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Updated: Feb 15, 2026

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Four-Dimensional Computed Tomography-Guided Valve Sizing for Transcatheter Pulmonary Valve Replacement
Published on: January 20, 2022
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Primary pulmonary valve papillary fibroelastoma.
Satoshi Tobe1, Kazunori Yoshida, Masahiro Yamaguchi
1Department of Cardiovascular Surgery, Akashi Medical Center, Akashi, Hyogo, Japan.
Summary
Papillary fibroelastoma, a benign cardiac tumor, can cause serious embolic events. Early detection and surgical removal of these pulmonary artery tumors are crucial for patient survival.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Papillary fibroelastoma (PFE) is a rare, benign cardiac tumor originating from the valvular endocardium.
- PFEs are often discovered incidentally during echocardiography or cardiac surgery.
- While histologically benign, PFEs pose a risk of significant embolic complications.
Observation:
- A 73-year-old male patient with a history of hepatocellular carcinoma presented with an incidentally detected 2.5-cm mass in the pulmonary trunk.
- The mass was located superior to the pulmonary valve, specifically on the commissure of the right and posterior pulmonary cusp.
- Echocardiography confirmed the presence and location of the cardiac tumor.
Findings:
- Surgical excision of the pulmonary trunk mass was performed via a transpulmonary arterial approach with cardiopulmonary bypass.
- Histopathological examination confirmed the diagnosis of papillary fibroelastoma.
- The tumor was successfully removed along with the involved endocardium.
Implications:
- Papillary fibroelastomas, despite their benign nature, can lead to life-threatening embolic events, including stroke, myocardial infarction, and pulmonary embolism.
- Prompt identification and surgical resection of cardiac tumors like PFE are critical for preventing potentially fatal embolic complications.
- This case highlights the importance of vigilant cardiac surveillance, particularly in patients with a history of malignancy or other risk factors.
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