Wild-type (senile) amyloidosis overview

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Wild-type (senile) amyloidosis was previously referred to as senile systemic amyloidosis (SSA) or senile cardiac amyloidosis (SCA). It is characterized by the deposition of transthyretin (TTR), a protein that is primarily made in the liver, throughout the body. The most common location of deposition of this protein is the heart. As the name suggests, this disease is encountered among the elderly population. The fact that this condition is more commonly found in the elderly population complicates the diagnosis making process as this affected population is usually at risk of and/or affected by cardiovascular diseases.

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Wild-type (senile) amyloidosis from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications, and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

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