AJR F and L Medical Products: Radiation Protection & More
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Asayama, Y.
Right arrow Articles by Honda, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Asayama, Y.
Right arrow Articles by Honda, H.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Hotlight (NEW!)
Right arrow
What's Hotlight?
DOI:10.2214/AJR.04.1417
AJR 2006; 186:440-448
© American Roentgen Ray Society


Original Research

MDCT of the Gonadal Veins in Females with Large Pelvic Masses: Value in Differentiating Ovarian Versus Uterine Origin

Yoshiki Asayama1, Kengo Yoshimitsu1, Hitoshi Aibe1, Akihiro Nishie1, Daisuke Kakihira1, Hiroyuki Irie1, Tsuyoshi Tajima1, Kunishige Matake1, Tomohiro Nakayama1, Yoshihiro Ohishi2, Eisuke Kaneki2 and Hiroshi Honda1

1 Department of Clinical Radiology, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
2 Department of Anatomic Pathology, Kyushu University, Fukuoka 812-8582, Japan.

Received September 12, 2004; accepted after revision January 28, 2005.

 
Address correspondence to Y. Asayama (asayama{at}radiol.med.kyushu-u.ac.jp).


Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The objective of our study was to determine the usefulness of recognizing the continuity of the gonadal veins to the pelvic mass to differentiate ovarian versus uterine origin on MDCT in females with a large pelvic mass.

MATERIALS AND METHODS. Two radiologists interpreted the MDCT images obtained on a monitor, using paging methods, in 86 female patients with a large pelvic mass (> 8 cm) and 40 patients without an abdominopelvic mass as control subjects. The following issues were recorded using a 5-point scale: visualization of gonadal veins and origin determination based on anatomic continuity. Receiver operating characteristic (ROC) curve analysis was performed, and the interobserver differences were checked with kappa statistics. The maximum diameters of the gonadal veins were also measured. With consensus interpretations, the sensitivity, specificity, and accuracy of ovarian origin determination were calculated.

RESULTS. Gonadal veins were shown in more than 70% of the subjects in both the control group and the patients with a mass (hereafter referred to as the "mass group"). There was no significant difference in the diameter of the gonadal veins between the control and mass groups and between patients with an ovarian mass and those with a uterine mass. The values for the area under the ROC curve (Az) of the two observers for ovarian origin determination were 0.90 and 0.92. The kappa value was 0.48. The sensitivity, specificity, and accuracy were 83.3%, 87.5%, and 84.9%, respectively.

CONCLUSION. Gonadal veins can be shown on MDCT with high consistency; MDCT provides useful information for determining the origin of relatively large pelvic tumors arising in females.

Keywords: CT • genitourinary tract imaging • gonadal veins • pelvic imaging • pelvic mass • women's imaging


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
To help narrow the differential diagnosis of a pelvic mass in females, it is important to determine the site of origin. Some researchers [1-5] have proposed that the analysis of MRI or sonographic features of the tumor—including its content, architecture, pattern of degeneration, and the relationship of the uterine serosa to the mass—allows differentiation of an ovarian mass from a uterine mass. In routine practice, however, it may not always be possible to determine the site of the origin of a large pelvic tumor [6].

On the other hand, the relationship of a pelvic mass and the gonadal veins on CT when determining the origin of masses has drawn little attention. The purpose of this study, therefore, was to describe the detectability of gonadal veins on routine CT examination and the utility of detecting anatomic continuity of the gonadal veins to pelvic masses to define the organ of origin of pelvic masses, especially masses with an ovarian origin versus those with a uterine origin.


Materials and Methods
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Patient Population
There were 130 consecutive patients who had a large pelvic mass (> 8 cm) that was surgically resected. Of these 130 patients, 86 underwent preoperative MDCT of the abdomen and pelvis with a consistent protocol: 54 had an ovarian tumor (47 epithelial tumors, two metastases, and five others) and 32 had a uterine tumor (28 leiomyomas, one leiomyosarcoma, and three others). These cases were ultimately selected for this study. The patients ranged in age from 19 to 81 years (mean, 52.0 years), and tumor size ranged from 8 to 26 cm (mean, 10.5 cm). An additional 40 females who underwent MDCT during the same period and were found to be free of disease in the abdomen and pelvis were selected as control subjects. They ranged in age from 16 to 81 years (mean, 47.9 years), which is almost exactly equivalent to the age range of the 86 patients with a pelvic mass (p =0.33, Student's t test). Our institutional review board did not require its approval or informed consent for retrospective evaluation of the patients' records and images.

