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Related Experiment Video

Updated: May 19, 2026

Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques

Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques

Published on: June 11, 2019

Biatrial myxomas with Carney complex.

Yukiko Yamada¹, Hideki Sasaki, Takashi Tominaga

¹Department of Cardiovascular Surgery, Ehime Prefectural Central Hospital, 83 Kasuga-cho Matsuyama-si Ehime 790-0024, Japan.

Asian Cardiovascular & Thoracic Annals

|August 11, 2012

Summary

This summary is machine-generated.

A patient with chest pain was diagnosed with cardiac myxomas and pulmonary embolism. Subsequent findings revealed Carney complex, a rare condition involving multiple myxomas and acromegaly.

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Area of Science:

Cardiology
Endocrinology
Genetics

Background:

Cardiac myxomas are rare primary tumors of the heart.
Pulmonary embolism is a serious condition often associated with cardiac abnormalities.
Carney complex is a genetic disorder predisposing individuals to myxomas and other tumors.

Observation:

A 30-year-old man presented with chest pain.
Bi-atrial myxomas and pulmonary embolism were diagnosed.
Histological examination confirmed multiple cardiac myxomas.

Findings:

The patient exhibited spotty pigmentations and cutaneous myxomas.
Acromegaly was also identified.
The constellation of findings led to a diagnosis of Carney complex.

Implications:

This case highlights the importance of a comprehensive evaluation for patients with cardiac myxomas.
Early diagnosis of Carney complex is crucial for managing associated risks.
Multidisciplinary care is essential for patients with Carney complex.