This case report illustrates challenging aspects of diagnosis of isolated cardiac
sarcoidosis. Here, we present a 69-year-old female who had been diagnosed as dilated
cardiomyopathy before was admitted to our hospital for congestive heart failure. Coronary
angiography showed no significant abnormalities. Left ventriculography revealed left
ventricular aneurysm. The endomyocardial biopsy specimens showed no significant findings.
Cardiac MRI showed late enhancement at the lateral wall of the left ventricle, this
finding suggested the presence of cardiac sarcoidosis. However, Ga citrate scintigraphy
and examination of eyes showed no signs of extracardiac sarcoidosis and pulmonary
sarcoidosis was excluded by chest CT. Therefore, she did not fulfill the diagnostic
criteria for cardiac sarcoidosis. Since then her symptoms gradually worsened and she
was readmitted to our hospital for recurrent heart failure in April 2017. During hospitalization,
she developed monomorphic sustained ventricular tachycardia. Thus, she met the diagnostic
criteria for possible isolated cardiac sarcoidosis. Steroid immunosuppressive therapy
was started at this time. Catheter radiofrequency ablation was performed on the 21st
hospital day and cardiac resynchronization therapy defibrillator was implanted at
a later date. We report a case of possible isolated cardiac sarcoidosis presenting
difficulty in diagnosis, mimicking idiopathic dilated cardiomyopathy.
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