(Circulation. 2001;103:e89.)
© 2001 American Heart Association, Inc.
Correspondence |
Bnai-Zion Medical Center, Medical Faculty, Technion, Golomb Street 47, Haifa, Israel
To the Editor:
We read with interest the findings reported by Gruberg et al.1 At 33 years of age, the patient had left ventricular hypertrophy by echocardiography and, in the absence of obvious reasons for hypertrophy, the diagnosis of hypertrophic cardiomyopathy (HCM) should be considered. The electrocardiographic changes and the spade-like appearance of the left ventricle at angiography (Figure 3) support the diagnosis of apical HCM. Furthermore, the authors report a normal ventriculogram at 33 years, thus excluding the diagnosis of a congenital defect and supporting acquired disease diagnosed 16 years later at the age of 49 years.
We reported on a patient with apical HCM2 who, at long-term follow-up, had attenuation of the amplitude of the R waves and reduced negativity of the giant precordial T waves associated with progressive development of apical left ventricular aneurysm and normal coronary angiogram.
Thus, the findings reported by the authors favor the diagnosis of apical HCM with progressive remodelling of the left ventricular apex, rather than a congenital defect in the form of Cantrells syndrome.
References
1.
Gruberg L,
Goldstein SA, Pfister AJ, et al. Cantrells syndrome: left
ventricular diverticulum in an adult patient.
Circulation. 2000;101:109110.
2. Abinader EG, Rauchfleisch S, Naschitz J. Hypertrophic apical cardiomyopathy: a subtype of hypertrophic cardiomyopathy. Israel J Med Sci. 1982;18:10051009. \.[Medline] [Order article via Infotrieve]
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