DOI:10.2214/AJR.05.0847
AJR 2006; 187:676-681
© American Roentgen Ray Society
Prevalence and Types of Main and Right Portal Vein Branching Variations on MDCT
Çetin Atasoy1 and
Elif Özyürek1
1 Both authors: Department of Radiology, Ankara University Medical School, Ibn-i
Sina Hospital, Sihhiye 06100, Ankara, Turkey.
Received May 19, 2005;
accepted after revision August 8, 2005.
Address correspondence to Ç. Atasoy
(atasoy{at}medicine.ankara.edu.tr).
Abstract
OBJECTIVE. Our objective was to investigate the prevalence of
variant main and right portal vein ramification in a large group of
patients.
SUBJECTS AND METHODS. The study group consisted of 200 patients who
underwent consecutive contrast-enhanced abdominal CT examinations performed
with an 8-MDCT scanner. Two observers evaluated both thin axial sections and
3D maximum-intensity-projection and volume-rendered images for branching
patterns of the main and right portal veins.
RESULTS. Conventional main portal vein anatomy was present in 64.5%
of the patients. In 9.5% of the patients, the main portal vein trifurcated
into the left portal and right anterior and posterior portal veins. In 23.5%
of the patients, the main portal vein divided into a common left portal
vein-right anterior portal vein trunk and the right posterior portal vein.
Three patients (1.5%) had miscellaneous variations. Twenty-two (16.8%) of 131
patients with conventional main portal vein branching had variant right portal
vein branching, most of which was a trifurcation, followed by an abnormally
proximal origin of the segment VII vein from the right portal vein.
CONCLUSION. Variant main portal vein branching seems to be very
frequent. Common right anterior portal vein-left portal vein trunk is far more
common than trifurcation. Although less frequent, variations also occur in
right portal vein branching.
Keywords: CT angiography liver MDCT
Introduction
Branching anomalies of the main portal vein (MPV) at the hepatic hilum are
known to be less frequent than those of the hepatic arteries, hepatic veins,
and biliary ducts
[1-4].
Although many of these variations can be managed safely with new surgical
techniques [3,
5,
6], some continue to be
contraindications to living donor right lobectomy or they at least make
surgery difficult. The most suitable portal vein anatomy for right lobe living
donor liver transplantation is the presence of conventional MPV branching, in
which the right anterior portal vein (RAPV) and right posterior portal vein
(RPPV) originate from the right portal vein (RPV). In this situation, only one
portal vein anastomosis is made between the recipient's MPV and donor's RPV.
When the RAPV and RPPV originate directly from the MPV or when the RAPV arises
from the left portal vein (LPV), two portal vein anastomoses are needed,
increasing the risk of postoperative portal vein thrombosis
[4]. If these duplicated portal
branches are close to each other, reconstruction with the bifurcation of the
recipient's portal vein can be performed easily. When, however, the RAPV
branches from the LPV more distally or within the parenchyma, an interposed
vein graft is needed for reconstruction, making transplantation a challenging
and high-risk task [3]. The
reported incidence of portal vein variations ranges from 0.09% to 24%
[7-10].
This discrepancy may be due to the use of different sample sizes and
variations in the techniques used to outline the portal anatomy. The relative
frequency of a particular anomaly differs in various studies, the most
frequent anomaly being a trifurcated MPV
[4,
8,
11-15].
This study was conducted to determine the incidence and types of variant
portal anatomy in a large series of patients undergoing abdominal MDCT.
Subjects and Methods
Two hundred patients undergoing abdominal MDCT examinations comprised the
study group. Patients were selected consecutively. Excluded were patients with
large hepatic masses that might have distorted the intrahepatic portal venous
anatomy and those whose images were of poor quality, mainly because of
insufficient portal venous opacification and motion artifacts. Indications for
the examinations were known or suspected malignant disease in 149 cases,
suspected intraabdominal abscess in 13 cases, abdominal pain in 12 cases,
biliary obstruction in seven cases, hepatic mass in six cases, intestinal
obstruction in five cases, trauma in five cases, acute pancreatitis in two
cases, and follow-up of abdominal aortic aneurysm in one case. One hundred
three (51.5%) of the patients were men and boys, and 97 (48.5%) were women and
girls. The age range was 9-83 years (mean age, 49.9 years).
