• Title of article

    Intravenous Leiomyomatosis with Intracardiac Extension as a Rare Cause of Abdominal Pain in an Adult Patient: A Case Report

  • Author/Authors

    Kılıç, Şahhan Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Çınar, Tufan Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Çiçek, Vedat Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Asal, Suha Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Selçuk, Murat Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Keskin, Muhammed Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Güner, Mehtap Department of Pathology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Turan, Ahmet Department of Cardiovascular Surgery - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey , Orhan, Ahmet Lütfullah Department of Cardiology - Haydarpasa Sultan Abdülhamid Han Training and Research Hospital - Health Sciences University - Istanbul, Turkey

  • Pages
    4
  • From page
    178
  • To page
    181
  • Abstract
    Intravenous leiomyomatosis (IVL) is a rare and benign smooth muscle tumor that arises from intrauterine venules or the myometrium. We herein describe a 49-year-old woman with a history of myomectomy who developed abdominal pain. An intravascular mass with extension to the right atrium was detected in the inferior vena cava. The mass was surgically resected in a single stage under cardiopulmonary bypass. IVL features were indicated by subsequent histopathology. Postoperatively, the patient was diagnosed with massive pericardial effusion and treated with a pericardial window. At 3 months’ outpatient clinical follow-up, she was asymptomatic. This case indicates that the diagnosis of IVL with extension to the heart should be kept in mind in patients presenting with abdominal pain
  • Keywords
    Adult , Leiomyomatosis , Cardiac tumor
  • Journal title
    The Journal of Tehran University Heart Center (JTHC)
  • Serial Year
    2021
  • Record number

    2726849