Sara |
collection | PubMed |
description | INTRODUCTION: Angiosarcomas of the breast are a rare subtype of sarcomas that frequently are diagnosed after radiation therapy for primary breast cancer. Primary angiosarcomas are rare entities accounting 0.05% of all malignant breast neoplasm. PRESENTATION OF CASE: We report a case of primary angiosarcoma of the breast in a 25 years woman, with no previous radiotherapy, treated with a total mastectomy followed by radio-chemotherapy. DISCUSSION: Total mastectomy appears to be the only treatment known that has proven to benefit these patients. Adjuvant treatment has not proven value up until today. The 5-year disease free survival for grade 1 tumors can be as high as 76%, and up to 15% for grade 3. CONCLUSION: Due to the rarity of these tumors there is no standard therapies approach. |
format | Online Article Text |
id | pubmed-4885116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48851162016-06-07 Primary breast angiosarcoma in a young woman Iacoponi, Sara Calleja, Jackie Hernandez, Gines Sainz de la Cuesta, Ricardo Int J Surg Case Rep Case Report INTRODUCTION: Angiosarcomas of the breast are a rare subtype of sarcomas that frequently are diagnosed after radiation therapy for primary breast cancer. Primary angiosarcomas are rare entities accounting 0.05% of all malignant breast neoplasm. PRESENTATION OF CASE: We report a case of primary angiosarcoma of the breast in a 25 years woman, with no previous radiotherapy, treated with a total mastectomy followed by radio-chemotherapy. DISCUSSION: Total mastectomy appears to be the only treatment known that has proven to benefit these patients. Adjuvant treatment has not proven value up until today. The 5-year disease free survival for grade 1 tumors can be as high as 76%, and up to 15% for grade 3. CONCLUSION: Due to the rarity of these tumors there is no standard therapies approach. Elsevier 2016-05-18 /pmc/articles/PMC4885116/ /pubmed/27232295 http://dx.doi.org/10.1016/j.ijscr.2016.05.015 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Iacoponi, Sara Calleja, Jackie Hernandez, Gines Sainz de la Cuesta, Ricardo Primary breast angiosarcoma in a young woman |
title | Primary breast angiosarcoma in a young woman |
title_full | Primary breast angiosarcoma in a young woman |
title_fullStr | Primary breast angiosarcoma in a young woman |
title_full_unstemmed | Primary breast angiosarcoma in a young woman |
title_short | Primary breast angiosarcoma in a young woman |
title_sort | primary breast angiosarcoma in a young woman |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885116/ https://www.ncbi.nlm.nih.gov/pubmed/27232295 http://dx.doi.org/10.1016/j.ijscr.2016.05.015 |
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