Isolated cardiac sarcoidosis: A systematic review
Shokoufeh Hajsadeghi1, Elham Piryaie2, Shayan Mirshafiee3
1Research Center for Prevention of Cardiovascular Disease, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Iran.
Isolated cardiac sarcoidosis, a heart-exclusive condition, affects men and women equally. This understudied disease presents a poorer prognosis than multi-organ sarcoidosis, necessitating further research.
Area of Science:
- Cardiology
- Immunology
- Rare Diseases
Background:
- Isolated cardiac sarcoidosis is a rare condition affecting only the heart.
- It can lead to severe complications like arrhythmias and heart failure.
- This specific entity remains understudied, lacking systematic reviews.
Purpose of the Study:
- To systematically review the existing literature on isolated cardiac sarcoidosis.
- To characterize the epidemiology, clinical presentation, and outcomes of this condition.
- To identify gaps in knowledge and areas for future research.
Main Methods:
- A systematic literature search was conducted from 1978 to 2025.
- 14 relevant studies, predominantly case series, were included.
- Data on patient demographics, clinical features, and outcomes were extracted and analyzed.
Main Results:
- The condition affects both sexes equally, typically in patients aged 55-65 years.
- Isolated cardiac sarcoidosis is linked to reduced left ventricular ejection fraction and worse survival compared to multi-organ disease.
- Diagnostic criteria variability and potential selection bias were noted limitations.
Conclusions:
- Isolated cardiac sarcoidosis is a distinct and severe clinical entity with limited data.
- Its poorer prognosis highlights the need for specific diagnostic and management guidelines.
- Multicenter studies are crucial for advancing understanding and patient care.
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