AJR 2000; 174:125-131
© American Roentgen Ray Society
Spontaneous Intrahepatic Vascular Shunts
Michael J. Lane1,
R. Brooke Jeffrey, Jr.2 and
Douglas S. Katz3
1
Department of Radiology, Brooke Army Medical Center, 3851 Roger Brooke Dr.,
Ft. Sam Houston, San Antonio, TX 78234.
2
Department of Radiology, Stanford University Medical Center, 300 Pasteur Dr.,
Stanford, CA 94305.
3
Department of Radiology, Winthrop University Hospital, 259 First St., Mineola,
NY 11501.
Received March 1, 1999;
accepted after revision June 9, 1999.
Address correspondence to M. J. Lane.
Introduction
Multiphase helical CT and multiphase dynamic MR imaging represent advances
in cross-sectional imaging that allow evaluation of the liver during arterial
and portal venous phases of contrast enhancement. A recent article describes
perfusion disorders of the liver as manifestations of increased attenuation
[1]. However, abnormal
communication between the hepatic arteries, portal veins, or hepatic veins
have been described in relatively few reports. Although communication within
the liver between the hepatic artery and portal vein has been reported,
including transsinusoidal, transvasal, and transplexal routes, these vascular
communications are typically small and below the threshold of visualization
with cross-sectional imaging
[2].
The frequency in which large intrahepatic vascular shunts are visualized on
cross-sectional imaging is unknown. Large shunts may appear as hypervascular
lesions and may occasionally simulate primary neoplasms of the liver.
Recognition of large shunts can provide insight into the patient's
pathophysiology, especially in cirrhosis and portal hypertension. This
pictorial essay will review conditions associated with known and unknown
abnormalities of large intrahepatic shunts, their appearances on multiphase
contrast-enhanced CT and MR imaging, and their sonographic and angiographic
correlation.
Three types of intrahepatic shunts between the major vessels of the liver
are possible: portosystemic venous (portal vein to hepatic vein or vena cava),
arterioportal (hepatic artery to portal vein), and arteriosystemic (hepatic
artery to hepatic vein). Visualization of these shunts on cross-sectional
imaging is unusual. Most shunts, particularly portosystemic shunts, are
identified in the setting of cirrhosis. Intrahepatic portosystemic shunts may
also be congenital or posttraumatic in origin. Arterioportal shunts are
typically associated with hepatocellular carcinoma (HCC), vascular
malformations involving the liver, or benign hepatic neoplasms; they may also
be iatrogenic after biopsy. Recently, idiopathic nontumoral arterioportal
shunts have been researched
[3]. Arteriosystemic
intrahepatic shunts are rare and are typically associated with hepatic
neoplasms.
Portosystemic Venous Shunt
Intrahepatic portosystemic (portal to hepatic) venous shunts are uncommon.
Postulated congenital origins of portosystemic shunts include the persistence
of an omphalomesenteric venous system with the right horn of the sinus venosus
or rupture of a portal vein aneurysm into a hepatic vein
[4]. Acquired conditions such
as trauma and portal hypertension are also theorized
[5]. Portosystemic shunts are
typically identified incidentally as part of the workup for cirrhosis or, less
commonly, after a patient's condition is diagnosed as hepatic encephalopathy
[4]
(Fig. 1).

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Fig. 1. 65-year-old man with portosystemic shunt undergoing evaluation for
cirrhosis. Arterial phase CT scan shows direct communication of left portal
vein (curved arrow) and middle hepatic vein (straight
arrow).
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Patients with severe portal hypertension can develop extensive
portosystemic collaterals draining directly into the inferior vena cava by way
of a subcapsular route [5]
(Fig. 2A,
Fig. 2B). Sonography can
identify the communication between the portal vein and the hepatic or systemic
veins (Fig. 3A,
Fig. 3B, Fig. 3C,
Fig. 3D).

