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Outline
Intravenous leiomyomatosis of the ut erus with extension to the right heart: A case report
Authors
1Associated Professor, Department of Pathology, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehra n, Iran, Andorra
2Assistant Professor, Department of Pathology, Besat Hospital, AJA University of Medical Sciences, Tehran, Iran, Andorra
3Researcher, AJA University of Medical Sciences, Tehran, Iran, Andorra
4Researcher, Department of Pathology, Imam Khomeini Ho spital, Tehran University of Medical Sciences, Tehran, Iran, Andorra
*Corresponding Author: Corresponding author: Katayoun Ziyari, Assistant Professor, Department of Pathology, Besat Hospital, AJA University of Medical Sciences, Tehran, Iran, Andorra Email: drk_ziari@yahoo.com
Published online:Mar 11, 2013
Article type:Case Report
Received:Nov 21, 2012
Accepted:Feb 11, 2013
How to Cite:Haeri H, Ziyari K, Alizadeh K, Vosoghi B. Intravenous leiomyomatosis of the ut erus with extension to the right heart: A case report. Ann Mil Health Sci Res. 2013;11(1):e67461. doi:
Abstract
Intravenous leiomyomatosis is an uncommon non-malignant tumor which originates from the smoo th muscle cells. It is usually confined to the pelvic venous system. Rarely it can afflict intracaval and intracardiac extension. We report a case of young 25 years old woman, G2/P2; with intravenous leiomyom atosis originate from the uterus and extending into right atrium. It was successfully treated through a two-stage surgical approac h. In conclusion, we should consider intravenous leiomyomatosis with cardiac extension in patient with uterus leiomyoma, hysterectomy, cardiac symptoms, and cardiac ma ss.
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Copyright
© 2013, Annals of Military and Health Sciences Research. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.
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