Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case
Sarcomas of the breast constitute less than 1% of all malignant breast tumors and primary rhabdomyosarcoma (RMS) is a very rare entity with limited case reports in the literature. RMS is common in children and adolescents and rare in adults. Primary RMS arising from the breast is exceedingly rare in...
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Hindawi Limited
2019-01-01
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Series: | Case Reports in Pathology |
Online Access: | http://dx.doi.org/10.1155/2019/6098747 |
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doaj-5e3f418d7f3844a59ec757d06f9377722020-11-25T01:36:55ZengHindawi LimitedCase Reports in Pathology2090-67812090-679X2019-01-01201910.1155/2019/60987476098747Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare CaseHelen J. Trihia0Natasa Novkovic1Ioannis Provatas2Anastasios Mavrogiorgis3Evangelos Lianos4Department of Pathology, Metaxas Memorial Cancer Hospital, Piraeus, GreeceDepartment of Pathology, Metaxas Memorial Cancer Hospital, Piraeus, GreeceDepartment of Pathology, Metaxas Memorial Cancer Hospital, Piraeus, GreeceDepartment of Pathology, Vostanio Hospital, Mytilini, GreeceDepartment of Medical Oncology, Metaxas Memorial Cancer Hospital, Piraeus, GreeceSarcomas of the breast constitute less than 1% of all malignant breast tumors and primary rhabdomyosarcoma (RMS) is a very rare entity with limited case reports in the literature. RMS is common in children and adolescents and rare in adults. Primary RMS arising from the breast is exceedingly rare in adults. We report a case of a primary RMS of the breast in a 60-year-old woman, who presented in an early stage, mimicking invasive ductal carcinoma clinically and is in complete remission after three years of diagnosis and one year of treatment.http://dx.doi.org/10.1155/2019/6098747 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Helen J. Trihia Natasa Novkovic Ioannis Provatas Anastasios Mavrogiorgis Evangelos Lianos |
spellingShingle |
Helen J. Trihia Natasa Novkovic Ioannis Provatas Anastasios Mavrogiorgis Evangelos Lianos Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case Case Reports in Pathology |
author_facet |
Helen J. Trihia Natasa Novkovic Ioannis Provatas Anastasios Mavrogiorgis Evangelos Lianos |
author_sort |
Helen J. Trihia |
title |
Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case |
title_short |
Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case |
title_full |
Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case |
title_fullStr |
Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case |
title_full_unstemmed |
Primary Alveolar Rhabdomyosarcoma of the Breast in an Adult: An Extremely Rare Case |
title_sort |
primary alveolar rhabdomyosarcoma of the breast in an adult: an extremely rare case |
publisher |
Hindawi Limited |
series |
Case Reports in Pathology |
issn |
2090-6781 2090-679X |
publishDate |
2019-01-01 |
description |
Sarcomas of the breast constitute less than 1% of all malignant breast tumors and primary rhabdomyosarcoma (RMS) is a very rare entity with limited case reports in the literature. RMS is common in children and adolescents and rare in adults. Primary RMS arising from the breast is exceedingly rare in adults. We report a case of a primary RMS of the breast in a 60-year-old woman, who presented in an early stage, mimicking invasive ductal carcinoma clinically and is in complete remission after three years of diagnosis and one year of treatment. |
url |
http://dx.doi.org/10.1155/2019/6098747 |
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AT helenjtrihia primaryalveolarrhabdomyosarcomaofthebreastinanadultanextremelyrarecase AT natasanovkovic primaryalveolarrhabdomyosarcomaofthebreastinanadultanextremelyrarecase AT ioannisprovatas primaryalveolarrhabdomyosarcomaofthebreastinanadultanextremelyrarecase AT anastasiosmavrogiorgis primaryalveolarrhabdomyosarcomaofthebreastinanadultanextremelyrarecase AT evangeloslianos primaryalveolarrhabdomyosarcomaofthebreastinanadultanextremelyrarecase |
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