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Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report
Rhabdomyosarcoma (RMS) is a soft tissue sarcoma that histologically resembles embryonic skeletal muscle. It can occur anywhere in the body, including tissues devoid of skeletal muscles. RMS is a common malignancy in children, and it accounts for ˃50% of all soft tissue sarcomas in children. Embryona...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409587/ https://www.ncbi.nlm.nih.gov/pubmed/37560601 http://dx.doi.org/10.1093/jscr/rjad451 |
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author | Kakooza, Jackson Odur, Felix Ogei, Esau Taylor, Katrina Kalungi, Sam Lewis, Catherine R |
author_facet | Kakooza, Jackson Odur, Felix Ogei, Esau Taylor, Katrina Kalungi, Sam Lewis, Catherine R |
author_sort | Kakooza, Jackson |
collection | PubMed |
description | Rhabdomyosarcoma (RMS) is a soft tissue sarcoma that histologically resembles embryonic skeletal muscle. It can occur anywhere in the body, including tissues devoid of skeletal muscles. RMS is a common malignancy in children, and it accounts for ˃50% of all soft tissue sarcomas in children. Embryonal rhabdomyosarcoma (ERMS) mostly affects children younger than 10 years of age. The head and neck area, the genitourinary tract and the retroperitoneum are described as the preferred anatomic sites for ERMS development. However, the mesentery location is extremely rare. We report a rare case of an ERMS occurring in the mesentery of a 17-year-old male. |
format | Online Article Text |
id | pubmed-10409587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104095872023-08-09 Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report Kakooza, Jackson Odur, Felix Ogei, Esau Taylor, Katrina Kalungi, Sam Lewis, Catherine R J Surg Case Rep Case Report Rhabdomyosarcoma (RMS) is a soft tissue sarcoma that histologically resembles embryonic skeletal muscle. It can occur anywhere in the body, including tissues devoid of skeletal muscles. RMS is a common malignancy in children, and it accounts for ˃50% of all soft tissue sarcomas in children. Embryonal rhabdomyosarcoma (ERMS) mostly affects children younger than 10 years of age. The head and neck area, the genitourinary tract and the retroperitoneum are described as the preferred anatomic sites for ERMS development. However, the mesentery location is extremely rare. We report a rare case of an ERMS occurring in the mesentery of a 17-year-old male. Oxford University Press 2023-08-08 /pmc/articles/PMC10409587/ /pubmed/37560601 http://dx.doi.org/10.1093/jscr/rjad451 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kakooza, Jackson Odur, Felix Ogei, Esau Taylor, Katrina Kalungi, Sam Lewis, Catherine R Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
title | Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
title_full | Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
title_fullStr | Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
title_full_unstemmed | Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
title_short | Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
title_sort | mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409587/ https://www.ncbi.nlm.nih.gov/pubmed/37560601 http://dx.doi.org/10.1093/jscr/rjad451 |
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