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Circulation. 2006;113:e458-e459
doi: 10.1161/CIRCULATIONAHA.105.559948
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(Circulation. 2006;113:e458-e459.)
© 2006 American Heart Association, Inc.


Images in Cardiovascular Medicine

Hereditary Hypertrophic Nonobstructive Cardiomyopathy Seen on Delayed Hyperenhancement Magnetic Resonance Imaging

Henning Steen, MD; Philipp Ehlermann, MD; Constanze Merten, MD; Philipp Schnabel, MD; Matthias Lutz, MD; Evangelos Giannitsis, MD; Hugo A. Katus, MD

From the Division of Cardiology, Pneumology, and Angiology, Department of Internal Medicine III, University of Heidelberg, Germany.

Correspondence to Hugo A. Katus, MD, Division of Cardiology, Pneumology, and Angiology, Department of Internal Medicine III, University of Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany. E-mail Sekretariat_Katus{at}med.uni-heidelberg.de

A 25-year-old professional handball player collapsed in the team bus and was resuscitated. Afterward, he was presented to our clinic for further cardiac examination. During the electrophysiological study and at myocardial biopsy, ventricular fibrillation was induced and electrophysiologically reterminated. Magnetic resonance cine imaging (Figure, A; see also Movie I) showed good left ventricular (LV) function and a thickened, 28-mm, predominantly anterior LV wall without intraventricular flow turbulence. Pronounced delayed hyperenhancement (Figure, B, arrow) was observed after gadolinium exposition within hypertrophied muscle areas. Histology (hematoxylin and eosin stain; Figure, C) revealed myocardial disarray of muscular fibers and pronounced fibrosis generally common in hypertrophic cardiomyopathies. During left heart catheterization, no intraventricular pressure gradient was measured. Therefore, having come to the diagnosis of hypertrophic nonobstructive cardiomyopathy, we implanted a defibrillator. On inquiry, the father of the patient agreed to undergo cardiac magnetic resonance imaging (MRI) (although he had reported no cardiac symptoms), a normal treadmill test, and a 24-hour Holter ECG, with only insignificant findings. Although he displayed no clinical symptoms, he—like his son—showed a good ventricular function in steady-state free precession MRI (Figure, D; see also Movie II), with even more pronounced delayed hyperenhancement in his hypertrophied LV but more septal affected areas (Figure, E, arrow). MRI provides invaluable tissue information and demonstrates conclusively its importance as a diagnostic tool in familial cardiomyopathy studies. Simultaneously, the MRI results raise the question of therapy for family members with identical appearance on MRI scans but without clinical symptoms.


Figure 1
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Left ventricular (LV) short-axis MRI (A and D) and corresponding delayed hyperenhancement images (B and E) of son (upper panel) and father (lower panel). Histology of the son’s myocardium (C, hematoxylin and eosin stain) showed myocardial disarray of muscular fibers and pronounced fibrosis.


*    Acknowledgments
 
Disclosures

None.


*    Footnotes
 
The online-only Data Supplement can be found at http://circ.ahajournals.org/cgi/content/full/113/11/e458/DC1.


Related Article:

Issue Highlights
Circulation 2006 113: 1377. [Full Text]




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*Compound via MeSH
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*Cardiomyopathy
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Right arrow Contractile function
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Right arrow CT and MRI
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