CT Protocol
All patients were examined with a 4-MDCT scanner (Aquilion, Toshiba; or Somatom Volume Zoom, Siemens Medical Solutions). The parameters for scanning were a 2.5- or 3-mm collimation, 5-mm reconstruction, and 5.5 pitch. Scanning from the top of the liver to the pubis was begun 60 and 240 sec after IV injection of 100 mL of a contrast medium containing 300 mg I /mL; the injection rate was 2 mL/sec.

Image Interpretation
Two abdominal radiologists with 10 and 16 years of experience with CT of the abdomen, respectively, were blinded to the surgical results and MRI or sonographic findings; they interpreted independently the axial CT images on a monitor (Coronis 3MP, Barco) using paging methods (the scroll function on a PACS workstation). Visualization of the gonadal veins was scored using the following 5-point scale in both the patients with a mass (hereafter referred to as the "mass group") and the control subjects: 1, not detected; 2, about a quarter detectable; 3, about half the length detectable; 4, about three quarters detectable; and 5, totally detectable. The gonadal veins were tracked backward from the draining point at the inferior vena cava (IVC) or left renal veins in a caudal direction to the pelvis.

The maximum diameters of the gonadal veins were measured on the console by the two observers at the time of interpretation. We measured the gonadal veins in the image at the point where they looked the biggest. Actually, we measured two or three points when the biggest point was uncertain, and the averaged values were compared among the three age groups (≤ 30, 31-59, ≥ 60 years), between patients with and without a pelvic mass, between patients with a mass of ovarian origin and those with a mass of uterine origin, between patients with an ovarian mass and those without a pelvic mass, and between patients with a uterine mass and those without pelvic mass. We also compared the diameters of the gonadal vein between the right and left side in the mass group and control group, respectively, and the mass side and contralateral side in the patients with an ovarian mass.

The origin of the tumors was determined as follows. The mass was considered to be ovarian in origin when the gonadal vein was observed to be continuous to the mass. When the gonadal vein continued to the ovaries, the mass was considered uterine in origin. The diagnostic confidence in determining the origin of the mass, based on the continuity of the gonadal vein and the pelvic mass, was also scored using a 5-point ordinal scale. In this scale, 1 meant the origin was definitely uterine; 2, probably uterine; 3, uncertain; 4, probably ovarian; and 5, definitely ovarian. When the observer rated the mass 4 or 5, the laterality of the gonadal vein that the observer focused on (in other words, the laterality of the mass) was also recorded.

Data Analysis and Statistics
For detection of the gonadal veins, the interobserver difference was evaluated with kappa statistics, and the detectability was then calculated by defining confidence level ratings of 4 and 5 as positive and 3 or less as negative after resolving discrepancies between the two observers by consensus. The degree of interobserver agreement was characterized as slight (0-0.20), fair (0.21-0.40), moderate (0.41-0.60), substantial (0.61-0.80), or almost perfect (0.81-1.00). The chi-square test was used for a comparison of gonadal vein detection between the control group and the mass group; visualization of the gonadal vein in correlation with patient age was tested by Fisher's exact test. For comparison of the diameter of the gonadal vein, the unpaired Student's t test was used. All p values were calculated using statistical software (StatView, Hulinks).

For determination of the origin of each pelvic mass, the receiver operating characteristic (ROC) curve was fitted to each observer, and the area under the ROC curve (Az value) was evaluated for diagnostic accuracy. The computer program ROC-KIT 0.9B (C. E. Metz) was used [7, 8]. Factors with Az values greater than 0.80 were considered to have good diagnostic accuracy [8]. The interobserver difference was evaluated with kappa statistics. The sensitivity, specificity, and accuracy for detecting ovarian origin were calculated by defining confidence level ratings of 4 and 5 as positive and 3 or less as negative; discrepancies between the two observers were resolved by consensus.

When the origin of a mass was misdiagnosed, the reasons for the misdiagnosis were evaluated by the study coordinator. We investigated the reasons of misdiagnosis in cases of ovarian tumors rated 1 or 2 and in cases of uterine tumors rated 4 or 5.


