What is cardiac sarcoidosis?
Cardiac sarcoidosis is a condition in which granulomas, which are clusters of inflammatory cells, form in the heart tissue as part of a systemic disease called sarcoidosis. This can lead to inflammation and scarring in the heart, affecting its function.
What causes cardiac sarcoidosis?
The exact cause of sarcoidosis, including cardiac sarcoidosis, is not well understood. However, it is believed to involve:
- Immune System Dysfunction: An abnormal immune response triggers the formation of granulomas.
- Genetic Factors: Certain genetic predispositions may make some individuals more susceptible.
- Environmental Factors: Exposure to certain environmental factors, such as infections or toxins, might trigger the condition.
What are the symptoms of cardiac sarcoidosis?
Symptoms of cardiac sarcoidosis can vary depending on the extent of heart involvement and may include:
- Shortness of Breath: Especially with exertion or lying flat.
- Chest Pain: Discomfort or pain in the chest.
- Palpitations: Irregular or rapid heartbeats.
- Fatigue: Extreme tiredness or weakness.
- Syncope: Fainting or near-fainting episodes.
- Swelling: In the legs, ankles, or feet (edema).
How is cardiac sarcoidosis diagnosed?
Diagnosis of cardiac sarcoidosis involves several steps:
- Medical History and Physical Examination: Review of symptoms and overall health.
- Electrocardiogram (ECG or EKG): To detect abnormalities in heart rhythm.
- Echocardiogram: An ultrasound of the heart to assess heart function and structure.
- Cardiac MRI: For detailed imaging of the heart to detect inflammation and scarring.
- Positron Emission Tomography (PET) Scan: To identify active inflammation and granulomas in the heart.
- Endomyocardial Biopsy: A biopsy of the heart tissue to confirm the presence of granulomas (though it may not always be conclusive).
What is the treatment for cardiac sarcoidosis?
Treatment for cardiac sarcoidosis aims to manage symptoms, reduce inflammation, and prevent complications:
- Medications:
- Corticosteroids: Such as prednisone, to reduce inflammation and granuloma formation.
- Immunosuppressants: In cases where corticosteroids are not sufficient or are not well-tolerated.
- Antiarrhythmics: To manage abnormal heart rhythms.
- Lifestyle Modifications: Including a heart-healthy diet, regular exercise, and avoiding alcohol and smoking.
- Device Therapy: Such as implantable cardioverter-defibrillators (ICDs) for those at risk of life-threatening arrhythmias.
- Monitoring and Follow-up: Regular check-ups with a cardiologist to monitor heart function and adjust treatment.