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Cardiac Amyloid for the Internist
Hassan Ashraf1, Adam Hafeez2, Juan Vilaro2
1Internal Medicine, University of Florida College of Medicine, Gainesville, USA.
Insights
Cardiac amyloidosis, a rare cause of diastolic dysfunction, requires early clinical suspicion for accurate diagnosis and distinct management. Recognizing its infiltrative cardiomyopathy is crucial for improving patient outcomes.
Area of Science:
- Cardiology
- Internal Medicine
- Cardiomyopathy
Background:
- Cardiac amyloidosis is an infiltrative cardiomyopathy.
- It is an uncommon cause of diastolic dysfunction, associated with significant morbidity and mortality.
- Management differs from typical heart failure with preserved ejection fraction.
Abstract:
Cardiac amyloid is an uncommon cause of diastolic dysfunction the recognition of which requires the internist to have clinical suspicion to guide diagnosis and treatment. Cardiac amyloid is an infiltrative cardiomyopathy with significant morbidity and mortality. Appropriate diagnosis is important because management of cardiac amyloid differs from typical heart failure with preserved ejection fraction. An astute internist must be able to recognize common findings of cardiac amyloidosis. Here we present a case of a patient presenting with diastolic heart failure and the steps leading towards diagnosis and subsequent treatment.
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