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Published on: October 14, 2016
Recurrent primary cardiac osteosarcoma: a case report and literature review
Andrea Dell'Amore1, Nizar Asadi, Guido Caroli
1Thoracic Surgery Unit, S.Orsola Malpighi Hospital, University of Bologna, Via Massarenti 9, Bologna, Italy, dellamore76@libero.it.
Insights
Primary cardiac osteosarcoma, an extremely rare malignant tumor, presents significant surgical challenges. Despite extensive treatment, recurrence remains a critical issue, highlighting the need for improved therapeutic strategies.
Area of Science:
- Cardiovascular Surgery
- Surgical Oncology
- Cardiac Pathology
Background:
- Primary malignant cardiac tumors are exceptionally rare, with sarcomas being the most common subtype.
- Primary cardiac osteosarcoma is exceedingly rare, with only 42 cases documented globally.
- Surgical management of cardiac sarcomas is complex due to tumor location and proximity to vital structures, often yielding suboptimal results.
Observation:
- A case of recurrent primary cardiac osteosarcoma in a young male is presented.
- The patient underwent a complex surgical procedure involving trans-sternal right pneumonectomy and wide resection of the left and right atrium.
- Reconstruction was performed using heterologous pericardium under extracorporeal circulation.
Findings:
- Despite aggressive surgical intervention, the patient experienced local and systemic disease recurrence.
- The patient succumbed to the disease six months post-operation.
- This case underscores the aggressive nature and poor prognosis associated with recurrent primary cardiac osteosarcoma.
Implications:
- Current multimodality treatment strategies for cardiac sarcoma remain suboptimal.
- The challenges in achieving complete tumor resection with adequate margins necessitate further research into novel therapeutic approaches.
- Improved surgical techniques and adjuvant therapies are crucial for enhancing outcomes in patients with primary cardiac osteosarcoma.
Abstract:
Primary malignant cardiac tumors are very rare. Among malignant tumors, sarcomas occupy first place. In particular, primary cardiac osteosarcoma is extremely rare. To the best of our knowledge, only 42 cases have been reported worldwide. Cardiac malignant tumors usually require complex operations due to the difficulty in completely removing the tumor with acceptable free surgical margins and because of the proximity to vital structures. The current multimodality treatment strategies for cardiac sarcoma are still suboptimal, and surgery in particular frequently has unsatisfactory results. We report a case of recurrent primary cardiac osteosarcoma in a young male who underwent trans-sternal right pneumonectomy and a wide resection of the left and right atrium followed by reconstruction with heterologous pericardium under extracorporeal circulation. The patient died 6 months after the operation due to local and systemic disease recurrence.
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