All examinations were performed with an 8-MDCT scanner (LightSpeed Ultra,
GE Healthcare). Scan parameters were 8 x 2.5 mm collimation, 35 mm/s
table feed, 2.5 mm section thickness, 1.25 mm reconstruction interval, 120 kV,
350 mA, and 0.5 seconds rotation time. Portal venous phase images for
evaluation of the portal venous anatomy were obtained with a scan delay of 70
seconds after IV injection of 100 mL of nonionic 350 mg I/mL contrast medium
(iohexol, Omnipaque 350, GE Healthcare) at an injection rate of 3 mL/s. Axial
images were transferred to a workstation (Advantage Windows 4.0, GE
Healthcare), where analyses of the portal venous anatomy were done by two
independent reviewers experienced in the evaluation of the hepatic vascular
anatomy and in 3D image rendering. After axial images were assessed, 3D
reconstructions of the relevant anatomy were performed with the maximum
intensity projection and volume-rendering methods.
Conventional portal anatomy, which was categorized as type 1, was accepted
as the MPV bifurcating into the RPV and LPV, the RPV then dividing into the
RAPV and RPPV. Any deviation from this pattern was regarded as variant
anatomy. Trifurcation of the MPV into the LPV, RAPV, and RPPV was categorized
as type 2, and separate origin of the RPPV from the MPV with emergence of the
LPV and RAPV from a common trunk was accepted as type 3.
Table 1 shows the categories of
MPV branching. As suggested by Hwang et al.
[16], differentiation between
type 2 and type 3 was made according to the shape of the gap between the RAPV
and the RPPV. If the gap was triangular, the anatomy was classified as type 2;
if the gap was rectangular, as type 3. In patients with type 3 anatomy, the
length of the common RAPV-LPV trunk was measured from its origin to its
bifurcation. Other, miscellaneous portal vein variations, in particular
dominant or codominant portal supply of the left lobe arising from the right
lobe veins, also were noted. We looked for portal vein branches traversing the
anatomic border between the right and left lobes of the liver, that is, the
middle hepatic vein and Cantlie's line drawn between the inferior vena cava
and the gallbladder fossa. When we found a branch, we measured its diameter on
axial images. We also searched for any deviations of RPV branching from the
conventional pattern, which includes division into the RAPV and RPPV, further
giving off branches that supply segments V and VIII and segments VI and VII,
respectively. After independent evaluations, findings were compared, and any
discrepancies were resolved with a third consensus reading.

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Fig. 1 34-year-old man with type 1 main portal vein (MPV) anatomy.
Maximum-intensity-projection image, oblique coronal view, shows MPV
bifurcating into left portal vein (LPV) and right portal vein (RPV), which
later divides into right anterior portal vein (RAPV) and right posterior
portal vein (RPPV).
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Because we studied the portal venous anatomy of patients undergoing routine
abdominal MDCT for various clinical reasons, approval by the institutional
ethical committee was not required.
Results
Table 2 shows the relative
frequencies of each type of MPV branching. Of the total of 200 patients, 131
(65.5%) had conventional portal venous anatomy (type 1)
(Fig. 1). Nineteen (9.5%) of
the patients had trifurcation (type 2) (Figs.
2A and
2B), and 47 (23.5%) had type 3
anatomy, whereby the RAPV and the LPV shared a common trunk (Figs.
3A,
3B, and
3C). In patients with type 3
anatomy, the length of the common RAPV-LPV trunk ranged from 2.5 to 17.3 mm
(mean, 7.9 mm). There were miscellaneous variations in three patients: One had
an LPV arising from the RAPV. In one patient the LPV was absent, and the RAPV
had branches that supplied the left lobe. In the third patient the left lobe
had a codominant portal supply, one vein from the LPV and the other from the
RAPV. These two veins anastomosed in the intersegmental fissure. In each of
these three patients either dominant or codominant veins of the left lobe
crossed the interlobar boundary. We did not see dominant venous supply of the
left lobe arising from the right veins or dominant venous supply of the right
lobe originating from the LPV in other patients. There were, however, tiny
portal branches traversing the border between the right and left lobes in 13
(6.5%) of the patients. The diameter of these vessels ranged from 0.5 to 2.7
mm (mean, 1.53 mm) (Table 3).
Nine veins originated from the LPV and supplied segment VIII; four veins
originated from the right side and supplied segment IV.

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Fig. 2A 58-year-old man with type 2 main portal vein (MPV) anatomy.
Volume-rendered image, left superior view, shows MPV dividing into left portal
vein (LPV), right anterior portal vein (RAPV), and right posterior portal vein
(RPPV).
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Fig. 3A 45-year-old woman with type 3 main portal vein (MPV) anatomy.
Volume-rendered image, anteroinferior view, shows MPV bifurcating into right
posterior portal vein (RPPV) and common trunk (RAPV-LPV) that gives rise to
left portal vein (LPV) and right anterior portal vein (RAPV).
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One hundred nine (83.2%) of 131 patients with conventional MPV branching
also had conventional RPV branching (Fig.
