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Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report
BACKGROUND: Dermatomyositis is associated with malignant tumors including breast cancer, and inflammatory breast cancer is considered to have a poorer prognosis than most breast cancers. CASE PRESENTATION: A 74-year-old Asian woman, developed erythema on her face, back, and the back of her hands, 3 ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658279/ https://www.ncbi.nlm.nih.gov/pubmed/33175305 http://dx.doi.org/10.1186/s40792-020-01066-7 |
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author | Inaguma, Gaku Shimada, Akihiko Tsunoda, Junya Matsuzaki, Tomohiko Nishi, Tomohiko Seki, Hiroaki Matsumoto, Hidetoshi |
author_facet | Inaguma, Gaku Shimada, Akihiko Tsunoda, Junya Matsuzaki, Tomohiko Nishi, Tomohiko Seki, Hiroaki Matsumoto, Hidetoshi |
author_sort | Inaguma, Gaku |
collection | PubMed |
description | BACKGROUND: Dermatomyositis is associated with malignant tumors including breast cancer, and inflammatory breast cancer is considered to have a poorer prognosis than most breast cancers. CASE PRESENTATION: A 74-year-old Asian woman, developed erythema on her face, back, and the back of her hands, 3 weeks before attending our department. At the same time, she had noticed a right breast mass and redness of the skin of the breast. The clinical findings and vacuum aspiration biopsy diagnosed inflammatory breast cancer and neoadjuvant chemotherapy was performed. The mass and enlarged axillary lymph nodes had shrunk, therefore a total mastectomy was performed. The sentinel lymph node biopsy was negative. She was discharged 7 days after surgery without any complications. She has received a postoperative aromatase inhibitor and is alive without recurrence. The dermatomyositis also began to improve with the start of her chemotherapy and has not recurred since the surgery. CONCLUSIONS: Neoadjuvant chemotherapy was performed for inflammatory breast cancer with dermatomyositis, and tumor shrinkage was confirmed. A total mastectomy without axillary lymph node dissection was performed. Dermatomyositis and breast cancer have not recurred. Dermatomyositis may have been a paraneoplastic syndrome due to breast cancer. |
format | Online Article Text |
id | pubmed-7658279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-76582792020-11-16 Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report Inaguma, Gaku Shimada, Akihiko Tsunoda, Junya Matsuzaki, Tomohiko Nishi, Tomohiko Seki, Hiroaki Matsumoto, Hidetoshi Surg Case Rep Case Report BACKGROUND: Dermatomyositis is associated with malignant tumors including breast cancer, and inflammatory breast cancer is considered to have a poorer prognosis than most breast cancers. CASE PRESENTATION: A 74-year-old Asian woman, developed erythema on her face, back, and the back of her hands, 3 weeks before attending our department. At the same time, she had noticed a right breast mass and redness of the skin of the breast. The clinical findings and vacuum aspiration biopsy diagnosed inflammatory breast cancer and neoadjuvant chemotherapy was performed. The mass and enlarged axillary lymph nodes had shrunk, therefore a total mastectomy was performed. The sentinel lymph node biopsy was negative. She was discharged 7 days after surgery without any complications. She has received a postoperative aromatase inhibitor and is alive without recurrence. The dermatomyositis also began to improve with the start of her chemotherapy and has not recurred since the surgery. CONCLUSIONS: Neoadjuvant chemotherapy was performed for inflammatory breast cancer with dermatomyositis, and tumor shrinkage was confirmed. A total mastectomy without axillary lymph node dissection was performed. Dermatomyositis and breast cancer have not recurred. Dermatomyositis may have been a paraneoplastic syndrome due to breast cancer. Springer Berlin Heidelberg 2020-11-11 /pmc/articles/PMC7658279/ /pubmed/33175305 http://dx.doi.org/10.1186/s40792-020-01066-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Case Report Inaguma, Gaku Shimada, Akihiko Tsunoda, Junya Matsuzaki, Tomohiko Nishi, Tomohiko Seki, Hiroaki Matsumoto, Hidetoshi Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
title | Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
title_full | Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
title_fullStr | Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
title_full_unstemmed | Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
title_short | Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
title_sort | inflammatory breast cancer associated with amyopathic dermatomyositis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658279/ https://www.ncbi.nlm.nih.gov/pubmed/33175305 http://dx.doi.org/10.1186/s40792-020-01066-7 |
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