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Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts
Published on: March 12, 2020
[Papillary cardiac fibroelastoma. An unusual presentation]
Manuel Fernando Rodríguez-Ortega1, Elías José Jacobo-Valdivieso, Octavio Flores-Calderón
1Departamento de Cirugía Cardiovascular, Centro Médico Nacional "20 de Noviembre," Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mesones 48-6, Col. Centro, Deleg. Cuauhtémoc, 06080 México, D.F., Mexico. fro2411@hotmail.com
Papillary fibroelastoma, a rare heart tumor, can cause serious embolic events. Early detection via echocardiography and surgical resection offer a curative and well-tolerated treatment for this benign cardiac neoplasm.
Area of Science:
- Cardiology and Cardiac Surgery
- Oncology (Neoplasms)
Background:
- Papillary fibroelastoma is a rare, benign cardiac tumor first described in 1976.
- Clinical presentations vary, complicating diagnosis despite no age or gender predilection.
- Diagnosis relies on location, macroscopic, and microscopic tumor characteristics.
Observation:
- A male patient with diabetes and hypertension presented with ischemic heart disease and ventricular tachycardia.
- Echocardiography revealed left ventricular aneurysm and an unusual apical tumor.
- The tumor involved the septum and left ventricle.
Findings:
- Primary heart tumors are rare, with an incidence of 0.0017%.
- Common symptoms include chest pain, syncope, dyspnea, and arrhythmias.
- Echocardiography often incidentally detects these tumors.
Implications:
- Papillary fibroelastoma is a recognized cause of embolic phenomena.
- Prompt surgical resection is the curative treatment of choice.
- Surgical outcomes are precise and well-tolerated, often involving tumor removal and potential valve repair.
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