4), whereas 22 (16.8%) of these patients had variant RPV
branching. Sixteen (12.2%) of the patients had RPV trifurcation. In seven of
these patients the RPV trifurcated into the RAPV and segment VI and segment
VII veins (Fig. 5); in two
patients, into the RAPV and RPPV and a common trunk that supplied branches to
segments V and VI; in two patients, into the RAPV and RPPV and a separate
segment V vein; in two patients, into the RAPV and RPPV and a separate segment
VI vein; and in one patient, into the RAPV and RPPV and a separate segment
VIII vein. One (0.8%) of the patients had RPV quadrifurcation into the RAPV,
segment V vein, segment VI vein, and segment VII vein. In five (3.8%) of the
patients, a segment VII vein originated proximal to the division of the RPV,
which later bifurcated into the RAPV and segment VI vein in four patients
(Figs. 6A,
6B, and
6C) and into the RAPV and a
common vein that supplied branches to segments V and VI in one patient.
Table 4 shows the relative
frequencies of RPV branching patterns in patients with type 1 MPV
branching.

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Fig. 4 49-year-old man with conventional right portal vein (RPV)
branching. Volume-rendered image, posterosuperior view, shows RPV bifurcating
into right anterior portal vein (RAPV) and right posterior portal vein (RPPV).
MPV = main portal vein, LPV = left portal vein.
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Fig. 5 16-year-old girl with trifurcation of right portal vein
(RPV). Volume-rendered image, superior view, shows RPV trifurcating into right
anterior portal vein (RAPV), segment VII vein (SVII vein), and segment VI vein
(SVI vein). MPV = main portal vein, LPV = left portal vein.
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Fig. 6A 70-year-old woman with abnormally proximal origin of segment
VII vein (SVII vein). Volume-rendered image, superior view, shows SVII vein
originating from right portal vein (RPV) proximal to its bifurcation into
right anterior portal vein (RAPV) and segment VI vein. MPV = main portal vein,
LPV = left portal vein, RAPV = right anterior portal vein, SVI vein = segment
VI vein.
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Fig. 6B 70-year-old woman with abnormally proximal origin of segment
VII vein (SVII vein). Axial images show abnormally proximal origin of SVII
vein from RPV. B shows distal part of SVII vein supplying
posterosuperior part of right lobe. C shows origin of SVII vein from
right portal vein.
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Fig. 6C 70-year-old woman with abnormally proximal origin of segment
VII vein (SVII vein). Axial images show abnormally proximal origin of SVII
vein from RPV. B shows distal part of SVII vein supplying
posterosuperior part of right lobe. C shows origin of SVII vein from
right portal vein.
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TABLE 4: Relative Frequencies of Right Portal Vein Branching Patterns in Patients
with Type 1 Main Portal Vein Branching
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The findings of both observers were in very high agreement for
classification of the MPV and RPV branching patterns. Discordant
classifications were resolved by consensus in five cases. In one of these
cases type 1 MPV anatomy was classified as type 2 anatomy by one of the
reviewers. In the remaining 199 (99.5%) of the patients MPV anatomy was
classified in the same manner by both observers. There was, however, slightly
higher discordance regarding classification of the RPV branching pattern.
Findings were discrepant in four of 131 patients with type 1 MPV anatomy in
whom an RPV existed. All these patients had trifurcated RPVs that were
classified as conventional RPV branching by one reviewer. RPV branching
classifications were in agreement for 127 (97%) of the patients.
Discussion
Presurgical awareness of variant portal venous anatomy is important before
graft procurement in liver transplantation, hepatic tumor resection, and
placement of transjugular intrahepatic portosystemic shunts and for accurate
tumor localization. Previous studies have shown the prevalence of variant
portal venous anatomy ranges from 0.09% to 24%
[7-10].
The prevalence in our series (34.5%) was considerably higher. We believe our
figure reflects the true prevalence, because our series of patients was
relatively large, and we meticulously evaluated both thin axial sections and
reformatted 3D images. Studies in which only thick axial CT slices were
assessed revealed prevalences between 6% and 13.8%
[8,
12,
13]. It is possible that many
variations have been missed on these thick axial images. Several studies in
which MDCT was used showed more frequent portal vein variations, ranging from
20% to 24% [4,
9,
17]. Although the technique in
those studies was similar to the one we used, the prevalence of variations was
still considerably lower than our findings, possibly because of their
relatively small sample sizes. In a large angiography study, Cheng et al.
[18] found portal vein
variations in 30% of patients, a figure similar to ours.
