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Published on: August 8, 2022
Catastrophic cardiac amyloidosis
Prashanth Panduranga1, Mohammed Mukhaini
1Department of Cardiology, Royal Hospital, P.O. Box 1331, Muscat 111, Oman.
Insights
This case highlights that cardiac amyloidosis can cause sudden, severe heart problems. Early recognition is crucial for managing this potentially catastrophic condition.
Area of Science:
- Cardiology
- Cardiovascular Medicine
- Amyloidosis Research
Background:
- Cardiac amyloidosis is a progressive condition often diagnosed late.
- It involves the buildup of amyloid protein in the heart muscle, leading to stiffening and heart failure.
- Acute presentations are less commonly described in the literature.
Observation:
- A 61-year-old male presented with acute cardiogenic shock.
- Echocardiography revealed findings consistent with cardiac amyloidosis.
- The patient's clinical status rapidly deteriorated, indicative of a severe cardiac event.
Findings:
- The echocardiogram showed characteristic features of cardiac amyloidosis, including thickened ventricular walls and diastolic dysfunction.
- The patient's presentation with cardiogenic shock underscores the potential for rapid and severe cardiac compromise.
- This case illustrates a fulminant form of cardiac amyloidosis.
Implications:
- Cardiac amyloidosis requires consideration in the differential diagnosis of acute cardiogenic shock, even in the absence of typical preceding symptoms.
- Prompt diagnosis and management strategies are essential to improve outcomes in patients with acute cardiac amyloidosis.
- This case emphasizes the need for increased awareness among clinicians regarding the acute and catastrophic potential of cardiac amyloidosis.
Abstract:
We report a case of a 61-year-old patient presenting with cardiogenic shock. His echocardiogram suggested typical features of cardiac amyloidosis. This case demonstrates that cardiac amyloidosis can present acutely and may be catastrophic.
Related Concept Videos
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining, normally used to...
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining, normally used to...