Results
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
The detectability of the gonadal veins in both the control group and mass group was more than 70% with kappa values between 0.41 and 0.52, which shows good correlation. No significant difference was found in detection of gonadal veins on both sides between the control group and the mass group. There was no statistically significant difference in detection of gonadal veins on both sides among the three age groups in either the control or mass group. Details are shown in Tables 1 and 2.


View this table:
[in this window]
[in a new window]

 
TABLE 1: Detectability of Gonadal Veins on MDCT

 

View this table:
[in this window]
[in a new window]

 
TABLE 2: Detection of Gonadal Veins According to Patient Age

 

There was no significant difference between the two observers' measurements of maximum diameter of gonadal veins (p = 0.682, paired Student's t test). The mean diameters of the gonadal veins for the three age groups are shown in Table 3. From the data presented in Table 3, it can be seen that the younger patients had gonadal veins of smaller caliber than did the elderly patients, with statistical significance (p < 0.05). There were no significant differences in the diameter of both gonadal veins between the control group and mass group in each of the three age groups. The diameter of the right gonadal vein in the ovarian mass group (mean ± SD, 4.4 ± 2.1 mm) was significantly smaller than that in the uterine mass group (5.6 ± 4.8 mm) (p = 0.0028). The diameter of the left gonadal vein in the ovarian mass group (4.5 ± 2.3 mm) was smaller than that in the uterine mass group (5.3 ± 2.7 mm), also showing a significant difference (p = 0.039).


View this table:
[in this window]
[in a new window]

 
TABLE 3: Maximum Diameters (mm) of the Bilateral Gonadal Veins According to Patient Age

 

There were no significant differences in gonadal vein diameter between the ovarian mass group and the control group on either side (right: ovarian mass group vs control group, 4.4 ± 2.1 mm vs 4.0 ± 1.7 mm, respectively, p = 0.24; left: ovarian mass group vs control group, 4.5 ± 2.3 mm vs 4.2 ± 2.7 mm, respectively, p = 0.32). There were significant differences in the diameter of the gonadal vein on both sides between the uterine mass group and control group (right: uterine mass group vs control group, 5.6 ± 4.8 mm vs 4.0 ± 1.7 mm, respectively, p = 0.0004; left: uterine mass group vs control group, 5.3 ± 2.7 mm vs 4.2 ± 2.7 mm, respectively, p = 0.0084). There were no significant differences in size between right and left in the control group (right vs left, 4.0 ± 1.7 mm vs 4.3 ± 2.6 mm, p = 0.43) and mass group (right vs left, 4.8 ± 2.5 mm vs 4.8 ± 3.4 mm, p = 0.99). In the ovarian mass group, there was no significant difference in gonadal vein size between the mass side and the contralateral side (mass side vs contralateral side, 4.4 ± 2.2 mm vs 4.0 ± 1.5 mm, respectively; p = 0.28).

For determination of the origin of the pelvic masses, the Az values of the two observers were 0.90 and 0.92, respectively (Fig. 1). The interobserver kappa value was 0.48, showing moderate agreement. For observer 1, sensitivity, specificity, and accuracy were 77.8%, 90.6%, and 82.6%, respectively. For observer 2, sensitivity, specificity, and accuracy were 87.0%, 84.4%, and 86.0%, respectively. Disagreement was resolved by consensus, which was needed for 12 cases (eight right and four left), and sensitivity, specificity, and accuracy values of 83.3%, 87.5%, and 84.9%, respectively, were obtained. In the 45 ovarian tumor cases in which the origin was correctly diagnosed—namely, rated 4 or 5—the laterality of the tumor was also correctly diagnosed in all 45 cases.


Figure 1
View larger version (18K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 1 —Graph shows receiver operating characteristic (ROC) curves of two observers for determination of origin of lesion. Area under ROC curve (Az) values of both observers had good diagnostic accuracy: 0.90 for observer 1 ({diamond}) and 0.92 for observer 2 ({square}), with good interobserver correlation ({kappa} = 0.48).

 
The number of misdiagnoses was 10 and eight for observers 1 and 2, respectively. The major reason for incorrect origin determination was small ovaries, which were considered to obscure the relationship between the gonadal vein and the mass (six and four cases for observers 1 and 2, respectively). Other possible reasons included small gonadal veins (five and four cases for observer 1 and 2, respectively) and little retroperitoneal fat (three and two cases for observers 1 and 2, respectively).