The relative frequencies of various portal vein branching types in our
study also were different than in previous studies. Unlike the majority of
previous studies, in which trifurcation was the most frequent variation
[4,
8,
11-15],
our study showed a common RAPV-LPV trunk was almost 2.5 times more common than
trifurcation. This striking difference may have been the result of use of
different methods of imaging the portal venous ramification. We believe that
on thick axial sections a short RAPV-LPV trunk, which was not infrequent in
our experience, can easily be misclassified as trifurcation. Reformations in
3D are crucial for accurate visualization of the anatomy in such cases. To
differentiate a short RAPV-LPV trunk from trifurcation, we used the criteria
described by Hwang et al.
[16], who classified the
anatomy as type 3 (i.e., common RAPV-LPV trunk) in instances in which the gap
between the RAPV and the RPPV was rectangular.
Differentiation of type 3 from type 2 anatomy has several advantages: In
most donors with type 2 anatomy, despite the absence of an RPV, a single
portal lumen can be obtained from the RAPV and RPPV owing to their close
approximation. Type 3 anatomy, however, makes surgery more complicated,
because two transections of the RAPV and RPPV are needed, resulting in two
portal lumens in the right lobe graft
[1]. The length of the common
RAPV-LPV trunk has important surgical implications. When they are close to
each other, two donor portal branches can be anastomosed to the recipient's
portal bifurcation; that is, the donor RPPV is anastomosed to the recipient's
RPV, and the donor RAPV is anastomosed to the recipient's LPV. Such Y-grafts
allow simultaneous reperfusion through both donor portal branches. When the
donor veins are widely spaced, however, as with a long RAPV-LPV trunk, an
extension-type graft may be needed for reconstruction of the donor RAPV. This
step can result in delayed reperfusion of a segment of the graft
[6]. The average length of the
RAPV-LPV trunk in our series was 7.9 mm. As far as we know, no cut-off value
has been reported for length of the RAPV-LPV trunk above which surgeons have
to use an extension graft. Unlike in right lobe transplantation, in right
posterior segment procurement the presence of type 3 anatomy is more desirable
in donor selection. Hwang et al.
[16] reported that almost no
candidate with type 1 and only 3.6% of those with type 2 anatomy were suitable
for right posterior graft procurement, whereas 35.2% of patients with type 3
portal veins had suitable anatomic features for this procedure.
Dominant portal venous supply of segment IV arising from the RPV may
contraindicate right lobectomy in liver transplantation candidates. This rare
situation was found in 2% of the population in one study
[14]. Other studies have shown
widely varying frequencies from 0%
[1,
4,
9,
17] to 32.5%
[5]. We found major portal
veins crossing the interlobar boundary to supply segment IV in 1.5% of
patients, although surgically insignificant small veins that originated from
the RPV and supplied segment IV were present in another 2% of the study
group.
We found no patients with dominant portal venous supply of the right liver
segments originating from the LPV, which is a relative contraindication to
right lobe harvesting [14].
Nevertheless, nine (4.5%) of the patients had small veins originating from the
left portal system and supplying the right lobe. The largest of these veins
was 2.7 mm in diameter. Such tiny veins do not hinder liver donation or tumor
resection and are ligated during surgery.
To our knowledge, variations in RPV ramification have not been described in
the radiology literature. These variations are not rare, having been found in
33.5% of cases in a cadaveric dissection study
[19]. We found variant RPV
ramification in 22 (16.8%) of 131 patients with type 1 MPV branching. There
were several types of variations, but the most common was trifurcation, which
most frequently involved separate origins of segment VI and VII veins from the
RPV, as was also the case in the study by Hata et al.
[19]. In five patients the
segment VII vein arose from the RPV proximal to its bifurcation. In three
patients segment V and segment VI veins ramified from a common trunk. The
latter variation can hinder identification of the anterior border of segment
VI [19]. Preoperative
awareness of variant RPV branching may be beneficial in right posterior
segment harvesting and in segmental resection involving the right lobe.
Lack of pathologic confirmation of the findings may be considered a
limitation of our study. However, our purpose was not to show the accuracy of
CT in the detection of various portal vein variations. Rather we aimed to
learn the prevalence of variant portal venous anatomy in a large population by
using MDCT, which has been reliably used to map portal veins in persons who
are candidates for live liver donation.
In conclusion, variant ramification of the MPV may be more common than
previously reported. Unlike previous studies, our study showed that the
frequency of type 3 anatomy (i.e., a common RAPV-LPV trunk) far exceeds that
of trifurcation. The RPV also seems to have a considerable rate of variant
branching with several different patterns, some of which may influence
decision making regarding right lobe surgery.
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A. M. Covey and K. T. Brown
Prevalence of Right Portal Vein Branching Anomalies
Am. J. Roentgenol.,
May 1, 2007;
188(5):
W492 - W492.
[Full Text]
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C. Atasoy and E. Ozyurek
Reply
Am. J. Roentgenol.,
May 1, 2007;
188(5):
W493 - W493.
[Full Text]
[PDF]
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