becoming a better Clinician
Cardiac Sarcoid
last updated: November 4, 2016
Orlando Debesa
Cardiac Sarcoid
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heterogeneous, non-caseating, granulomatous disorder of unknown etiology (maybe environmental, occupational, infectious triggers)
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geographic variations
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Japan cardiac involvement 50-75%
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US cardiac involvement 15-50%
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clinical manifestations
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conduction blocks
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tachyarrhythmias
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cardiomyopathy
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heart failure (especially in the young, middle aged)
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sudden cardiac death
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mitral incompetence
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due to associated systolic dysfunction and left ventricular dilation
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granuloma on papillary muscle
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can be severe enough to cause pulmonary hypertension requiring mitral valve replacement
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tricuspid regurgitation with AV block secondary to infiltration has been reported
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Treatment
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glucocorticoids
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immunomodulating (steroid sparing) agents
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pacing / ICD
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ablation
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transplant
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