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Volume 22, Issue 12, Pages 1327-1334 (December 2009)


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Diastolic Dysfunction and Its Histopathological Correlation in Obstructive Hypertrophic Cardiomyopathy in Children and Adolescents

Shaji C. Menon, MDaCorresponding Author Informationemail address, Benjamin W. Eidem, MDab, Joseph A. Dearani, MDc, Steve R. Ommen, MDb, Michael J. Ackerman, MD, PhDab, Dylan Miller, MDd

published online 08 October 2009.

Refers to corrigendum:
Corrigendum
Journal of the American Society of Echocardiography
February 2010 (Vol. 23, Issue 2, Page 222)
Full Text | Full-Text PDF (36 KB)
Background

Histopathologic hallmarks of hypertrophic cardiomyopathy (HCM) include myocyte hypertrophy and disarray as well as interstitial and endocardial fibrosis. Published correlations between echocardiographic parameters and histopathologic findings are scarce.

Methods

All patients aged <20 years (n = 45; 15 female patients; median age, 14 years) with obstructive HCM undergoing septal myectomy at the Mayo Clinic from 2003 to 2007 were identified. A retrospective review of echocardiographic data was performed, and these data were compared with the histologic findings from the myectomy specimens.

Results

Histopathologic analysis of myectomy specimens revealed significant myocyte hypertrophy (100%), myocyte disarray (98%), interstitial fibrosis (95%), and subendocardial fibrosis (97%). On multivariate regression analysis, there was a significant relationship between the degree of myocyte disarray and echocardiographic markers of left ventricular diastolic dysfunction.

Conclusion

The results of this study suggest that myocyte disarray is a key factor responsible for diastolic dysfunction in pediatric patients with obstructive HCM. These findings provide novel insights into the mechanism of diastolic dysfunction in HCM that warrant further study.

a Department of Pediatric and Adolescent Medicine, Division of Pediatric Cardiology, Mayo Clinic, Rochester, Minnesota

b Department of Medicine, Division of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota

c Department of Surgery, Division of Cardiothoracic Surgery, Mayo Clinic, Rochester, Minnesota

d Department of Laboratory Medicine and Pathology, Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota

Corresponding Author InformationReprint requests: Shaji C. Menon, MD, University of Utah School of Medicine, Division of Pediatric Cardiology, 100 N Mario Capechhi Drive, Salt Lake City, UT 84113.

PII: S0894-7317(09)00766-4

doi:10.1016/j.echo.2009.08.014


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