A man in his 60s complained of lower leg edema and exertional dyspnea on Y-8 months, 20XX. He visited a former doctor on Y-4 months, 20XX because of worsening symptoms. He was diagnosed with heart failure and treated with medications. He was referred to our Department of Cardiology on Y month, 20XX because his symptoms persisted. He was scheduled to undergo examinations on an outpatient basis, but he complained of dyspnea, abdominal pain, and diarrhea and underwent emergency hospitalization. Although it was difficult to determine the cause of gastrointestinal symptoms in the emergency department, bradycardia and hypotension persisted. He was admitted and underwent temporary pacemaker implantation. A permanent pacemaker was implanted for sick sinus syndrome on the 4th hospital day. On the 6th hospital day, echocardiography showed a left ventricular ejection fraction of 47%, diastolic dysfunction, bi-ventricular hypertrophy, epicardial brightness and thickening, as well as apical sparing on longitudinal strain. Cardiac amyloidosis was suspected based on these findings. Upper and lower gastrointestinal endoscopy revealed erosion in the stomach and large intestine. Biopsy showed amyloid deposits, and immunostaining revealed the ALκ type. Based on these findings, systemic AL amyloidosis was diagnosed. Although medications were started, the symptoms of heart failure persisted, and cardiac arrest and death occurred on the 48th hospital day. An autopsy was performed to evaluate the pathology of the underlying diseases, and amyloid was found to be deposited in multiple organs including the heart, gastrointestinal tract, lungs, and kidneys. It was diffusely deposited in myocardial tissue and unevenly deposited in the epicardium in a way that penetrated adipose tissue. Amyloid deposits in myocardial tissue are common, but cases with amyloid deposits found in the epicardium are rare, and given that the possibility of this was suggested by echocardiography before death, we report this case with a review of the literature.
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