Cardiologia Croatica, Vol. 8 No. 3-4, 2013.
Ostalo
Apical hypertrophic cardiomyopathy: a case report.
Stanko Biočić
; Klinička bolnica Dubrava, Zagreb, Hrvatska
Josip Vincelj
; Klinička bolnica Dubrava, Zagreb, Hrvatska
Željko Đurašević
; Klinička bolnica Dubrava, Zagreb, Hrvatska
Diana Rudan
; Klinička bolnica Dubrava, Zagreb, Hrvatska
Sažetak
Apical hypertrophic cardiomyopathy (AHC) is a rare variant of hypertrophic cardiomyopathy characterized by thickening of the most distal part of the left ventricular (LV) wall. It was first described by Sakamoto in 1976 in Japanese patients. AHC was reported as a stri- king electrocardiographic pattern of giant negative T-waves and angiographic feature of end diastolic LV cavity configuration resembling an ace of spade by Yamaguchi et al. Although AHC is more common in Asia and it accounts for about 13% to 25% of all cases of hypertrophic cardiomyopathy, it is much less prevalent in the western population. Diagnostic modalities include ECG, echocardiography, ventriculography, nuclear myocardial perfusion studies and cardiac magnetic resonance imaging.
We present a 58-year-old man with AHC that was unre- cognized for the previous 10 years. In conclusion, this rare disease could be found in the Croatian population too, whereas the appropriate interpretation of the ECG and echocardiography is crucial in recognizing this rare, but important form of hypertrophic cardiomyopathy.
Ključne riječi
apical hypertrophic cardiomyopathy; abnormal ECG; echocardiography
Hrčak ID:
105279
URI
Datum izdavanja:
21.3.2013.
Posjeta: 1.718 *