Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm

Primary sarcoma of the breast is very rare and constitutes less than 1% of all breast cancers. Herein, we report a case of pleomorphic rhabdomyosarcoma (PRMS) of the right breast in a 49-year-old female patient presented with a mass (7 cm × 6.5 cm). Mammography and ultrasonography suspected a malign...

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Main Authors: Santosh Kumar Mondal, Palash Kumar Mandal, Anindya Adhikari, Bijan Basak
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:Journal of Research in Medical Sciences
Subjects:
Online Access:http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2014;volume=19;issue=12;spage=1200;epage=1202;aulast=Mondal
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spelling doaj-a0cdfac4769d4786b50c3e64418bfc522020-11-24T22:45:25ZengWolters Kluwer Medknow PublicationsJournal of Research in Medical Sciences1735-19951735-71362014-01-01191212001202Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasmSantosh Kumar MondalPalash Kumar MandalAnindya AdhikariBijan BasakPrimary sarcoma of the breast is very rare and constitutes less than 1% of all breast cancers. Herein, we report a case of pleomorphic rhabdomyosarcoma (PRMS) of the right breast in a 49-year-old female patient presented with a mass (7 cm × 6.5 cm). Mammography and ultrasonography suspected a malignant lesion and a diagnosis of poorly differentiated carcinoma was made on fine needle aspiration cytology. Modified radical mastectomy was carried out. Histopathological examination revealed a high grade stromal sarcoma with rhabdoid morphology and multinucleated tumor giant cells. The tumor cells were strongly positive for desmin, vimentin and Myo D1 focally. The tumor cells were immunonegative for cytokeratin, epithelial membrane antigen (EMA), CD34, CD45, SMA, S100, CD68 and HMB45. A final diagnosis of PRMS was rendered. Surgical margins were free and no metastasis was seen in axillary lymph nodes. Neither post-operative radiotherapy nor adjuvant chemotherapy was given and the patient has remained disease free 12 months post-operatively.http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2014;volume=19;issue=12;spage=1200;epage=1202;aulast=MondalBreastpleomorphicprimary sarcomarhabdomyosarcoma
collection DOAJ
language English
format Article
sources DOAJ
author Santosh Kumar Mondal
Palash Kumar Mandal
Anindya Adhikari
Bijan Basak
spellingShingle Santosh Kumar Mondal
Palash Kumar Mandal
Anindya Adhikari
Bijan Basak
Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm
Journal of Research in Medical Sciences
Breast
pleomorphic
primary sarcoma
rhabdomyosarcoma
author_facet Santosh Kumar Mondal
Palash Kumar Mandal
Anindya Adhikari
Bijan Basak
author_sort Santosh Kumar Mondal
title Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm
title_short Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm
title_full Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm
title_fullStr Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm
title_full_unstemmed Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm
title_sort primary pleomorphic rhabdomyosarcoma of breast: report of a rare neoplasm
publisher Wolters Kluwer Medknow Publications
series Journal of Research in Medical Sciences
issn 1735-1995
1735-7136
publishDate 2014-01-01
description Primary sarcoma of the breast is very rare and constitutes less than 1% of all breast cancers. Herein, we report a case of pleomorphic rhabdomyosarcoma (PRMS) of the right breast in a 49-year-old female patient presented with a mass (7 cm × 6.5 cm). Mammography and ultrasonography suspected a malignant lesion and a diagnosis of poorly differentiated carcinoma was made on fine needle aspiration cytology. Modified radical mastectomy was carried out. Histopathological examination revealed a high grade stromal sarcoma with rhabdoid morphology and multinucleated tumor giant cells. The tumor cells were strongly positive for desmin, vimentin and Myo D1 focally. The tumor cells were immunonegative for cytokeratin, epithelial membrane antigen (EMA), CD34, CD45, SMA, S100, CD68 and HMB45. A final diagnosis of PRMS was rendered. Surgical margins were free and no metastasis was seen in axillary lymph nodes. Neither post-operative radiotherapy nor adjuvant chemotherapy was given and the patient has remained disease free 12 months post-operatively.
topic Breast
pleomorphic
primary sarcoma
rhabdomyosarcoma
url http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2014;volume=19;issue=12;spage=1200;epage=1202;aulast=Mondal
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