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Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma

INTRODUCTION: Primary osteosarcoma of the breast is extremely rare, and an osteosarcoma arising from an intraductal papilloma is exceptional. CASE PRESENTATION: A 72-year-old Saudi Arabian woman presented with a solid, bone-containing breast mass that was diagnosed as primary osteosarcoma of the bre...

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Autores principales: Alghofaily, Khalefa Ali, Almushayqih, Musab Hamoud, Alanazi, Muhannad Faleh, Salamah, Abdullah Abdulrahman Bin, Benediktsson, Halldor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5497655/
https://www.ncbi.nlm.nih.gov/pubmed/28713607
http://dx.doi.org/10.1155/2017/5787829
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author Alghofaily, Khalefa Ali
Almushayqih, Musab Hamoud
Alanazi, Muhannad Faleh
Salamah, Abdullah Abdulrahman Bin
Benediktsson, Halldor
author_facet Alghofaily, Khalefa Ali
Almushayqih, Musab Hamoud
Alanazi, Muhannad Faleh
Salamah, Abdullah Abdulrahman Bin
Benediktsson, Halldor
author_sort Alghofaily, Khalefa Ali
collection PubMed
description INTRODUCTION: Primary osteosarcoma of the breast is extremely rare, and an osteosarcoma arising from an intraductal papilloma is exceptional. CASE PRESENTATION: A 72-year-old Saudi Arabian woman presented with a solid, bone-containing breast mass that was diagnosed as primary osteosarcoma of the breast on biopsy. She had a history of untreated intraductal papilloma. Treatment was completed with a modified mastectomy after excluding extramammary metastases. However, she subsequently developed multiple recurrent lesions at the same site. CONCLUSION: Primary osteogenic sarcomas of the breast are very rare. Although the main treatment is resection the optimal management remains uncertain and prognosis is poor.
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spelling pubmed-54976552017-07-16 Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma Alghofaily, Khalefa Ali Almushayqih, Musab Hamoud Alanazi, Muhannad Faleh Salamah, Abdullah Abdulrahman Bin Benediktsson, Halldor Case Rep Radiol Case Report INTRODUCTION: Primary osteosarcoma of the breast is extremely rare, and an osteosarcoma arising from an intraductal papilloma is exceptional. CASE PRESENTATION: A 72-year-old Saudi Arabian woman presented with a solid, bone-containing breast mass that was diagnosed as primary osteosarcoma of the breast on biopsy. She had a history of untreated intraductal papilloma. Treatment was completed with a modified mastectomy after excluding extramammary metastases. However, she subsequently developed multiple recurrent lesions at the same site. CONCLUSION: Primary osteogenic sarcomas of the breast are very rare. Although the main treatment is resection the optimal management remains uncertain and prognosis is poor. Hindawi 2017 2017-06-21 /pmc/articles/PMC5497655/ /pubmed/28713607 http://dx.doi.org/10.1155/2017/5787829 Text en Copyright © 2017 Khalefa Ali Alghofaily et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Alghofaily, Khalefa Ali
Almushayqih, Musab Hamoud
Alanazi, Muhannad Faleh
Salamah, Abdullah Abdulrahman Bin
Benediktsson, Halldor
Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma
title Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma
title_full Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma
title_fullStr Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma
title_full_unstemmed Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma
title_short Primary Osteosarcoma of the Breast Arising in an Intraductal Papilloma
title_sort primary osteosarcoma of the breast arising in an intraductal papilloma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5497655/
https://www.ncbi.nlm.nih.gov/pubmed/28713607
http://dx.doi.org/10.1155/2017/5787829
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