Discussion
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Sonograms and MR images are generally capable of helping determine whether a pelvic mass is uterine or adnexal in origin [1-3, 5, 9]. However, the larger the pelvic mass, the more difficult it is to determine tumor location. The characteristics of the tumor, such as its content, architecture, and pattern of degeneration, are not always helpful in determining the origin of a large pelvic mass [6, 10-14].

Kim et al. [15] reported that the "bridging vascular" sign on MR images—which they described as curvilinear, tortuous vascular signal-void structures crossing, between, or crossing and between the uterus and the mass—was a useful finding for differentiating exophytic subserosal uterine myomas from extrauterine tumors. Mittl et al. [16] also reported that a high-signal-intensity rim surrounding uterine myomas on T2-weighted MR images was a useful sign.

Recently, the use of a high-resolution CT scanner combined with IV contrast medium injection and thinner sections has substantially improved imaging of the female genital tract anatomy and facilitated precise identification of the vascular structures [17]. To our knowledge, however, only one report has been published about a sign on CT that contributes to determining the origin of pelvic masses [18]. The "vascular pedicle" sign, named by Lee et al. [18], is a sign that can be used to indicate ovarian origin of the pelvic mass when the gonadal veins are observed directly joining the mass. That study was performed using a single-detector helical CT scanner, and Lee et al. did not evaluate how often gonadal veins are detectable in patients with or without pelvic masses. We designed the present study to evaluate the detectability of gonadal veins in patients with and in those without a pelvic mass and the diagnostic accuracy of MDCT in determining the origin of pelvic masses using ROC curve analysis.

The normal anatomy of the gonadal vein, as imaged by CT, has been described [17, 19, 20]. The right gonadal vein arises from the right ovarian plexus and lies lateral to the right ureter. It ascends and parallels the right ureter, crossing anteromedially to it approximately halfway between the right gonadal vein-IVC union and the IVC bifurcation. The right gonadal vein then joins the IVC laterally or anterolaterally [19]. The left gonadal vein arises and ascends similarly and drains into the left renal vein instead of the IVC [17].

In healthy patients, we can trace the gonadal veins on MDCT backward from the draining point into the IVC or left renal vein to the adnexal region in approximately 80% of the patients. Although there is no statistically significant difference in the detection of gonadal veins among the three age groups on MDCT, the gonadal veins tended to be less detectable in younger females (≤ 30 years old) than in elderly women (≥ 60 years old) in both the control and mass groups. This was supported by the fact that the diameter of the gonadal veins in the younger population (≤ 30 years old) was significantly smaller than that in the elderly population (≥ 60 years old) when measured on MDCT. This may be related to the parous status of the women. Rozenblit et al. [21] reported that incompetent and dilated ovarian veins were present in 63% of parous women, which was significantly more frequent than the rate in nulliparous women (10%). However, in this study, we did not check the parous status of any of our patients.

The diameter of the gonadal veins in patients with a uterine tumor was significantly larger than that in the patients with an ovarian tumor, whereas there was no significant difference between patients with and without pelvic masses. The diameter of the gonadal vein may be affected by various factors: The gonadal vein conveys venous blood not only from the ovaries, but also from the uterus, and there may even be bidirectional flow, particularly on the left side, where the gonadal vein drains into the left renal vein. Because venous blood volume may be related to the volume of the solid part of the mass, uterine masses (most of which are solid) may drain a larger volume of venous blood than ovarian masses (most of which are cystic), which may explain why the gonadal veins in patients with uterine masses are larger in caliber than in those with ovarian masses [22]. Therefore, we would like to emphasize that what is important in determining the origin of the pelvic mass is the anatomic continuity of the gonadal veins to the pelvic mass, not the diameter or size of the gonadal veins. Another tendency we observed, although it was not statistically significant, was that gonadal veins were less likely to be detected in patients with pelvic masses than in those without. This may be attributable to the fact that the gonadal veins may be compressed by the mass, most typically at the level of the pelvic inlet.

In our study of origin determination, the Az values of the two observers were high (0.90 and 0.92), and the interobserver kappa value of 0.48 showed moderate agreement. The sensitivity, specificity, and accuracy were all approximately 85%, and the organ of origin did not influence whether the observers were correct in consensus or not. We presume that these excellent diagnostic performances were at least partially attributable to the use of an MDCT scanner. MDCT provides substantial improvement in volume coverage and z-axis resolution [23]. In addition, image interpretation with paging methods on the monitor substantially helped the observers trace the gonadal veins in a cephalocaudad direction. On the other hand, despite the high Az value, the intraobserver kappa value showed relatively low agreement. The reason was thought to be that the two observers missed different cases.


