Abstract
Differential diagnosis of asymmetrical left ventricular hypertrophy may be challenging, particularly in patients with history of hypertension. A middle-aged man underwent an echocardiographic examination during workup for hypertension, which unexpectedly showed significant asymmetrical septal hypertrophy and raised suspicion for hypertrophic cardiomyopathy. Cardiovascular magnetic resonance confirmed the asymmetrical hypertrophy. No myocardial late gadolinium contrast enhancement was seen. However, precontrast T1 mapping revealed a low native myocardial T1 value. This was highly suggestive of Anderson-Fabry disease, which was subsequently proved with very low alpha galactosidase enzyme levels and mutation analysis. The case illustrates clinical usefulness of multimodality imaging and the novel tissue characterization techniques for assessment of left ventricular hypertrophy.
Original language | English |
---|---|
Pages (from-to) | 1765-1768 |
Number of pages | 4 |
Journal | Echocardiography |
Volume | 33 |
Issue number | 11 |
Early online date | 10 Sep 2016 |
DOIs | |
Publication status | Published - Nov 2016 |
Keywords
- Anderson-Fabry disease
- cardiac magnetic resonance imaging
- echocardiography
- hypertrophic cardiomyopathy
- left ventricular hypertrophy