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Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review
BACKGROUND: Primary osteosarcoma of the breast (POB) is an extremely aggressive and heterogeneous neoplasm that originates from nonepithelial elements of the mammary gland and accounts for fewer than 1% of breast cancers and fewer than 5% of all sarcomas. CASE PRESENTATION: An 83-year-old Chinese wo...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218342/ https://www.ncbi.nlm.nih.gov/pubmed/35756647 http://dx.doi.org/10.3389/fonc.2022.875793 |
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author | Li, Shike Xue, Qingfeng Shi, Wenyu |
author_facet | Li, Shike Xue, Qingfeng Shi, Wenyu |
author_sort | Li, Shike |
collection | PubMed |
description | BACKGROUND: Primary osteosarcoma of the breast (POB) is an extremely aggressive and heterogeneous neoplasm that originates from nonepithelial elements of the mammary gland and accounts for fewer than 1% of breast cancers and fewer than 5% of all sarcomas. CASE PRESENTATION: An 83-year-old Chinese woman went to our hospital because of a palpable mass she had had for 8 months in the left breast accompanied by persistent dull pain for 10 days. This mass was initially misdiagnosed as a degenerating fibroadenoma and was graded as probably benign (BI-RADS category 3) by ultrasonography (US) and computed tomography (CT) plain scan and contrast enhancement of chest. Eight months later, it was presumed to be highly malignant and graded as BI-RADS category 4C because of its rapid growth and more calcifications by US and CT. 99mTc-MDP whole-body bone imaging showed that there was a mass-like abnormal radioactive concentration of Tc-99m outside the bone of the left chest. The lumpectomy of the left breast was indicated, and the pathological findings were POB. She succumbed to respiratory failure caused by multiple lung metastases 4 months after the operation. CONCLUSION: POB is rare, and US and CT cannot reliably distinguish the causes of calcified breast masses between benign and malignant tumors. It can be diagnosed by pathology when metaplastic carcinoma, malignant phyllodes tumor, or carcinosarcoma containing osteoid and bone is excluded. This case could help clinicians to improve the prognosis and treatment of this disease. |
format | Online Article Text |
id | pubmed-9218342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92183422022-06-24 Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review Li, Shike Xue, Qingfeng Shi, Wenyu Front Oncol Oncology BACKGROUND: Primary osteosarcoma of the breast (POB) is an extremely aggressive and heterogeneous neoplasm that originates from nonepithelial elements of the mammary gland and accounts for fewer than 1% of breast cancers and fewer than 5% of all sarcomas. CASE PRESENTATION: An 83-year-old Chinese woman went to our hospital because of a palpable mass she had had for 8 months in the left breast accompanied by persistent dull pain for 10 days. This mass was initially misdiagnosed as a degenerating fibroadenoma and was graded as probably benign (BI-RADS category 3) by ultrasonography (US) and computed tomography (CT) plain scan and contrast enhancement of chest. Eight months later, it was presumed to be highly malignant and graded as BI-RADS category 4C because of its rapid growth and more calcifications by US and CT. 99mTc-MDP whole-body bone imaging showed that there was a mass-like abnormal radioactive concentration of Tc-99m outside the bone of the left chest. The lumpectomy of the left breast was indicated, and the pathological findings were POB. She succumbed to respiratory failure caused by multiple lung metastases 4 months after the operation. CONCLUSION: POB is rare, and US and CT cannot reliably distinguish the causes of calcified breast masses between benign and malignant tumors. It can be diagnosed by pathology when metaplastic carcinoma, malignant phyllodes tumor, or carcinosarcoma containing osteoid and bone is excluded. This case could help clinicians to improve the prognosis and treatment of this disease. Frontiers Media S.A. 2022-06-09 /pmc/articles/PMC9218342/ /pubmed/35756647 http://dx.doi.org/10.3389/fonc.2022.875793 Text en Copyright © 2022 Li, Xue and Shi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Li, Shike Xue, Qingfeng Shi, Wenyu Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review |
title | Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review |
title_full | Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review |
title_fullStr | Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review |
title_full_unstemmed | Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review |
title_short | Primary Osteosarcoma of the Breast: A Rare Case Report and Literature Review |
title_sort | primary osteosarcoma of the breast: a rare case report and literature review |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218342/ https://www.ncbi.nlm.nih.gov/pubmed/35756647 http://dx.doi.org/10.3389/fonc.2022.875793 |
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