Cardiac amyloidosis presumptively diagnosed as cardiac syndrome X
Atsuhiko Yagishita1, Shuzou Tanimoto, Kengo Tanabe
1Division of Cardiology, Mitsui Memorial Hospital, 1 Kanda-Izumi-cho, Chiyoda-ku, Tokyo, Japan.
Insights
Cardiac amyloidosis can mimic cardiac syndrome X, presenting as angina without significant coronary artery blockages. Autopsy revealed amyloid deposits causing obstruction, leading to heart failure and death.
Area of Science:
- Cardiology
- Pathology
Background:
- Cardiac amyloidosis is a progressive disease that can lead to heart failure.
- Cardiac syndrome X is characterized by angina pectoris with normal coronary arteries.
Observation:
- A 75-year-old man initially diagnosed with cardiac syndrome X presented with worsening angina.
- Despite medical management, his condition progressed to congestive heart failure.
Findings:
- Autopsy revealed amyloid deposits primarily in intramyocardial coronary arteries, causing luminal obstruction.
- Minimal amyloid infiltration was noted in epicardial coronary arteries and myocardium.
Implications:
- This case highlights the importance of considering cardiac amyloidosis in the differential diagnosis of cardiac syndrome X.
- Accurate diagnosis of cardiac amyloidosis is crucial for appropriate management and prognosis.
Abstract:
A 75-year-old man with cardiac amyloidosis was presumptively diagnosed as having cardiac syndrome X. Early clinical presentation was repeated episodes of angina pectoris without angiographically significant stenosis of the coronary arteries, so the diagnosis of cardiac syndrome X was initially given. However, his anginal symptoms worsened despite appropriate medication. He developed congestive heart failure and died 8 years after his first anginal symptoms. Autopsy revealed amyloid deposits in the intramyocardial coronary arteries with luminal obstruction, with little in the epicardial coronary arteries or myocardium. Therefore, the definitive diagnosis was cardiac amyloidosis.
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