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Fig. 2. 58-year-old woman with hepatic encephalopathy and portosystemic
shunt.
A, Contrast-enhanced CT scan shows dilated right portal vein
(curved arrow) and large subcapsular systemic vein (straight
arrow) emptying into inferior vena cava. Note splenic infarcts, splenic
artery aneurysm (A), and bilateral pleural effusions.
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Fig. 2. 58-year-old woman with hepatic encephalopathy and portosystemic
shunt.
B, Contrast-enhanced CT scan caudal to A shows dilated right
portal vein communicating with large subcapsular systemic vein (curved
arrow).
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Fig. 3. 47-year-old man with portosystemic shunt undergoing evaluation for
cirrhosis.
B, Contrast-enhanced portal venous-phase CT scan shows aneurysmal
site of communication (curved arrow) between right portal vein and
right hepatic vein.
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Fig. 3. 47-year-old man with portosystemic shunt undergoing evaluation for
cirrhosis.
C, Contrast-enhanced portal venous-phase CT scan shows dilated right
hepatic vein (arrow) and normal-appearing middle and left hepatic
veins (arrowheads).
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Fig. 3. 47-year-old man with portosystemic shunt undergoing evaluation for
cirrhosis.
D, Power Doppler sonogram shows direct communication between portal
(straight arrow) and hepatic (curved arrow) veins.
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Arterioportal Shunts
Arterioportal shunts occur in liver disorders such as cirrhosis, trauma,
congenital vascular malformations, and hepatic neoplasms. Arterioportal
shunting associated with cirrhosis or HCC is also well documented
[6]. The degree of shunting is
greater with neoplasms than with cirrhosis and even greater with large tumors.
Research shows that the prevalence of arterioportal shunting in HCC is as high
as 63% of patients [6]. The
hepatic artery supplies HCC almost exclusively, providing the intense early
enhancement seen in arterial phase imaging. The tendency for these neoplasms
to grow in the portal veins causes the venules to act as efferent vessels for
the tumor, establishing the arterioportal shunt. The CT or MR imaging findings
of arterioportal shunting include early and prolonged enhancement of the
portal vein, transient wedge-shaped enhancement peripheral to the tumor (if
one is present), and dilated intrahepatic vessels during arterial phase
imaging [6].
Intrahepatic nontumorous arterioportal shunts can be idiopathic, resulting
from penetrating trauma, or iatrogenic after liver biopsy or percutaneous
catheterization of the bile ducts
[3]. The abnormally enhancing
vein is often enlarged because of the higher systemic pressures presented by
the hepatic artery. Enlarged hepatic arteries may also be seen in the vicinity
of the shunt. Idiopathic intrahepatic nontumoral arterioportal shunts are
typically subcapsular or peripheral as seen angiographically or on arterial
phase helical CT (Fig. 4A,
Fig. 4B). They appear as focal
increased-attenuation wedge-shaped defects with early portal venous filling
[3]. Additionally, small
idiopathic nontumoral arterioportal shunts have been shown to simulate small
hypervascular masses such as HCC, focal nodular hyperplasia, and
hemangiomas.

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Fig. 4. 55 year-old man with elevated liver function tests and arterioportal
shunt.
A, Contrast-enhanced arterial phase CT scan shows wedge-shaped
subcapsular region of increased attenuation (straight arrow). Note
early portal venous filling (curved arrow), representing small
idiopathic nontumoral arterioportal shunt confirmed angiographically (not
shown).
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Infrequently, intrahepatic arterioportal shunts may cause life-threatening
portal hypertension (Fig. 5A,
Fig. 5B,
Fig. 5C,
Fig. 5D). Surgical
intervention is necessary only when interventional radiologic procedures such
as emoblization have failed. The shunt or fistula between the hepatic artery
and the portal vein is rarely visualized on CT.

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Fig. 5. 70-year-old man with hematemesis and arterioportal shunt.
A, Contrast-enhanced arterial phase CT scan shows
cirrhotic-appearing liver. Note dilatation of peripheral hepatic arterial
branch (straight arrow) and dilated right portal vein (curved
arrow).
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Fig. 5. 70-year-old man with hematemesis and arterioportal shunt.
B, Gray-scale sonogram shows dilated hepatic artery branches
(straight arrows) and right portal vein (curved arrow).
Spectral Doppler imaging (not shown) showed arterial waveform in right portal
vein, consistent with arterioportal shunting.
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Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu disease is an
autosomal dominant disorder that may involve virtually every organ and is
reported to involve the liver in 8-31% of patients
[7]. The hepatic manifestations
of this disorder include vascular malformations, cirrhosis, and fibrosis
[7]. Arterioportal or
arteriosystemic venous shunts are also described as manifestations of this
congenital disorder. However, identification of a specific abnormal
communication in the presence of multiple hepatic vascular malformations can
be challenging. The appearance of an early enhancing portal or hepatic vein
during the arterial phase of the CT or MR imaging examination is the clue to
the diagnosis. Color and Doppler sonography can identify the presence of
vascular malformations and the arterioportal or arteriosystemic venous shunts
and their hemodynamic significance. Identifying the arterialized waveform in a
portal vein may help direct angiography to determine the need for embolization
[7]
(Fig. 6A, Fig. 6B,
Fig. 6C,
Fig. 6D).

