AJR 2000; 174:455-461
© American Roentgen Ray Society
Helical CT
Diagnostic Pitfalls of Arterial Phase Imaging of the Upper Abdomen
Bruce A. Urban1,
Patricia A. McGhie and
Elliot K. Fishman
1
All authors: The Russell H. Morgan Department of Radiology and Radiological
Science, Johns Hopkins Medical Institutions, Baltimore, MD 21287.
Received May 11, 1999;
accepted after revision July 2, 1999.
Address correspondence to B. A. Urban, Department of Radiology, Johns
Hopkins Hospital, 600 N. Wolfe St., Baltimore, MD 21287.
Presented at the annual meeting of the American Roentgen Ray Society, New
Orleans, May 1999.
Introduction
Helical CT is routinely used in evaluation of the abdomen and pelvis.
Advantages of helical CT scanning, including rapid volumetric data acquisition
and optimal contrast enhancement, enable accurate diagnosis of a wide spectrum
of disease processes [1].
However, early arterial phase scanning can result in various phenomena that
are potential diagnostic pitfalls if not appropriately recognized
[2,
3,
4,
5,
6]. Many of these pitfalls
result from early parenchymal enhancement or partial vascular
opacificationespecially in the parenchymal organs of the upper abdomen,
most notably in the liver. In addition, the appearance of true disease during
the arterial phase can at times be misleading or nonspecific. This report
provides an overview of potential pitfalls of arterial phase imaging of the
liver, pancreas, and spleen.
Arterial Phase Helical CT: Indications and Technique
Arterial phase helical CT refers to any acquisition obtained during peak
arterial contrast opacification. Arterial phase CT images are often obtained
when hypervascular tumors or metastases are suspected or when vascular anatomy
is of particular interest, particularly in evaluation of the liver or kidneys
[1]. Acquisitions obtained
during the arterial phase are often combined with images obtained during other
phases of enhancement in the evaluation of most solid abdominal organs
[1]. Arterial phase images of
the upper abdomen produce marked enhancement of the aorta and major arteries,
the spleen, pancreas, and renal cortex.
The specific protocol for obtaining arterial phase helical CT images varies
depending on the clinical indication and the region of interest
[1]. Typically, arterial phase
images are obtained 20-30 sec after the onset of peripheral IV injection of
120-150 ml of iodinated contrast material. The optimal rate of injection is
usually 3-4 ml/sec. The degree of enhancement is dependant on the rate and
timing of the injection and the patient's cardiac output and body habitus.
Thin-collimation (2- to 3-mm) images are ideal for evaluation of vascular
anatomy; a slightly thicker collimation (5 mm) is used for evaluation of most
solid organs. Depending on the organ of interest and the clinical indication,
arterial phase scans are often supplemented with additional helical
acquisitions (dual-phase helical CT).
Liver
Arterial phase imaging is particularly important for evaluation of the
liver [1]. Some lesions are
markedly vascular and are best seen on the arterial phase acquisition. In
addition, arterial phase imaging is used for evaluation of the anatomy of the
hepatic artery. Arterial phase images are usually obtained in conjunction with
a portal venous phase acquisition, typically obtained 70-90 sec after IV
injection of contrast material.
Arterial phase imaging can reveal a variety of pseudolesions, most of which
result from normal vascular variations or changes in the normal dual blood
supply to a portion of liver
[2,
3,
4]. Common pseudolesions are
seen in the gallbladder fossa, the porta hepatis, and the medial segment of
the left lobe of the liver near the falciform ligament
[4]
(Fig. 1). A transient hepatic
attenuation difference of increased enhancement can mimic true disease but is
often the result of vascular compromise or thrombosis
[4]. Hyperattenuation in the
region of thrombosis results from compensatory increased hepatic arterial flow
and the lack of dilution of contrast material during the arterial phase
because of the diminished, nonopacified early portal venous return. Transient
attenuation differences from peripheral portal vein occlusion have a
wedge-shaped distribution [4]
(Fig. 2A,
2B). Complete portal vein
thrombosis can result in diffuse peripheral hyperenhancement if central
cavernous transformation has developed
(Fig. 3). Extrahepatic vascular
causes, notably occlusion of the superior vena cava, can produce a striking
hyperenhancement of the medial segment of the left lobe via collateral
inferior epigastric pathways (Fig.
4).

