Amyloid light chain (AL) amyloidosis is a rare, debilitating, often fatal disease. Symptoms of
cardiomyopathy are common presenting features, and patients often are referred to …

Systemic Light chain (AL) amyloidosis is a monoclonal plasma cell proliferative disorder
characterized by deposition of amyloidogenic monoclonal light chain fragments causing …

Cardiac amyloidosis is one form of systemic amyloidosis caused by abnormal amyloid fibrils
deposited in the extracellular space of the myocardium causing heart failure because of …

Background Diagnosis of cardiac amyloidosis (CA) is often delayed due to variability in
clinical presentation. The electrocardiogram (ECG) is one of the most common and widely …

Cardiac amyloidosis (CA) occurs when the insoluble fibrils formed by misfolded precursor
proteins deposit in cardiac tissues. The early clinical manifestations of CA are not evident …

Multiple myeloma (MM) is a hematologic malignancy characterized by the abnormal clonal
proliferation of plasma cells that may result in focal bone lesions, renal failure, anemia …

Wild‐type transthyretin amyloid cardiomyopathy (ATTRwt CM) is a more common disease
than previously thought. Awareness of ATTRwt CM and its diagnosis has been challenged …

Determining the etiologies of left ventricular hypertrophy (LVH) can be challenging due to
the similarities of the different manifestations in clinical presentation and morphological …

Objectives: Summarize the epidemiology of transthyretin amyloid cardiomyopathy.. Explain
the common cardiac and non-cardiac findings associated with transthyretin amyloid …

Aim Amyloidosis is a systemic or localized disease of protein deposition characterized by
amorphous eosinophilic morphology and positivity of Congo Red staining. The typing of …