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Case Reports
. 2008 Aug;63(4):557-60.
doi: 10.1590/s1807-59322008000400026.

A case of pseudo-hypertrophic cardiomyopathy: a congenital heart disease

Riccardo Ieva, Michele Correale, Matteo Di Biase
Case Reports

A case of pseudo-hypertrophic cardiomyopathy: a congenital heart disease

Riccardo Ieva et al. Clinics (Sao Paulo). 2008 Aug.
No abstract available

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Figures

Figure 1
Figure 1
Detail of the three-leaflet tricuspid valve
Figure 2
Figure 2
Apical four-chamber view shows dilatation of both the left atrium and left appendage and a smooth interventricular septalright surface against the trabeculated septal left surface in the correct position (normal atrial situs). This permits diagnosis of ventricular inversion and the presence of a three-leaflet tricuspid valve inserted more apically than the mitral valve
Figure 3
Figure 3
The pulmonary trunk, identified by its bifurcation
Figure 4
Figure 4
Details of the systemic ventricle apical segments with prominent trabeculations and color flow imaging. This analysis reveals forward and reverse flow between trabeculae during the cardiac cycle
Figure 5
Figure 5
Transesophageal examination shows the morphological features of the appendage
Figure 6
Figure 6
In prominent systemic ventricle hypertrophy, the aortic valve and the systemic atrioventricular valve are discontinuous because of muscle interposition
See this image and copyright information in PMC

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