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
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