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Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
A Case of ST-elevated myocardial infarction resulting from obstructive intramural coronary amyloidosis
Katsura Soma1, Masataka Takizawa, Hiroki Uozumi
1Department of Cardiovascular Medicine, Japanese Red Cross Medical Center, Shibuya-ku, Tokyo, Japan.
Insights
Early cardiac amyloidosis can cause acute coronary syndrome by affecting small coronary arteries, even without significant blockages in larger ones. This condition, AL amyloidosis, highlights the need to consider cardiac amyloidosis in acute myocardial infarction cases.
Area of Science:
- Cardiology
- Nephrology
- Hematology
Background:
- Acute coronary syndrome (ACS) is a leading cause of mortality worldwide.
- AL amyloidosis is a systemic disease caused by immunoglobulin light chain deposition.
- Cardiac involvement in AL amyloidosis can lead to various cardiovascular complications.
Observation:
- A 49-year-old man presented with ST-elevated myocardial infarction (STEMI) and diagnosed AL amyloidosis.
- Coronary angiography revealed normal epicardial arteries but abnormal responses to acetylcholine and papaverine, indicating endothelial dysfunction.
- Myocardial biopsy confirmed amyloid deposition solely within the intramural coronary arteries.
Findings:
- Early-stage cardiac amyloidosis, even without significant myocardial infiltration, can precipitate ACS.
- The mechanism involves a combination of epicardial coronary artery spasm and intramural coronary artery obstruction due to amyloid deposits.
- Impaired vascular endothelial function is a key contributor to the ischemic events.
Implications:
- Cardiac amyloidosis should be considered in the differential diagnosis of ACS, particularly in patients with unexplained coronary artery abnormalities.
- Early recognition and management of cardiac amyloidosis may improve outcomes for patients presenting with acute coronary syndromes.
- This case highlights the importance of investigating underlying systemic diseases in patients with myocardial infarction.
Abstract:
A 49-year-old man presenting with ST-elevated myocardial infarction was brought to our emergency department with AL amyloidosis. Baseline coronary angiography showed no significant stenosis of the epicardial coronary arteries, however, coronary artery angiography in response to acetylcholine and coronary flow reserve in response to papaverine were abnormal, which suggested impairment of vascular endothelial function. Myocardial biopsy revealed amyloid deposition exclusively in intramural coronary arteries. Early amyloidosis without myocardial involvement can produce acute coronary syndrome through the combination of spastic epicardial coronary arteries and obstruction of the intramural coronary arteries. In the management of certain patients with acute coronary syndrome, the possibility of cardiac amyliodosis should be taken into consideration.
Related Concept Videos
Acute Coronary Syndrome I: Introduction
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations
Myocarditis I: Introduction
Acute Coronary Syndrome III: Diagnostic Studies
Myocarditis II: Clinical Features and Diagnostic Tests
Cardiomyopathy IV: Restrictive Cardiomyopathy
