Successful Surgical Treatment of an Aggressive Pelvic Angiomyxoma With Intracardiac Extension.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 28633254.
- Also identified by DOI 10.1016/j.athoracsur.2017.01.118.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
We present a case of an intravenous tumor with extension into the right atrium and right ventricle of the heart. Pelvic angiomyxoma is a rare benign tumor, which in this case carried a significant operative risk due to its extension. The patient initially presented with suspected caval and intracardiac thrombus, but unsuccessful treatment led to further investigations. The tumor was extensively dissected from the right atrium, suprarenal vena cava, and left iliac vein on cardiopulmonary bypass and deep hypothermic circulatory arrest. Affected gynecological organs were removed. The patient recovered uneventfully and received hormonal therapy postoperatively.
Medical subject headings
- Cardiac Surgical Procedures
- Heart Neoplasms
- Myxoma
- Pelvic Neoplasms