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Fig. 1. 76-year-old woman with hepatic pseudolesion near falciform ligament.
Arterial phase helical CT scan shows characteristic flow-related pseudolesion
(arrow) in medial segment of left lobe of liver. This pseudolesion is
the most common one seen during arterial phase and is related to separate
venous drainage into left gastric veins. It is often mistaken for tumor;
characteristic appearance and anatomic localization are keys to accurate
diagnosis. Focal fat can have similar appearance.
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Fig. 2A. 52-year-old woman with transient hepatic attenuation difference from
peripheral portal vein thrombosis. Arterial phase helical CT scan reveals
peripheral hypervascular transient hepatic attenuation difference
(arrowheads). Hyperattenuation in liver distal to thrombosis results
from combination of compensatory hepatic arterial flow and diminished early
portal venous return.
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Fig. 2B. 52-year-old woman with transient hepatic attenuation difference from
peripheral portal vein thrombosis. Portal venous phase helical CT scan shows
homogeneously enhanced liver. Small peripheral portal vein thrombus is now
appreciated (arrow).
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Fig. 3. 44-year-old man with hepatic pseudolesions from portal vein
thrombosis. Arterial phase helical CT scan reveals circumferential
hyperperfusion (arrowheads) in patient with complete portal vein
thrombosis (arrow).
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Fig. 4. 27-year-old woman with lymphoma and superior vena cava obstruction.
Arterial phase helical CT scan reveals marked early enhancement in medial
segment of left lobe of liver (arrow). Collaterals from superior vena
cava obstruction involve inferior epigastric veins and course through liver,
resulting in characteristic enhancing pseudolesion. Large lymphoma filled
anterior mediastinum (not shown).
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Other pitfalls of arterial phase imaging include lesion detection and
characterization. Unopacified hepatic veins can be mistaken for true lesions
and decrease lesion conspicuity
[2,
3] (Fig.
5A,
5B). Poor hepatic parenchymal
enhancement markedly limits detection of hypovascular tumors, which are best
seen on portal venous phase images
[5]. Large tumors can be
entirely missed (Fig. 6A,
6B). In the trauma patient,
lack of early enhancement can also make detection of liver lacerations
problematic. Vascular hepatic tumors can often mimic the appearance of
aneurysms or vascular malformations (Figs.
7 and
8). In addition, enhancement
of vascular tumors can be brief and transient, making localization difficult
at biopsy. Peripheral enhancement of hemangiomas can be difficult to
appreciate during the arterial phase (Fig.
9A,
9B). Nodular enhancement of
hemangiomas is more typical.

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Fig. 5A. 31-year-old woman with metastatic colonic cancer. Arterial phase
helical CT scan shows many hypodense lesions, of which only one is true
metastasis. Unfortunately, lesion detection can be difficult and lesion
conspicuity can be markedly compromised during arterial phase imaging.
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Fig. 6A. 54-year-old woman with multiple hepatic adenomas. Arterial phase
helical CT scan reveals subtle inhomogeneous hepatic enhancement. Because most
contrast material reaches liver via portal vein, arterial phase images
typically show poor parenchymal enhancement, which can severely limit lesion
detection as shown in this case.
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Fig. 6B. 54-year-old woman with multiple hepatic adenomas. Portal venous
phase helical CT scan reveals many lesions (arrowheads), which can
now be seen easily because lesions are contrasted against enhanced liver.
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Fig. 7. 41-year-old woman with metastatic islet cell tumor. Arterial phase
helical CT scan reveals homogeneously enhancing hypervascular metastasis in
liver (arrow). Hypervascular tumors can be difficult to differentiate
from vascular lesions and aneurysms.
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Fig. 8. 66-year-old man with hepatic artery pseudoaneurysm. Arterial phase
helical CT scan shows enhancing hepatic artery pseudoaneurysm
(arrow). Note similar appearance of hepatic artery pseudoaneurysm and
enhancing metastatic islet cell tumor shown in
Figure 7.
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Fig. 9A. 72-year-old man with small hemangioma. Arterial phase helical CT
scan shows focal lesion (arrowhead) with subtle peripheral
nodularity. Early phase arterial acquisitions often show hemangiomas before
peripheral enhancement and, as a result, such hemangiomas are often classified
as indeterminate or misdiagnosed as tumors.
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Arterial phase imaging in patients with primary or secondary parenchymal
liver disease can produce problematic enhancement patterns
(Fig. 10). Portal hypertension
can delay hepatic enhancement and underestimate parenchymal disease or produce
portal vein pseudothrombosis (Figs.
11A,
11B and
12A,
12B,
12C,
12D). Peripheral arterioportal
venous shunts are sometimes seen on arterial phase images and can mimic small
tumors [6]
(Fig. 13).

