A primary cardiac tumor is extremely rare. The majority of primary cardiac tumors are benign, and approximately onequarter are malignant. The most common type of cardiac tumor is cardiac myxoma, which is usually located in the left atrium. Aside from the above, the majority of these malignant tumors are sarcomas, which can be distinguished by their different histologies. However, the differential diagnosis between benign myxomas and malignant sarcomas might be challenging in certain cases, and a high index of clinical suspicion and vimentin staining can be useful in making the diagnosis. In this case report, we present a young female who received an operation for a tumor of the left atrium that was initially diagnosed as a myxoma but later recurred as a myxofibrosarcoma. As a consequence of the immunoreactive results of MDM2 amplification, cardiac intimal sarcoma was finally diagnosed. It is notable that surgical removal of the primary tumor with extensive cryoablation of horizontal tumor spreading using a cryoballoon and cryoablation probe, which are initially designed for pulmonary vein isolation and Maze procedure, incorporated with postoperative radiotherapy, chemotherapy, and surgery to remove the costal bone metastasis effectively prevents the disease from relapsing and recurrences.