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
Link To Document :
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