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Fig. 6. 51-year-old woman with Osler-Weber-Rendu disease and arterioportal
shunt.
A, Contrast-enhanced arterial phase CT scan shows small vascular
malformations throughout liver. Note early filling of dilated left portal vein
(straight arrow) adjacent to dilated left hepatic artery (curved
arrow), suggestive of arterioportal shunt.
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Fig. 6. 51-year-old woman with Osler-Weber-Rendu disease and arterioportal
shunt.
D, Spectral Doppler sonogram (with color assignment change compared
with C) shows arterialized portal venous waveform, confirming
arterioportal shunt.
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Arterioportal shunts are rarely reported in association with hepatic
hemangiomas [8]. The
characteristic appearance of hemangiomas on CT or MR imaging, coupled with the
identification of a dilated feeding artery and early portal venous filling,
should lead to the correct diagnosis. The degree of shunting determines
whether manifestations of portal hypertension are present
[9]
(Fig. 7A,
Fig. 7B,
Fig. 7C,
Fig. 7D,
Fig. 7E, Fig. 7F). When subcapsular,
small hemangiomas may simulate a small arterioportal shunt without a
coexisting lesion. Peripheral wedge-shaped regions of increased perfusion that
become isodense or isointense on delayed images can be seen with small
hemangiomas and arterioportal shunts
[3,
8].

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Fig. 7. 50-year-old man with hematemesis and arterioportal shunt.
A, Contrast-enhanced arterial phase CT scan shows nodular
enhancement (arrow) in low-attenuation lesion near dome of liver.
Lesion filled with contrast material on delayed images (not shown). Ascites is
present.
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Fig. 7. 50-year-old man with hematemesis and arterioportal shunt.
B, Contrast-enhanced arterial phase CT scan caudal to A shows
aneurysmal site of communication between dilated hepatic artery
(arrow) and early contrast enhancement in main portal vein
(arrowhead).
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Fig. 7. 50-year-old man with hematemesis and arterioportal shunt.
C, Contrast-enhanced arterial phase CT scan near porta hepatis shows
cirrhotic-appearing liver, ascites, splenomegaly, dilated tortuous hepatic
artery (straight arrow), and early contrast enhancement of main
portal vein (curved arrow).
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Fig. 7. 50-year-old man with hematemesis and arterioportal shunt.
D, Coronal contrast-enhanced three-dimensional spoiled
gradient-recalled MR angiogram during arterial phase shows dilated hepatic
artery (straight arrow) arising from celiac axis (C). Note early
retrograde filling of main portal vein (curved arrow). Nodular
enhancement of hemangioma (arrowheads) is seen near liver dome.
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Arteriosystemic Shunts
Arteriosystemic shunts involving the liver are rare and are typically
associated with benign and malignant neoplasms. The first description of
arteriosystemic venous shunting with a cavernous hemangioma
(Fig. 8A,
Fig. 8B,
Fig. 8C,
Fig. 8D,
Fig. 8E) was seen in the
setting of HCC and arterioportal shunting
[8]. Whether the
arteriosystemic shunting was related to the arterioportal shunting was
unclear. The actual incidence of arteriosystemic shunting in the setting of
HCC is unknown, but the incidence of hepatic venous invasion by tumor is
thought to be approximately 15%
[10]. Therefore, when
arteriosystemic shunting to the hepatic veins is observed, invasion of the
hepatic veins by HCC should be suspected
(Fig. 9A,
Fig. 9B).

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Fig. 8. 65-year-old woman with hemangioma and arteriosystemic shunt.
A, Contrast-enhanced arterial phase CT scan shows wedge-shaped
increased attenuation in right lobe of liver with enlarged right hepatic vein
(arrow) and early venous filling representing arteriosystemic venous
shunting.
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Fig. 8. 65-year-old woman with hemangioma and arteriosystemic shunt.
B, Caudal arterial phase CT scan shows vascular subcapsular lesion
with peripheral nodular enhancement consistent with hemangioma
(arrowheads).
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Fig. 8. 65-year-old woman with hemangioma and arteriosystemic shunt.
D, Arterial phase coronal contrast-enhanced three-dimensional
spoiled gradient-recalled MR angiogram shows nodular peripheral enhancement of
subcapsular hemangioma (arrow). Wedge-shaped area of increased
intensity surrounding lesion is also shown (arrowheads).
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Fig. 8. 65-year-old woman with hemangioma and arteriosystemic shunt.
E, Portal venous coronal contrast-enhanced three-dimensional spoiled
gradient-recalled MR angiogram shows filling of subcapsular lesion
(arrow) and wedge-shaped enhancement becoming isointense to healthy
hepatic parenchyma.
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Fig. 9. 45-year-old man with hepatocellular carcinoma and arteriosystemic
shunt.
A, Contrast-enhanced arterial phase CT scan shows hypervascular mass
in right lobe of liver with early filling of dilated right hepatic vein
(arrow), representing arteriosystemic venous shunting.
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