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Published on: June 11, 2019
Giant and multiple cardiac papillary fibroelastomas masquerading as acute cerebrovascular events
Cosmin Adrian Teodoru1, Maria Alexandra Preda, Veronica Mădălina Borugă
1Department of Ophthalmology, Department of Biochemistry, Victor Babeş University of Medicine and Pharmacy, Timişoara, Romania; sutamarius@yahoo.ro, dia_bonte@yahoo.com.
Insights
Cardiac papillary fibroelastomas, rare benign heart tumors, pose a high risk of embolization. This report details two unusual cases, highlighting their significant size and multiplicity, which are uncommon presentations.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Cardiac papillary fibroelastomas (CPF) are uncommon benign neoplasms of the heart.
- These tumors are clinically significant due to their high embolic potential, leading to severe complications.
- While rare, CPF can present with varying sizes and numbers, posing diagnostic and therapeutic challenges.
Purpose of the Study:
- To report two rare cases of cardiac papillary fibroelastomas.
- To emphasize the unusual size and multiplicity of these tumors in the presented cases.
- To discuss the clinical implications and management of such rare presentations.
Main Methods:
- Case report presentation.
- Review of clinical data and imaging findings.
- Pathological examination of resected tumors (if applicable).
Main Results:
- Two patients presented with cardiac papillary fibroelastomas.
- The tumors were notably large and multiple, which is an infrequent occurrence.
- Embolic events or risk thereof were a primary clinical concern.
Conclusions:
- Cardiac papillary fibroelastomas, despite being benign, require careful management due to embolic risks.
- Unusually large or multiple CPF represent a rare but significant clinical scenario.
- Early diagnosis and appropriate intervention are crucial for preventing embolic complications.
Abstract:
Cardiac papillary fibroelastomas are rare benign cardiac tumors. Their clinical significance results from their very high propensity for embolization. We present two such cases, which are rare regarding the size and multiplicity of these tumors.
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