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2040-01-01
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- INI - Artigos de Periódicos [3393]
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CAN PET/CT BE USEFUL IN PREDICTING VENTRICULAR ARRHYTHMIAS IN CHAGAS DISEASE?
Author
Affilliation
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Rio de Janeiro, RJ, Brasil / D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Rio de Janeiro, RJ, Brasil / D'Or Institute for Research and Education. Rio de Janeiro, RJ, Brazil.
Abstract
Ventricular arrhythmias are a major cause of morbidity and mortality in patients with Chagas disease and
may occur even before significant left ventricular (LV)
systolic dysfunction. Cardiac Chagas disease is characterized by chronic persistent myocardial inflammation,
which plays a central role in the genesis of arrhythmias
due to irreversible cell damage and scar formation. In
addition, active inflammation may increase the automaticity within inflamed areas, or act as a trigger for reentry in the presence of fibrosis. Case Summary: A 68-year-old man presented with an episode of
sustained ventricular tachycardia associated to cardiac
Chagas disease with ischemic changes on ECG, moderate
LV dysfunction and an apical aneurysm on echocardiography. Cardiac magnetic resonance (CMR) imaging
showed apical aneurysm and inferolateral late gadolinium enhancement (LGE). Fluorine-18-labeled 2-deoxy-
2-fluoro-D-glucose (18F-FDG) positron emission tomography (PET)/computed tomography (CT) and 68-labeled gallium-DOTA-tyr3-Octreotide (68Ga-DOTATOC)
PET/CT revealed increased uptake adjacent to hypoperfused or fibrotic areas.
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