Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review

Epithelioid sarcoma is a rare, high-grade malignant soft tissue tumor that is often misdiagnosed. Classified as a mesenchymal malignancy, it exhibits both mesenchymal and epithelial markers. Occurrence in children under age 10 is extremely rare. This report describes the clinical course and manageme...

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Autores principales: Talbet, Joseph Hany, McGrath, Jennifer L., Manrique, Monica, Mantilla-Rivas, Esperanza, Meany, Holly J., Oh, Albert K., Rogers, Gary F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Pediatric/Craniofacial
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929078/
https://www.ncbi.nlm.nih.gov/pubmed/33680643
http://dx.doi.org/10.1097/GOX.0000000000003377
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author Talbet, Joseph Hany
McGrath, Jennifer L.
Manrique, Monica
Mantilla-Rivas, Esperanza
Meany, Holly J.
Oh, Albert K.
Rogers, Gary F.
author_facet Talbet, Joseph Hany
McGrath, Jennifer L.
Manrique, Monica
Mantilla-Rivas, Esperanza
Meany, Holly J.
Oh, Albert K.
Rogers, Gary F.
author_sort Talbet, Joseph Hany
collection PubMed
description Epithelioid sarcoma is a rare, high-grade malignant soft tissue tumor that is often misdiagnosed. Classified as a mesenchymal malignancy, it exhibits both mesenchymal and epithelial markers. Occurrence in children under age 10 is extremely rare. This report describes the clinical course and management of a 5-year-old girl who presented with epithelioid sarcoma in the distal extremity. The lesion was initially misdiagnosed and treated for over a year as a common wart.
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spelling pubmed-79290782021-03-04 Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review Talbet, Joseph Hany McGrath, Jennifer L. Manrique, Monica Mantilla-Rivas, Esperanza Meany, Holly J. Oh, Albert K. Rogers, Gary F. Plast Reconstr Surg Glob Open Pediatric/Craniofacial Epithelioid sarcoma is a rare, high-grade malignant soft tissue tumor that is often misdiagnosed. Classified as a mesenchymal malignancy, it exhibits both mesenchymal and epithelial markers. Occurrence in children under age 10 is extremely rare. This report describes the clinical course and management of a 5-year-old girl who presented with epithelioid sarcoma in the distal extremity. The lesion was initially misdiagnosed and treated for over a year as a common wart. Lippincott Williams & Wilkins 2021-02-01 /pmc/articles/PMC7929078/ /pubmed/33680643 http://dx.doi.org/10.1097/GOX.0000000000003377 Text en Copyright © 2021 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Pediatric/Craniofacial
Talbet, Joseph Hany
McGrath, Jennifer L.
Manrique, Monica
Mantilla-Rivas, Esperanza
Meany, Holly J.
Oh, Albert K.
Rogers, Gary F.
Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review
title Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review
title_full Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review
title_fullStr Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review
title_full_unstemmed Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review
title_short Epithelioid Sarcoma in a Young Child: A Case Report and Literature Review
title_sort epithelioid sarcoma in a young child: a case report and literature review
topic Pediatric/Craniofacial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929078/
https://www.ncbi.nlm.nih.gov/pubmed/33680643
http://dx.doi.org/10.1097/GOX.0000000000003377
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