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Multimodality imaging of vaginal rhabdomyosarcoma

Rhabdomyosarcoma (RMS) is a malignant mesenchymal tumor arising from the embryonal muscle cells (rhabdomyoblasts), and is the most common soft tissue sarcoma in children and young adults accounting for 4–6% of all malignancies in this age group. Though rare overall, embryonal rhabdomyosarcoma is the...

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Autores principales: Chauhan, Richa S, Singh, Dheeraj K, Guha, Bishwarup, Kumar, Ishan, Verma, Ashish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510311/
https://www.ncbi.nlm.nih.gov/pubmed/28744074
http://dx.doi.org/10.4103/ijri.IJRI_444_16
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author Chauhan, Richa S
Singh, Dheeraj K
Guha, Bishwarup
Kumar, Ishan
Verma, Ashish
author_facet Chauhan, Richa S
Singh, Dheeraj K
Guha, Bishwarup
Kumar, Ishan
Verma, Ashish
author_sort Chauhan, Richa S
collection PubMed
description Rhabdomyosarcoma (RMS) is a malignant mesenchymal tumor arising from the embryonal muscle cells (rhabdomyoblasts), and is the most common soft tissue sarcoma in children and young adults accounting for 4–6% of all malignancies in this age group. Though rare overall, embryonal rhabdomyosarcoma is the most common malignancy arising in the pediatric female genitourinary tract with sarcoma botryoides being the most common variant of the tumor. In young and adolescent individuals, the cervix and uterus are affected; whereas in infants, vaginal lesions are more common. Imaging plays a crucial role not only in the initial diagnosis but also in long-term follow-up of genital RMS. We describe a rare case of embryonal rhabdomyosarcoma of the vagina occurring in a 23-year-old female who presented with abnormal vaginal bleeding ever since she was a child.
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spelling pubmed-55103112017-07-25 Multimodality imaging of vaginal rhabdomyosarcoma Chauhan, Richa S Singh, Dheeraj K Guha, Bishwarup Kumar, Ishan Verma, Ashish Indian J Radiol Imaging Genitourinary Radiology Rhabdomyosarcoma (RMS) is a malignant mesenchymal tumor arising from the embryonal muscle cells (rhabdomyoblasts), and is the most common soft tissue sarcoma in children and young adults accounting for 4–6% of all malignancies in this age group. Though rare overall, embryonal rhabdomyosarcoma is the most common malignancy arising in the pediatric female genitourinary tract with sarcoma botryoides being the most common variant of the tumor. In young and adolescent individuals, the cervix and uterus are affected; whereas in infants, vaginal lesions are more common. Imaging plays a crucial role not only in the initial diagnosis but also in long-term follow-up of genital RMS. We describe a rare case of embryonal rhabdomyosarcoma of the vagina occurring in a 23-year-old female who presented with abnormal vaginal bleeding ever since she was a child. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5510311/ /pubmed/28744074 http://dx.doi.org/10.4103/ijri.IJRI_444_16 Text en Copyright: © 2017 Indian Journal of Radiology and Imaging http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Genitourinary Radiology
Chauhan, Richa S
Singh, Dheeraj K
Guha, Bishwarup
Kumar, Ishan
Verma, Ashish
Multimodality imaging of vaginal rhabdomyosarcoma
title Multimodality imaging of vaginal rhabdomyosarcoma
title_full Multimodality imaging of vaginal rhabdomyosarcoma
title_fullStr Multimodality imaging of vaginal rhabdomyosarcoma
title_full_unstemmed Multimodality imaging of vaginal rhabdomyosarcoma
title_short Multimodality imaging of vaginal rhabdomyosarcoma
title_sort multimodality imaging of vaginal rhabdomyosarcoma
topic Genitourinary Radiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510311/
https://www.ncbi.nlm.nih.gov/pubmed/28744074
http://dx.doi.org/10.4103/ijri.IJRI_444_16
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