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Cardiac Sarcoidosis

An inflammatory cardiomyopathy in which non-caseating granulomas of sarcoidosis involve the myocardium, conduction system, or pericardium and may cause heart block, arrhythmia, and heart failure.

Written by: Saygı Hospital Health Guide Editorial Board
Last updated:

This content has been compiled by the Saygı Hospital Health Guide Editorial Board and is periodically reviewed by a specialist physician.

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This content is for informational purposes only and does not constitute medical advice. You can book an appointment at our Dahiliye (İç Hastalıkları) department. Book Appointment →

What is Cardiac Sarcoidosis?

Cardiac sarcoidosis is a manifestation of systemic sarcoidosis in which non-caseating granulomas infiltrate the myocardium, with predilection for the basal interventricular septum, the left ventricular free wall, and the conduction system.

Clinical phenotypes range from asymptomatic patients with abnormal cardiac MRI findings to atrioventricular block, sustained ventricular tachycardia, dilated cardiomyopathy, and sudden cardiac death; up to 25 percent of patients with extracardiac sarcoidosis have subclinical cardiac involvement.

Diagnosis combines tissue biopsy of an extracardiac site, late gadolinium enhancement on cardiac MRI, focal FDG uptake on cardiac PET-CT after specific dietary preparation, and exclusion of alternative causes; treatment is based on corticosteroids, steroid-sparing immunosuppressants, and device therapy when indicated.

Symptoms

New-onset palpitations, syncope, or near-syncope episodes
Progressive dyspnea on exertion or symptoms of heart failure
Atrioventricular block, especially in patients younger than 60 years
Sustained or non-sustained ventricular tachycardia
Chest discomfort and reduced exercise tolerance
Constitutional symptoms of systemic sarcoidosis such as fatigue, weight loss, or low-grade fever

Risk Factors

Established diagnosis of pulmonary or systemic sarcoidosis
African and Japanese ancestry, with higher prevalence and severity
Multi-organ sarcoid involvement, particularly skin, eye, or central nervous system
Family history of sarcoidosis
Adult age between 25 and 60 years

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Unexplained syncope or new high-grade atrioventricular block in a young or middle-aged adult — urgent cardiology evaluation
  • Sustained palpitations or documented ventricular arrhythmia in a patient with known sarcoidosis
  • New heart failure or cardiomyopathy of unclear etiology
  • Abnormal cardiac MRI or FDG-PET findings discovered during evaluation of systemic sarcoidosis

Treatment Methods

01
Corticosteroid therapy (prednisone) as first-line immunosuppression to control active inflammation
02
Steroid-sparing agents such as methotrexate, azathioprine, or mycophenolate for maintenance and to reduce steroid toxicity
03
Implantable cardioverter-defibrillator (ICD) for ventricular arrhythmia or significant scar burden, and pacemaker for high-grade atrioventricular block
04
Guideline-directed heart failure therapy when left ventricular function is impaired
05
Catheter ablation for refractory ventricular tachycardia and consideration of advanced heart failure therapies, including transplantation, in end-stage disease

Which Department to Visit?

You can visit our Dahiliye (İç Hastalıkları) department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.

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Health Disclaimer: The information on this page is prepared for general informational purposes only. It does not replace medical diagnosis and treatment. Please consult your physician for your complaints. Saygı Hospital does not accept responsibility for actions taken based on the information on this page.