sarcoidosis

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a chronic disease of unknown cause marked by the formation of nodules in the lungs and liver and lymph glands and salivary glands

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The endomyocardial biopsy is achieved via right heart catheterization and is the gold standard for the diagnosis of cardiac sarcoidosis. The aim is to demonstrate non-caseating granulomas within the myocardium.
For instance, an argument against pure immune dysregulation or autoimmunity is that cardiac sarcoidosis is known to recur in recipients of heart transplants despite the allograft likely having different immunogenic antigens.
Heterogeneity of myocardial 2-[18F]fluoro-2-deoxy-Dglucose uptake is a typical feature in cardiac sarcoidosis: a study of 231 patients.
For each test, the data were classified as positive or negative for the cardiac magnetic resonance imaging detection of cardiac sarcoidosis and sensitivity and specificity estimates were calculated.
He was diagnosed with cardiac sarcoidosis three months after initial presentation.
Regarding cardiac disease, it plays an important role in examining inflammatory disease including acute myocarditis, cardiac sarcoidosis, and cardiac amyloidosis [1-3].
Enokawa et al., "A rare case of cardiac sarcoidosis in a patient with progressive systemic sclerosis, Sjogren's syndrome, and polymyositis," Internal Medicine, vol.
Cardiac sarcoidosis (CS) is clinically present in about 5% of patients, although an autopsy study showed a prevalence of cardiac involvement in approximately 25% of cases [56] which portends worse prognosis [57].
For instance, the 2014 Heart Rhythm Society (HRS) Expert Consensus Statement on the Diagnosis and Management of Arrhythmias Associated with Cardiac Sarcoidosis follows the American College of Cardiology (ACC)/American Heart Association (AHA) Classification of Recommendation and Level of Evidence grading scheme for developing recommendations.[sup][9] Since cardiac sarcoidosis is a rare condition, no randomized (Level A) or nonrandomized studies (Level B) are available, and thus, all recommendations of this consensus statement are given Level C of evidence (based on expert opinion, case studies).
(4) Historically, GCM and cardiac sarcoidosis were often conflated, as both presented in similarly aged patients and could result in a myocarditis characterized by giant cells and granulomas.
Other various causes include cardiomyopathy, myocarditis, trauma, cardiac sarcoidosis, or Chagas disease (3).
Table 1: Two Diagnostic Pathways for Establishing Cardiac Sarcoidosis (CS) (8-9) 1.
Furthermore colchicine mobilizes AY-amyloid and prevents deposition kappa () and lambda () light-chain protein.7-1215 We foresee that aside from cardiac hereditary diseases it might also be a new therapeutic approach in primary amyloidosis cardiac sarcoidosis neurodegenerative and psychiatric disorders such as Alzheimer disease and autism.1015
Magnetic resonance imaging (MRI), while important in the diagnosis of neurological and cardiac sarcoidosis, has little role in the diagnosis of the pulmonary form of the disease.