A case report of intravenous leiomyomatosis extending into the heart

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• 作者：" href="/content/?Author=Y.+Itani%3cORF+RID%3d%22A1%22%3e">Y. Itani ; " href="/content/?Author=Yuko+Otsuka%3cORF+RID%3d%22A1%22%3e">Yuko Otsuka ; " href="/content/?Author=Fujio+Deguchi%3cORF+RID%3d%22A1%22%3e">Fujio Deguchi ; " href="/content/?Author=Shigeru+Watanabe%3cORF+RID%3d%22A1%22%3e">Shigeru Watanabe ; " href="/content/?Author=Yoshiaki+Masuda%3cORF+RID%3d%22A1%22%3e">Yoshiaki Masuda ; " href="/content/?Author=Akira+Miyazaki%3cORF+RID%3d%22A2%22%3e">Akira Miyazaki and " href="/content/?Author=Osahiro+Takahashi%3cORF+RID%3d%22A3%22%3e">Osahiro Takahashi
• 刊名：Heart and Vessels
• 出版年：2001
• 出版时间：October 2001
• 年：2001
• 卷：15
• 期：6
• 页码：291-294
• 全文大小：731 KB
• 刊物类别：Medicine
• 刊物主题：Medicine & Public Health
  Cardiology
  Cardiac Surgery
  Vascular Surgery
  Biomedical Engineering
  Interventional Radiology
  Ultrasound
  
• 出版者：Springer Japan
• ISSN：1615-2573

文摘

The patient was a 47-year-old woman who underwent total hysterectomy for uterine leiomyoma in 1994. Two years later, intracaval and intravenous tumors were found by ultrasonic cardiography, magnetic resonance imaging, enhanced chest computed tomography, and venography. The patient underwent total removal of these tumors. Pathological findings indicated that these tumors were leiomyomas. After comparing the present findings with those of similar cases in the literature, we concluded that our patient had intravenous leiomyomatosis extending into the heart.