Key result
Corticosteroids rapidly improve clinical and imaging findings in a case of tumor-like isolated cardiac sarcoidosis.
Case Report (n=1)
Isolated cardiac sarcoidosis can present as tumor-like masses mimicking malignancy, highlighting the importance of multimodality imaging and histological confirmation for accurate diagnosis and management.
Corticosteroids may yield rapid remission in tumor-mimicking cardiac sarcoidosis; leaves open need for prospective trials before routine adoption.
A 30-year-old man presented with progressive dysphagia and palpitations. Electrocardiography showed first-degree atrioventricular block. Imaging revealed massive pericardial effusion and tumor-like intracardiac masses involving the aortic root and interatrial septum. Cardiac tamponade required drainage. FDG-PET demonstrated uptake confined to the heart, and cardiac magnetic resonance showed myocardial edema with limited late gadolinium enhancement. Endomyocardial biopsy revealed non-caseating granulomas, establishing the diagnosis of isolated cardiac sarcoidosis. Corticosteroid therapy led to rapid clinical and imaging improvement. This case illustrates that isolated cardiac sarcoidosis can mimic malignancy and requires multimodality imaging with histological confirmation.
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Yamada et al. (2026) conducted a case report in Isolated cardiac sarcoidosis (n=1). Corticosteroid therapy was evaluated on Clinical and imaging improvement. Corticosteroid therapy led to rapid clinical and imaging improvement in a 30-year-old man with isolated cardiac sarcoidosis presenting as tumor-like cardiac masses.
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