Wild-type (senile) amyloidosis differential diagnosis: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{Wild-type (senile) amyloidosis}}
{{Wild-type (senile) amyloidosis}}
{{CMG}}
{{CMG}}{{AE}}


==Overview==
==Overview==

Revision as of 20:32, 19 December 2019

Wild-type (senile) amyloidosis Microchapters

Home

Patient Information

Overview

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

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Wild-type (senile) amyloidosis differential diagnosis On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Wild-type (senile) amyloidosis differential diagnosis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Wild-type (senile) amyloidosis differential diagnosis

CDC on Wild-type (senile) amyloidosis differential diagnosis

Wild-type (senile) amyloidosis differential diagnosis in the news

Blogs on Wild-type (senile) amyloidosis differential diagnosis

Directions to Hospitals Treating Psoriasis

Risk calculators and risk factors for Wild-type (senile) amyloidosis differential diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief:

Overview

Differentiating Wild-type (Senile) Amyloidosis from other Diseases

Differentials Based on Cardiac Involvement (Heart Failure)

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
Cardiac amyloidosis
  • Elevated jugular pressure

Periorbital purpura: Often occurs with sneezing, coughing or with minor trauma. Indicates capillary involvement of AL type amyloidosis.

  • Macroglossia
  • Abnormal phonation
  • Hepatomegaly
  • Ascites may be present in the setting of heart failure
  • Valvular involvement murmurs of mitral and tricuspid regurgitation (systolic).


  • Normocytic mormochromic anemia
  • Serum free-light-chain assay positive
  • Increased BNP, ANP and β2 microglobulin
  • Voltage-to-mass ratio is more sensitive than EKG, 2D Echo and nuclear scanning alone
Cardiac sarcoidosis
  • Asymptomatic conduction abnormalities
  • Chest pain
  • Congestive heart failure symptoms:
    • Fatigue
    • Syncope
    • Dyspnea
    • Chest pain.
    • Irregular heartbeats
    • Palpitations
    • edema
  • Ventricular tachyarrhythmia
  • Heart block
  • Valvular regurgitation
  • Pericardial effusion
  • Constrictive pericarditis or temponade
  • Serum markers that have been reported as markers of sarcoidosis in general are:
    • Serum amyloid A (SAA)
    • Soluble interleukin-2 receptor (sIL-2R)
    • Lysozyme
    • Angiotensin-converting enzyme (ACE)
    • Gycoprotein KL-6
    • Hypercalcemia
    • Hypercalciuria
    • (noncaseating granulomas secrete 1,25 vitamin D)
  • Radionuclide examinations
    • Thallium‐201 scintigraphy
    • Gallium‐67 scintigraphy
    • Positron emission tomography
  • Magnetic resonance imaging
  • Samples of myocardium with sarcoidosis shows the following:
  • Non‐caseating, multinucleated giant cell granuloma in the subendocardium
  • Trichrome stain can show a dense band of collagen fibers, encasing aggregate of granulomas and inflammatory cells
ST Segment Elevation Myocardial Infarction
  • Chest pain with possible radiation to left arm and lower jaw
  • Squeezing, crushing chest pain
  • Sweating
  • Nausea and vomiting
  • Anxious patient in pain with diaphoresis
  • Signs of heart failure may be present
  • Arrhythmia
  • ST elevation, new left bundle branch block, and Q wave on EKG
  • Elevated cardiac biomarkers
  • Either complete or subtotal occlusion of an epicardial coronary artery on coronary angiography
  • Confluent hyperenhancement extending from the endocardium
Non ST Elevation Myocardial Infarction
  • Crushing, left-sided substernal chest pain or pressure that radiates to the neck or left arm
  • Same as ST-elevation MI
  • ST-segment depression or T-wave inversion on EKG
  • Elevated cardiac biomarkers
Pericarditis
  • Chest pain relieved by sitting up and leaning forward and worsened by lying down
  • Fever, anxiety, difficulty breathing
  • Pericardial friction rub
  • Signs of cardiac tamponade may be present
  • PR segment depression and electrical alternans on EKG
  • A flask-shaped, enlarged cardiac silhouette on CXR
  • Pericardial thickness of more than 4 mm on MRI
  • Pericardial effusion and cardiac chamber indentation or collapse on echo when cardiac tamponade is present
Alcoholic Cardiomyopathy
  • History of alcohol abuse
  • Fatigue, weakness, anorexia, palpitations, and shortness of breath on activity
  • Leg swelling and pedal edema
  • Signs of heart failure such as presence of S3 and S4 heart sounds, pedal edema, and jugular venous distension
  • Signs of alcoholic liver disease may be present
  • Elevated MCV and MCHC on CBC
  • Elevated LDH, AST, ALT, creatine kinase, gammaglutamyl transpeptidase, malic dehydrogenase, and alpha-hydroxybutyric dehydrogenase
  • Q waves and non specific ST and T wave changes on EKG
  • Cardiomegaly, pulmonary congestion, and pleural effusions on CXR
  • Left ventricular dilatation on echo


References