Cardiac amyloidosis differential diagnosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]; Aarti Narayan, M.B.B.S [3]; Lakshmi Gopalakrishnan, M.B.B.S. [4]Syed Hassan A. Kazmi BSc, MD [5]
Overview
Cardiomyopathy with congestive heart failure is the most common presentation of cardiac amyloidosis. Other common causes of cardiomyopathy should be excluded, and cardiac amyloidosis should be considered in the absence of a history of myocaridal ischemia, myocardial infarction, or presence of coronary artery disease risk factors. Cardiac amyloidosis should be included in the differential diagnoses in patients with unexplained congestive heart failure who have no history of valvular heart disease, long-standing hypertension, or myocardial ischemia.
Differentiating Cardiac Amyloidosis from Other Diseases
Cardiac amyloidosis should be differentiated from the following:
- Hypertension
- Anderson-Fabry disease
- Hypertrophic cardiomyopathy
- Cardiac sarcoidosis
- Cardiac lymphoma
Cardiac Amyloidosis is Differentiated from the Above Disorders by the Presence of the Following:
- Presence of low voltage on the EKG. Other causes of a low QRS voltage are shown here.
- Echo features such as:
- Diffuse increased echogenicity
- Valve thickening
- Thickened interatrial septum
- Global late gadolinium enhancement (LGE) on MRI
Cardiac amyloidosis (AL and TTRwt) should be differentiated from other causes of heart failure:
Differential Diagnosis | History and Symptoms | Physical Examination | Laboratory Findings | Imaging Findings |
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Periorbital purpura: Often occurs with sneezing, coughing or with minor trauma. Indicates capillary involvement of AL type amyloidosis.
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