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Updated: Aug 29, 2025

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
The Syncopal Sarcoma: A Rare Case of Primary Cardiac Synovial Sarcoma
Adam J Eqbal1, Laura Goodliffe2, Hassan Masoom2
1Division of Cardiac Surgery, McMaster University, Hamilton, Ontario, Canada.
Insights
Primary cardiac synovial sarcoma is an extremely rare tumor. This case highlights a large intracardiac tumor causing syncope and obstructive shock in a young adult.
Area of Science:
- Cardiovascular Medicine
- Oncology
Background:
- Primary cardiac tumors are rare, with synovial sarcomas accounting for less than 1% of these neoplasms.
- Synovial sarcoma is a soft tissue sarcoma that rarely originates in the heart.
Observation:
- A 19-year-old male presented with syncope and dynamic obstructive shock.
- A large, right-sided intracardiac tumor was identified as the cause of the patient's symptoms.
Findings:
- The intracardiac mass was diagnosed as a primary cardiac synovial sarcoma.
- The tumor's size and location led to significant hemodynamic compromise.
Implications:
- This case underscores the importance of considering rare cardiac tumors in the differential diagnosis of unexplained syncope and shock.
- Early diagnosis and management are crucial for patients with primary cardiac synovial sarcoma due to its potential for rapid progression and poor prognosis.
Abstract:
Primary cardiac synovial sarcomas are very rare, representing <1% of all primary cardiac tumors. We report the case of a 19-year-old man with syncope and dynamic obstructive shock caused by a large right-sided intracardiac tumor. (Level of Difficulty: Beginner .).
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