(Circulation. 2000;102:e71.)
© 2000 American Heart Association, Inc.
Images in Cardiovascular Medicine |
From the Department of Cardiology, Thoraxcenter (R.J.M.v.G., P.J.d.F., S.E.S.) and the Department of Radiology, Dr Daniel den Hoedkliniek, University Hospital Rotterdam (M.O.), Rotterdam, The Netherlands.
Correspondence to Robert J.M. van Geuns, MD, Department of Cardiology, Thoraxcenter, Bd 406, University Hospital Rotterdam, PO Box 2040, 3000 CA Rotterdam, The Netherlands. E-mail vangeuns@card.azr.nl
A19-year-old man with
known dextrocardia, situs inversus, and complete surgical correction of
a double-outlet right ventricle was seen in the outpatient clinic for
follow-up after total correction, including the implantation of a
pulmonary homograft. During
echocardiography, a dilated right atrium and right
ventricle were noted. Increased right ventricular pressure
(50 mm Hg; tricuspid regurgitation, 3.5 m/s)
could only partially be explained by pulmonary valve
stenosis. The pulmonary artery branches could not be
visualized echocardiographically. Magnetic resonance
angiography was performed using the breath-hold contrast-enhanced 3D
gradient echo sequence described by Prince et al.1 The
imaging time was 24 seconds and the resolution was 1.0x2.6x1.3
mm. After the acquisition, the datasets were transferred to a dedicated
graphic workstation (Indigo2, Silicon Graphics) for 3D
evaluation with a volume-rendering technique2 3 using
commercially available software (VoxelView, Vital Images).
Three-dimensional representation with volume rendering showed
the situs inversus very clearly (Figure 1
). The pulmonary homograft is
located on the right side of the patient, with the ascending aorta on
the left and descending aorta to the right of the spine. The branch
vessels are reversed, with a left brachiocephalic artery as the first
arch branch.
|
To visualize the pulmonary artery branches, the heart and aorta
were subtracted from the source images (Figure
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