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Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging

Rhabdomyosarcoma is an uncommon soft tissue sarcoma that rarely presents in adults. Clinical presentation is dependent on site and size. We present the case of a woman who presented with acute-onset dyspnoea and whose pathology report confirmed embryonal rhabdomyosarcoma (ERMS) seen as an incidental...

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Autores principales: Jain, Esha, Al-Tarbsheh, Ali Hani, Oweis, Jozef, Abdelwahab, Hala, Shkolnik, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668012/
https://www.ncbi.nlm.nih.gov/pubmed/34912733
http://dx.doi.org/10.12890/2021_002834
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author Jain, Esha
Al-Tarbsheh, Ali Hani
Oweis, Jozef
Abdelwahab, Hala
Shkolnik, Boris
author_facet Jain, Esha
Al-Tarbsheh, Ali Hani
Oweis, Jozef
Abdelwahab, Hala
Shkolnik, Boris
author_sort Jain, Esha
collection PubMed
description Rhabdomyosarcoma is an uncommon soft tissue sarcoma that rarely presents in adults. Clinical presentation is dependent on site and size. We present the case of a woman who presented with acute-onset dyspnoea and whose pathology report confirmed embryonal rhabdomyosarcoma (ERMS) seen as an incidental finding on chest computed tomography. We also describe the clinical, laboratory and radiological work-up conducted to diagnose and manage ERMS in the critical care setting. LEARNING POINTS: Rhabdomyosarcoma is a rare malignancy with a poor prognosis in adults compared with children, especially if it presents in an unfavourable primary site and has an unfavourable histological diagnosis. Immunohistochemical diagnosis remains the gold standard for embryonal rhabdomyosarcoma diagnosis and differentiation from similar malignancies on initial imaging studies. Management of adult rhabdomyosarcoma is usually multimodal with surgical resection and a combination of chemo and radiotherapy.
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spelling pubmed-86680122021-12-14 Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging Jain, Esha Al-Tarbsheh, Ali Hani Oweis, Jozef Abdelwahab, Hala Shkolnik, Boris Eur J Case Rep Intern Med Articles Rhabdomyosarcoma is an uncommon soft tissue sarcoma that rarely presents in adults. Clinical presentation is dependent on site and size. We present the case of a woman who presented with acute-onset dyspnoea and whose pathology report confirmed embryonal rhabdomyosarcoma (ERMS) seen as an incidental finding on chest computed tomography. We also describe the clinical, laboratory and radiological work-up conducted to diagnose and manage ERMS in the critical care setting. LEARNING POINTS: Rhabdomyosarcoma is a rare malignancy with a poor prognosis in adults compared with children, especially if it presents in an unfavourable primary site and has an unfavourable histological diagnosis. Immunohistochemical diagnosis remains the gold standard for embryonal rhabdomyosarcoma diagnosis and differentiation from similar malignancies on initial imaging studies. Management of adult rhabdomyosarcoma is usually multimodal with surgical resection and a combination of chemo and radiotherapy. SMC Media Srl 2021-11-24 /pmc/articles/PMC8668012/ /pubmed/34912733 http://dx.doi.org/10.12890/2021_002834 Text en © EFIM 2021 This article is licensed under a Commons Attribution Non-Commercial 4.0 License
spellingShingle Articles
Jain, Esha
Al-Tarbsheh, Ali Hani
Oweis, Jozef
Abdelwahab, Hala
Shkolnik, Boris
Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging
title Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging
title_full Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging
title_fullStr Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging
title_full_unstemmed Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging
title_short Incidental Discovery of Embryonal Rhabdomyosarcoma on CT Imaging
title_sort incidental discovery of embryonal rhabdomyosarcoma on ct imaging
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668012/
https://www.ncbi.nlm.nih.gov/pubmed/34912733
http://dx.doi.org/10.12890/2021_002834
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