Figure 2
View larger version (141K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2A —53-year-old woman with uterine carcinosarcoma. CT image at level of left renal vein.

 


Figure 3
View larger version (139K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2B —53-year-old woman with uterine carcinosarcoma. CT image shows joining point of left gonadal vein (arrow) into left renal vein.

 


Figure 4
View larger version (116K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2C —53-year-old woman with uterine carcinosarcoma. CT image shows right gonadal vein (white arrow) joining to inferior vena cava. Black arrow = left gonadal vein.

 


Figure 5
View larger version (123K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2D —53-year-old woman with uterine carcinosarcoma. CT image of upper level of pelvis shows right (white arrow) and left (black arrow) gonadal veins.

 


Figure 6
View larger version (107K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2E —53-year-old woman with uterine carcinosarcoma. CT images at level of pelvic mass show that gonadal veins continue to bilateral ovarian cystic structures. Bilateral gonadal veins arise from normal ovary (thin black arrows and thin white arrows, F) and are totally detectable to inferior vena cava or left renal vein, respectively. Detectability scores of both bilateral gonadal veins were 5. Score of origin determination was judged by both observers to be 1. Thick white arrows = right gonadal vein, thick black arrows = left gonadal vein.

 


Figure 7
View larger version (103K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2F —53-year-old woman with uterine carcinosarcoma. CT images at level of pelvic mass show that gonadal veins continue to bilateral ovarian cystic structures. Bilateral gonadal veins arise from normal ovary (thin black arrows and thin white arrows, F) and are totally detectable to inferior vena cava or left renal vein, respectively. Detectability scores of both bilateral gonadal veins were 5. Score of origin determination was judged by both observers to be 1. Thick white arrows = right gonadal vein, thick black arrows = left gonadal vein.

 


Figure 8
View larger version (124K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 2G —53-year-old woman with uterine carcinosarcoma. Continuity of gonadal veins and normal ovaries is most easily visualized on curved multiplanar reconstruction, such as this image, which was not shown to either observer. Thick white and black arrows = right and left gonadal veins, thin white and black arrows = normal ovary.

 


Figure 9
View larger version (116K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 3A —59-year-old woman with right ovarian carcinoma. CT image shows large solid mass with central necrosis located in pelvis.

 


Figure 10
View larger version (125K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 3B —59-year-old woman with right ovarian carcinoma. CT images show right gonadal vein (arrow, B and C) arises from solid component of large mass. Score of origin determination was 5—that is, this mass was considered to be right ovarian mass. In addition, stretched venous branches are seen around mass (wraparound phenomenon, arrowheads, C and D). Uterus is not seen in these images.

 


Figure 11
View larger version (121K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 3C —59-year-old woman with right ovarian carcinoma. CT images show right gonadal vein (arrow, B and C) arises from solid component of large mass. Score of origin determination was 5—that is, this mass was considered to be right ovarian mass. In addition, stretched venous branches are seen around mass (wraparound phenomenon, arrowheads, C and D). Uterus is not seen in these images.

 


Figure 12
View larger version (121K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 3D —59-year-old woman with right ovarian carcinoma. CT images show right gonadal vein (arrow, B and C) arises from solid component of large mass. Score of origin determination was 5—that is, this mass was considered to be right ovarian mass. In addition, stretched venous branches are seen around mass (wraparound phenomenon, arrowheads, C and D). Uterus is not seen in these images.

 


Figure 13
View larger version (113K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 4A —49-year-old woman with subserosal pedunculated uterine myoma. CT images show large mass was located adjacent to uterus (U, C). Both gonadal veins (thick black and white arrows) are joined to normal ovarian structures (thin black and white arrows, C). Score of origin determination was 2, of probable nonovarian origin.

 


Figure 14
View larger version (111K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 4B —49-year-old woman with subserosal pedunculated uterine myoma. CT images show large mass was located adjacent to uterus (U, C). Both gonadal veins (thick black and white arrows) are joined to normal ovarian structures (thin black and white arrows, C). Score of origin determination was 2, of probable nonovarian origin.

