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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...

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Autores principales: Kakooza, Jackson, Odur, Felix, Ogei, Esau, Taylor, Katrina, Kalungi, Sam, Lewis, Catherine R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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