(Circulation. 2001;103:e39.)
© 2001 American Heart Association, Inc.
Images in Cardiovascular Medicine |
From the Department of Pediatrics, Division of Cardiology, and the Variety Club Cardiac Catheterization Laboratories, The Hospital for Sick Children, University of Toronto School of Medicine, Toronto, Ontario, Canada.
A female child with visceral heterotaxy (presumed left isomerism), interrupted inferior vena cava with azygos continuation to the superior vena cava, and double-outlet right ventricle underwent a total cavopulmonary anastomosis (end-to-side anastomosis of the superior vena cava to the right pulmonary artery) in infancy. Completion of Fontan circulation was undertaken at 3 years of age with construction of a tunnel from the hepatic veins to the pulmonary artery confluence.
By 6 years of age, the child had become increasingly
cyanotic, and cardiac catheterization was performed to define the
mechanism of the cyanosis.
Figure 1
is a pulmonary artery angiogram that reveals
moderate hypoplasia of the pulmonary artery confluence.
Figure 2
is a selective angiogram performed in the hepatic
vein tunnel, with hepatic venous flow directed predominantly toward the
left lung. The left pulmonary artery angiogram was normal. A right
pulmonary artery angiogram
(Figure 3
) was markedly abnormal, showing a diffusely
granular appearance of the distal vasculature and early appearance of
contrast in the right pulmonary veins, characteristic of the presence
of pulmonary arteriovenous malformations. The development of
arteriovenous malformations in the right lung allowed for
intrapulmonary right-to-left shunting, accounting for the patients
progressive cyanosis.
Figure 4
is an azygos vein angiogram, performed after the
implantation of an intravascular stent into the hypoplastic pulmonary
artery confluence. Note the presence of a duplicated inferior vena cava
(the left inferior vena cava received the left renal vein).
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