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Fig. 10. 40-year-old woman with hepatic congestion after heart
transplantation. Arterial phase helical CT scan shows markedly inhomogeneous
hepatic enhancement. Heart failure and hepatic congestion can produce mosaic
pattern of hepatic enhancement. Arterial phase scanning can markedly
exaggerate this appearance, which should not be mistaken for infiltrative
tumor. Mild ascites is present.
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Fig. 11B. 47-year-old woman with autoimmune hepatitis, cirrhosis, and hepatic
necrosis. Portal venous helical CT scan better reveals more extensive
heterogeneous hepatic enhancement from necrosis, which was proven at biopsy.
Evaluation of arterial phase images alone can lead to underestimation of liver
disease because images are obtained before peak parenchymal enhancement. This
limitation can be especially problematic in imaging of the cirrhotic
liver.
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Fig. 12A. 41-year-old woman with cirrhosis and pseudothrombosis of portal vein
and superior mesenteric vein. Arterial phase helical CT scan of liver shows
apparent portal vein thrombosis (arrow). Pseudothrombosis is most
commonly encountered in patients with portal hypertension and delayed portal
venous return. Note hepatic cirrhosis and ascites.
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Fig. 12B. 41-year-old woman with cirrhosis and pseudothrombosis of portal vein
and superior mesenteric vein. Arterial phase helical CT scan near pancreas
shows apparent superior mesenteric vein thrombosis (arrow).
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Fig. 12D. 41-year-old woman with cirrhosis and pseudothrombosis of portal vein
and superior mesenteric vein. Portal venous phase helical CT scan reveals
patent superior mesenteric vein (arrow) with no evidence of mass.
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Fig. 13. 47-year-old man with cirrhosis and peripheral hypervascular lesions.
Arterial phase helical CT scan reveals several small hypervascular lesions
(arrows). Detection and characterization of very small lesions using
arterial phase CT scans is difficult. Many of these lesions may be considered
indeterminate and may simply represent small arterioportal venous shunts.
Workup and follow-up appropriate for these small lesions remain ambiguous.
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Pancreas
Arterial phase helical CT is useful in staging pancreatic cancer and in
detecting hypervascular pancreatic tumors, particularly islet cell tumors. A
pitfall of arterial phase imaging can result when a portal vein confluence is
unopacified, thus simulating the appearance of a thrombus or tumor (Fig.
12A,
12B,
12C,
12D). Venous encasement by
tumor can be underestimated [7]
(Fig. 14A,
14B). In addition, enhancement
of the normal pancreas and peripancreatic vasculature can be pronounced,
making hypovascular solid tumors mistakenly appear cystic (Fig.
15A,
15B).

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Fig. 14A. 59-year-old man with unresectable pancreatic tumor. Arterial phase
helical CT scan shows unopacified portal vein and superior mesenteric vein,
thus visualization of vascular encasement is markedly limited.
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Fig. 14B. 59-year-old man with unresectable pancreatic tumor. Portal venous
phase helical CT scan produces adequate venous opacification and reveals
superior mesenteric vein occlusion (arrow).
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Fig. 15A. 40-year-old woman with pancreatic tumor mimicking pseudocyst.
Arterial phase helical CT scan shows lesion that was initially diagnosed as
pseudocyst (arrow). In fact, lesion represents low-density solid
adenocarcinoma. As shown in this case, arterial phase helical CT can produce
contrast enhancement of normal vessels and parenchyma that is so marked that
hypovascular solid masses appear cystic. Similar difficulties can occur when
evaluating renal masses. Note tiny hepatic metastases are present
(arrowheads).
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Fig. 15B. 40-year-old woman with pancreatic tumor mimicking pseudocyst.
Arterial phase helical CT scan obtained at 3-month follow-up reveals marked
increase in size of liver metastases (arrowheads). To avoid this
potential pitfall, obtain density values when evaluating any potentially
cystic mass.
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Spleen
Variable contrast enhancement of the normal spleen during arterial phase
imaging results from differential flow through the vascular sinusoids of the
red pulp [2,
3,
8]. Patterns of normal
inhomogeneous enhancement are typically sinusoidal or cordlike and can be
easily differentiated from true splenic disease in most patients
(Fig. 16). Rarely, the
appearance of the normal spleen during the arterial phase can mimic disease.
Obtaining delayed images may be helpful in confusing cases.

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Fig. 16. 50-year-old man with splenic pseudolesions. Arterial phase helical
CT scan reveals normal inhomogeneous enhancement of spleen. Typically, this
finding is only seen on arterial phase acquisition and is exaggerated in
patients with heart failure, splenic vein occlusion, or portal hypertension.
Inhomogeneous enhancement results from variable flow rates through red pulp
and should not be confused with splenic lacerations.
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Conclusion
Familiarity with the common pitfalls of arterial phase imaging is essential
for accurate detection and characterization of disease in the liver, pancreas,
and spleen. Correlation with an additional portal venous acquisition
(dual-phase helical CT) is often necessary, especially in the evaluation of
hepatic disease.
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