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Multimodality imaging in cardiac amyloidosis: State-of-the-art review
Ana Teresa Timóteo1,2, Silvia Aguiar Rosa1,3, Pedro Garcia Brás1
1Cardiology Department, Santa Marta Hospital, Centro Hospitalar Universitário Lisboa Central, Lisbon, Portugal.
Cardiac amyloidosis (CA) diagnosis requires high suspicion and multimodality imaging. Echocardiography, MRI, scintigraphy, and CT confirm CA subtypes for effective treatment planning.
Area of Science:
- Cardiology
- Radiology
- Medical Imaging
Background:
- Amyloidosis is a systemic disease involving amyloid fibril deposition in organs, notably the heart.
- Cardiac amyloidosis (CA) presents challenges in diagnosis, necessitating high clinical suspicion.
- Early detection is crucial for initiating timely and effective treatment strategies.
Purpose of the Study:
- To review the role of multimodality imaging in diagnosing cardiac amyloidosis.
- To highlight the latest applications of imaging techniques in CA evaluation.
- To provide a practical flowchart for the diagnostic process.
Main Methods:
- Comprehensive review of multimodality imaging techniques for CA.
- Inclusion of echocardiography, cardiac magnetic resonance, scintigraphy, and computed tomography.
- Analysis of recent advancements and applications in CA imaging.
Main Results:
- Multimodality imaging is essential for confirming CA diagnosis.
- Imaging modalities differentiate CA subtypes, guiding treatment decisions.
- Specific imaging features aid in identifying amyloid deposition patterns.
Conclusions:
- A systematic multimodality imaging approach is vital for accurate CA diagnosis.
- Understanding imaging characteristics is key to classifying CA subtypes.
- The reviewed evidence supports a structured diagnostic pathway for CA management.
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