Abstract

A 61 year-old man presented orthopnea in 2004. A echocardiography revealed severe reduction of left ventricle (LV) ejection fraction of 27% and dilation of LV end-dyastoric dimension of 65 mm with posterior wall thinning. There were no specific lung, skin or eye findings suspicious of sarcoidosis. Endomyocardial biopsy also showed no specific findings. Therefore, he was diagnosed and treated as dilated cardiomyopathy. However, the condition of heart failure progressively deteriorated and became refractory. He was hospitalized in March 2017 due to the worsening of heart failure. He was treated with inotropes, because he presented anorexia caused by low cardiac output. During the hospitalization, electrical defibrillation was needed because of the sustained ventricular tachycardia. Under the treatment of inotropes, his pulmonary capillary wedge pressure and cardiac index were 28 mmHg and 1.9 L⋅min−1⋅m−2, respectively. Therefore, we were introduced intra-aortic balloon pumping and planned to register him for heart transplantation. We performed 18-fluorodeoxyglucose (FDG) positron emission tomography for the role out of sarcoidosis, and it showed intense uptake of FDG in diffuse myocardium. Therefore, we finally diagnosed him as cardiac sarcoidosis. We introduced steroid therapy, and heart failure symptoms were improved, after then IABP was successfully weaned.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.