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Rhabdomyosarcoma from uterus to heart
Rhabdomyosarcoma (RMS) is a malignant soft tissue tumor of the pediatric population which is  rarely seen in adults. Metastatic rhabdomyosarcoma is even rarer. We present an unusual case of a 49 year old female presenting with palpitations and uterine bleeding. An Echo-cardiogram revealed a large o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426992/ https://www.ncbi.nlm.nih.gov/pubmed/32850073 http://dx.doi.org/10.1080/20009666.2020.1760465 |
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author | Roomi, Sohaib Sherazi, Mahnoor Fatima Ullah, Waqas Khan, Omair Ali Minalyan, Artem Atiq, Muhammad Thalambedu, Nishant |
author_facet | Roomi, Sohaib Sherazi, Mahnoor Fatima Ullah, Waqas Khan, Omair Ali Minalyan, Artem Atiq, Muhammad Thalambedu, Nishant |
author_sort | Roomi, Sohaib |
collection | PubMed |
description | Rhabdomyosarcoma (RMS) is a malignant soft tissue tumor of the pediatric population which is  rarely seen in adults. Metastatic rhabdomyosarcoma is even rarer. We present an unusual case of a 49 year old female presenting with palpitations and uterine bleeding. An Echo-cardiogram revealed a large oval mass on the posterior mitral leaflet and a Computerized Tomography (CT) scan of the abdomen revealed a uterine growth. Surgical excision of the cardiac mass was done and histological analysis of cardiac lesion confirmed it to be rhabdomyosarcoma with a primary source in the uterus. The patient became asymptomatic from a cardiac standpoint after excision of the mass and was scheduled for chemo/radiation therapy for the primary uterine malignancy. Metastatic cardiac rhabdomyosarcoma can be confused with a myxoma or any other primary or secondary cardiac tumors resulting in delayed diagnosis. However, its aggressive nature makes it a life-threatening tumor that requires an early diagnosis to prevent fatal consequences. |
format | Online Article Text |
id | pubmed-7426992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74269922020-08-25 Rhabdomyosarcoma from uterus to heart Roomi, Sohaib Sherazi, Mahnoor Fatima Ullah, Waqas Khan, Omair Ali Minalyan, Artem Atiq, Muhammad Thalambedu, Nishant J Community Hosp Intern Med Perspect Case Report Rhabdomyosarcoma (RMS) is a malignant soft tissue tumor of the pediatric population which is  rarely seen in adults. Metastatic rhabdomyosarcoma is even rarer. We present an unusual case of a 49 year old female presenting with palpitations and uterine bleeding. An Echo-cardiogram revealed a large oval mass on the posterior mitral leaflet and a Computerized Tomography (CT) scan of the abdomen revealed a uterine growth. Surgical excision of the cardiac mass was done and histological analysis of cardiac lesion confirmed it to be rhabdomyosarcoma with a primary source in the uterus. The patient became asymptomatic from a cardiac standpoint after excision of the mass and was scheduled for chemo/radiation therapy for the primary uterine malignancy. Metastatic cardiac rhabdomyosarcoma can be confused with a myxoma or any other primary or secondary cardiac tumors resulting in delayed diagnosis. However, its aggressive nature makes it a life-threatening tumor that requires an early diagnosis to prevent fatal consequences. Taylor & Francis 2020-06-14 /pmc/articles/PMC7426992/ /pubmed/32850073 http://dx.doi.org/10.1080/20009666.2020.1760465 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Roomi, Sohaib Sherazi, Mahnoor Fatima Ullah, Waqas Khan, Omair Ali Minalyan, Artem Atiq, Muhammad Thalambedu, Nishant Rhabdomyosarcoma from uterus to heart |
title | Rhabdomyosarcoma from uterus to heart |
title_full | Rhabdomyosarcoma from uterus to heart |
title_fullStr | Rhabdomyosarcoma from uterus to heart |
title_full_unstemmed | Rhabdomyosarcoma from uterus to heart |
title_short | Rhabdomyosarcoma from uterus to heart |
title_sort | rhabdomyosarcoma from uterus to heart |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426992/ https://www.ncbi.nlm.nih.gov/pubmed/32850073 http://dx.doi.org/10.1080/20009666.2020.1760465 |
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