alexa Cardiac Metastasis of Uterine Leiomyosarcoma: Case Report and Literature Review
ISSN: 2471-8556

Oncology & Cancer Case Reports
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Case Report

Cardiac Metastasis of Uterine Leiomyosarcoma: Case Report and Literature Review

Hassaniya Zmaimita1*, Hamza Samlali1, Awatif Rachdi1, Amina Taleb1, Zineb Bouchbika1, Nadia Benchekroune1, Hassan Jouhadi1, NezhaTawfiq1, Souha Sahraoui1, Abdellatif Benider1and Fadoua El Mansouri2

1The University Hospital, Mohamed VI Centre of Cancer Treatments, Casablanca, Morocco

2Anatomopathological Laboratory of Goulmima, Casablanca, Morocco

*Corresponding Author:
Hassaniya Zmaimita
The University Hospital
Mohamed VI Centre of Cancer Treatments
Casablanca, Morocco
Tel: +2120537661055
E-mail: [email protected]

Received Date: November 07, 2016; Accepted Date: January 17, 2017; Published Date: January 20, 2017

Citation: Zmaimita H, Samlali H, Rachdi A, Taleb A, Bouchbika Z, et al. (2017) Cardiac Metastasis of Uterine Leiomyosarcoma: Case Report and Literature Review. Oncol Cancer Case Rep 3:123. doi: 10.4172/2471-8556.1000123

Copyright: © 2017 Zmaimita H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Uterine leiomyosarcoma is a very rare tumor. The risk of developing metastasis is high especially for lung. Some localizations are possible but infrequent. The heart is not a body filter and cardiac metastases are exceptional. We are reporting a case of a 57 years old female patient who had cardiac metastasis of an uterine leiomyosarcoma. Postmenopausal bleeding revealed the uterine tumor. The cardiac metastasis was discovered during an echocardiography indicated for pre-chemotherapy cardiac work-up. A magnetic resonance imaging revealed a mass connection between the mitral valve and the aortic sigmoid. The patient was placed on chemotherapy. Cardiac metastasis of a uterine leiomyosarcoma are very rare and have been rarely reported in the literature. The presence of cardiac metastasis in a patient need to be discussed inside a multidisciplinary committee before any symptoms.

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