(Circulation. 2003;108:e136.)
© 2003 American Heart Association, Inc.
Images in Cardiovascular Medicine |
From the Department of Cardiology, St Lukes Episcopal Hospital, Texas Heart Institute, Houston, Tex.
Correspondence to Raymond F. Stainback, MD, Department of Cardiology, St Lukes Episcopal Hospital, 6720 Bertner Ave, MC 1-133, Houston, TX 77030. E-mail rstainback@sleh.com
An extract of the first 100% of the full text is provided, because this article has no abstract. |
A 21-year-old man presented with syncope and a heart murmur. Screening echocardiography revealed severe asymmetric septal hypertrophic cardiomyopathy (thickness, 3.7 cm). No resting or provocable left ventricular outflow obstruction was present. Because the patient was not an athlete and performed no regular strenuous physical activity, medical therapy with ß-blockers was prescribed. Subsequently, the patient remained asymptomatic but became extremely dependent on the medical therapy. Even one missed dose would lead to presyncopal episodes. On follow-up at 23 years of age, echocardiography revealed extreme septal hypertrophy (thickness, 4.2 cm) (Movies I and II; see Data Supplement). A cardioverter-defibrillator was implanted.
In this patient, the relatively rapid progression of severe hypertrophic cardiomyopathy to extreme septal hypertrophy and the consequent potential increase in risk of sudden death was believed to necessitate placement of an implantable cardioverter-defibrillator.
Movies I and II are available in an online-only Data Supplement at http://www.circulationaha.org.
The editor of Images in Cardiovascular Medicine is Hugh A. McAllister, Jr, MD, Chief, Department of Pathology, St Lukes Episcopal Hospital and Texas Heart Institute, and Clinical Professor of Pathology, University of Texas Medical School and Baylor College of Medicine.
Circulation encourages readers to submit cardiovascular images to the Circulation Editorial Office, St Lukes Episcopal Hospital/Texas Heart Institute, 6720 Bertner Ave, MC1-267, Houston, TX 77030.
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