Rare Occurrence of Apical Hypertrophic Cardiomyopathy Among Hispanics
Case Reports
. 2022 Dec;13(6):393-397.
doi: 10.14740/cr1437.
Epub 2022 Dec 1.
Affiliations
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Case Reports
Cardiol Res.
2022 Dec.
Abstract
Apical hypertrophic cardiomyopathy (ApHCM), also known as Yamaguchi syndrome represents an uncommon morphologic variant of hypertrophic cardiomyopathy (HCM) in which the myocardial hypertrophy predominantly involves the apex of the left ventricle (LV). It is exemplified by “giant” negative precordial T-waves on electrocardiography and a peculiar “spade-like” configuration of LV cavity on ventriculography historically, and more recently, on echocardiography with use of image enhancing agents. The disease entity was first described in 1976. Available literature reveals that it is prevalent largely among the East-Asian population but is rare among non-Asians. Here, we report a case of a 66-year-old Hispanic male with multiple cardiac histories including persistent atrial fibrillation, non-ST-elevation myocardial infarction (NSTEMI), and ventricular fibrillation cardiac arrest with multiple inconclusive evaluations, who later in life was found to have ApHCM. This case highlights the rare incidence of the disease among the Hispanic population and underlines the challenging diagnosis that requires a high index of suspicion in patients with cardiac symptoms, as ApHCM can masquerade as ischemic coronary heart disease. Our case also describes an unusual clinical course for ApHCM presenting with extreme clinical features, including ventricular arrhythmias and cardiac arrest, unlike the usual benign natural history of this disease.
Keywords:
Apical hypertrophic cardiomyopathy; Cardiac arrest; Echocardiogram; Hispanic; Ventricular fibrillation; Yamaguchi syndrome.
Copyright 2022, Abdalla et al.
Conflict of interest statement
There is no conflict of interest in this case report from all authors.
Figures
Figure 1
ECG on presentation shows atrial fibrillation and prominent T-waves inversion in leads V3 through V6. ECG: electrocardiogram.

Figure 2
ECG about 1 year prior to presentation shows normal sinus rhythm and prominent T-waves inversion in leads V3 through V6. ECG: electrocardiogram.

Figure 3
(a) Echocardiogram without contrast during diastole. (b) Echocardiogram without contrast during systole. (c) Echocardiogram with contrast during diastole showing the spade like ventricular cavity. (d) Echocardiogram with contrast during systole.
References
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Kureshi SA, Malik SM, Hyder W. Apical hypertrophic cardiomyopathy in Pakistan: electrocardiographic, echocardiographic and myocardial scintigraphic features. J Pak Med Assoc. 1995;45(5):117–120.
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PubMed
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