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Potential novel imaging targets of inflammation in cardiac sarcoidosis.
Park, Jakob; Young, Bryan D; Miller, Edward J.
Affiliation
  • Park J; Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
  • Young BD; Section of Cardiovascular Medicine, Department of Medicine, Yale School of Medicine, 333 Cedar Street, New Haven, CT, 06520, USA.
  • Miller EJ; Section of Cardiovascular Medicine, Department of Medicine, Yale School of Medicine, 333 Cedar Street, New Haven, CT, 06520, USA. edward.miller@yale.edu.
J Nucl Cardiol ; 29(5): 2171-2187, 2022 Oct.
Article in En | MEDLINE | ID: mdl-34734365
ABSTRACT
Cardiac sarcoidosis (CS) is an inflammatory disease with high morbidity and mortality, with a pathognomonic feature of non-caseating granulomatous inflammation. While 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) is a well-established modality to image inflammation and diagnose CS, there are limitations to its specificity and reproducibility. Imaging focused on the molecular processes of inflammation including the receptors and cellular microenvironments present in sarcoid granulomas provides opportunities to improve upon FDG-PET imaging for CS. This review will highlight the current limitations of FDG-PET imaging for CS while discussing emerging new nuclear imaging molecular targets for the imaging of cardiac sarcoidosis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoidosis / Cardiomyopathies / Myocarditis Limits: Humans Language: En Journal: J Nucl Cardiol Journal subject: CARDIOLOGIA Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoidosis / Cardiomyopathies / Myocarditis Limits: Humans Language: En Journal: J Nucl Cardiol Journal subject: CARDIOLOGIA Year: 2022 Type: Article Affiliation country: United States