Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis

Epithelioid angiosarcoma (EA) is a subtype of angiosarcoma which is a rare tumor of endothelial origin. Here, we report a case of 15-year-old boy who presented with soft tissue mass lesion in the parotid region mimicking as a benign parotid tumor. Cytology was suggestive of inflammatory swelling. Pa...

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Autores principales: Srivastava, Anitya, Nagpal, Ruchi, Dhingra, Harshi, Baliyan, Asif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iuliu Hatieganu University of Medicine and Pharmacy 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177093/
https://www.ncbi.nlm.nih.gov/pubmed/35720232
http://dx.doi.org/10.15386/mpr-1751
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author Srivastava, Anitya
Nagpal, Ruchi
Dhingra, Harshi
Baliyan, Asif
author_facet Srivastava, Anitya
Nagpal, Ruchi
Dhingra, Harshi
Baliyan, Asif
author_sort Srivastava, Anitya
collection PubMed
description Epithelioid angiosarcoma (EA) is a subtype of angiosarcoma which is a rare tumor of endothelial origin. Here, we report a case of 15-year-old boy who presented with soft tissue mass lesion in the parotid region mimicking as a benign parotid tumor. Cytology was suggestive of inflammatory swelling. Patient underwent superficial parotidectomy along with the wide excision of the swelling. On histopathology, it was diagnosed as EA. To the best of our knowledge this is the first case report of epithelioid angiosarcoma of the masseter.
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spelling pubmed-91770932022-06-17 Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis Srivastava, Anitya Nagpal, Ruchi Dhingra, Harshi Baliyan, Asif Med Pharm Rep Case Report Epithelioid angiosarcoma (EA) is a subtype of angiosarcoma which is a rare tumor of endothelial origin. Here, we report a case of 15-year-old boy who presented with soft tissue mass lesion in the parotid region mimicking as a benign parotid tumor. Cytology was suggestive of inflammatory swelling. Patient underwent superficial parotidectomy along with the wide excision of the swelling. On histopathology, it was diagnosed as EA. To the best of our knowledge this is the first case report of epithelioid angiosarcoma of the masseter. Iuliu Hatieganu University of Medicine and Pharmacy 2022-01 2022-01-31 /pmc/articles/PMC9177093/ /pubmed/35720232 http://dx.doi.org/10.15386/mpr-1751 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
spellingShingle Case Report
Srivastava, Anitya
Nagpal, Ruchi
Dhingra, Harshi
Baliyan, Asif
Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
title Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
title_full Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
title_fullStr Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
title_full_unstemmed Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
title_short Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
title_sort epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177093/
https://www.ncbi.nlm.nih.gov/pubmed/35720232
http://dx.doi.org/10.15386/mpr-1751
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AT baliyanasif epithelioidangiosarcomaofthemassetermusclearareclinicopathologicaldiagnosis

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