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Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth
Rhabdomyosarcoma is a malignant tumor of the soft tissues which preferentially affects the pediatric population. Neonatal rhabdomyosarcoma is rare, and much of the published literature concerning this entity consists of isolated case reports and small case series. Recent work involving the classific...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091335/ https://www.ncbi.nlm.nih.gov/pubmed/30155334 http://dx.doi.org/10.1155/2018/1243436 |
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author | Waldman, Leah E. Williamson, Alex K. Amodio, John B. Collins, Lee |
author_facet | Waldman, Leah E. Williamson, Alex K. Amodio, John B. Collins, Lee |
author_sort | Waldman, Leah E. |
collection | PubMed |
description | Rhabdomyosarcoma is a malignant tumor of the soft tissues which preferentially affects the pediatric population. Neonatal rhabdomyosarcoma is rare, and much of the published literature concerning this entity consists of isolated case reports and small case series. Recent work involving the classification of rhabdomyosarcoma has helped to delineate prognostic information based on gene rearrangements. Here, we present a case of congenital rhabdomyosarcoma seen in utero which manifested as a neck mass at birth and was found to harbor a favorable gene fusion. |
format | Online Article Text |
id | pubmed-6091335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60913352018-08-28 Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth Waldman, Leah E. Williamson, Alex K. Amodio, John B. Collins, Lee Case Rep Pediatr Case Report Rhabdomyosarcoma is a malignant tumor of the soft tissues which preferentially affects the pediatric population. Neonatal rhabdomyosarcoma is rare, and much of the published literature concerning this entity consists of isolated case reports and small case series. Recent work involving the classification of rhabdomyosarcoma has helped to delineate prognostic information based on gene rearrangements. Here, we present a case of congenital rhabdomyosarcoma seen in utero which manifested as a neck mass at birth and was found to harbor a favorable gene fusion. Hindawi 2018-07-30 /pmc/articles/PMC6091335/ /pubmed/30155334 http://dx.doi.org/10.1155/2018/1243436 Text en Copyright © 2018 Leah E. Waldman et al. http://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 Waldman, Leah E. Williamson, Alex K. Amodio, John B. Collins, Lee Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth |
title | Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth |
title_full | Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth |
title_fullStr | Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth |
title_full_unstemmed | Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth |
title_short | Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth |
title_sort | congenital rhabdomyosarcoma presenting as a neck mass at birth |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091335/ https://www.ncbi.nlm.nih.gov/pubmed/30155334 http://dx.doi.org/10.1155/2018/1243436 |
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