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Swinging cardiac calcified amorphous tumour arising from a calcified mitral annulus in a patient with normal renal
Quentin de Hemptinne1, Jean-Paul Bar2, Didier de Cannière3
1Department of Cardiology, CHU Saint-Pierre-Université Libre de Bruxelles, Brussels, Belgium.
Insights
A rare calcified amorphous tumor was surgically removed from a patient's heart after cardioembolic events. The patient recovered well, with no recurrence after 12 months.
Area of Science:
- Cardiology
- Cardiac Surgery
- Pathology
Background:
- Intracardiac masses can lead to serious complications such as cardioembolic events.
- Prompt diagnosis and management are crucial for patients presenting with embolic phenomena.
Observation:
- A 67-year-old male presented with two cardioembolic events.
- Imaging revealed a mobile intracardiac mass on the ventricular side of a calcified mitral annulus, not previously seen.
Findings:
- Surgical resection of the intracardiac mass was performed.
- Microscopic examination confirmed the mass as a calcified amorphous tumor.
- The patient experienced an unremarkable postoperative recovery.
Implications:
- Surgical excision is an effective treatment for calcified amorphous tumors of the heart.
- Complete resection leads to favorable long-term outcomes, preventing recurrence and neurological events.
- This case highlights the importance of thorough cardiac evaluation in patients with unexplained embolic events.
Abstract:
A 67-year-old man was referred to our institution for the management of a left-sided intracardiac mass discovered following two cardioembolic events. Imaging studies revealed a highly mobile mass attached to the ventricular side of a calcified mitral annulus. The mass had not been present on echocardiography 1 year earlier. Surgical resection was performed. Microscopic examination confirmed the diagnosis of a calcified amorphous tumour. The postoperative course was unremarkable, and the patient remains asymptomatic and without recurrence of a mass or neurological event after a 12-month follow-up.
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