 


Figure 15
View larger version (118K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 4C —49-year-old woman with subserosal pedunculated uterine myoma. CT images show large mass was located adjacent to uterus (U, C). Both gonadal veins (thick black and white arrows) are joined to normal ovarian structures (thin black and white arrows, C). Score of origin determination was 2, of probable nonovarian origin.

 
According to our observations, in ovarian tumors, gonadal veins frequently coursed along the lateral and dorsal aspect of a large ovarian mass and their branches continued to the surface of the mass, typically in a wraparound fashion (Figs. 2A, 2B, 2C, 2D, 2E, 2F, 2G, 3A, 3B, 3C, and 3D). We thus recognized the stretched gonadal venous branches at the periphery of the mass (in a wraparound fashion) in 38 (70.4%) of 54 cases of ovarian tumors in the current study. The wraparound appearance was seen in only three (9.4%) of the 32 uterine masses. In contrast, in patients with uterine masses, the gonadal veins tended to show abrupt interruption at the lateral edge of the uterine mass, continuing to the normal ovary (Figs. 4A, 4B, 4C, 5A, 5B, and 5C); this was seen in 23 (71.9%) of the 32 uterine masses. This abrupt interruption of the gonadal vein was observed even in three patients with undetectable small ovaries adjacent to the uterine masses. Although these observations were not formally studied in an unblinded fashion, the observation was made during the course of the study. In addition to the information about the continuity of the mass and the gonadal veins, with this sign used as an indicator of uterine origin of the mass, the sensitivity, specificity, and accuracy of the origin determination reached 87.0%, 96.9%, and 93.0%.


Figure 16
View larger version (134K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 5A —45-year-old woman with uterine myoma. CT images show right gonadal vein (arrow) looks as if it continues directly to mass. Both observers diagnosed this lesion as ovarian tumor. Surgery disclosed leiomyoma of uterus. In this case, normal ovary is not visualized, causing misdiagnosis. However, wraparound appearance is not seen, but abrupt interruption of gonadal vein is recognized at lateral edge of mass, which indicates this mass originates from uterus rather than ovary.

 

Figure 17
View larger version (133K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 5B —45-year-old woman with uterine myoma. CT images show right gonadal vein (arrow) looks as if it continues directly to mass. Both observers diagnosed this lesion as ovarian tumor. Surgery disclosed leiomyoma of uterus. In this case, normal ovary is not visualized, causing misdiagnosis. However, wraparound appearance is not seen, but abrupt interruption of gonadal vein is recognized at lateral edge of mass, which indicates this mass originates from uterus rather than ovary.

 

Figure 18
View larger version (129K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 5C —45-year-old woman with uterine myoma. CT images show right gonadal vein (arrow) looks as if it continues directly to mass. Both observers diagnosed this lesion as ovarian tumor. Surgery disclosed leiomyoma of uterus. In this case, normal ovary is not visualized, causing misdiagnosis. However, wraparound appearance is not seen, but abrupt interruption of gonadal vein is recognized at lateral edge of mass, which indicates this mass originates from uterus rather than ovary.

 
There are some limitations of this present study. First, large masses in the female pelvis arise not only from reproductive organs, but also from the gastrointestinal system, urinary system, adjacent soft tissues, peritoneum, or retroperitoneum. Our study did not include cases in which lesions had arisen from nonreproductive organs. In diagnosing those lesions, meticulous evaluation of other venous systems—such as the inferior mesenteric veins for rectosigmoid lesions, the superior mesenteric veins for small intestinal or mesenteric lesions, and the internal iliac veins for retroperitoneal lesions—may be of use in determining the origin of the mass. Additional studies with a larger number of cases that include pelvic masses of both reproductive and nonreproductive origins may clarify this issue.

Second, because this study was retrospective, some patients who had a large pelvic mass did not undergo preoperative CT. This study might not include the patients in whom CT was thought to be unnecessary after a usual sonographic examination. Third, the numbers of patients younger than 30 were small in both the control and mass groups. Fourth, no multivariate analysis was done including age, size of the mass, and so on as possible predictors or to increase accuracy.

In conclusion, gonadal veins were consistently shown on MDCT as observed with paging methods on the console. Differentiation of large pelvic masses with an ovarian origin and those with a uterine origin is possible with an accuracy of approximately 85% by detecting the anatomic continuity of gonadal veins to the masses. This CT sign is a new indicator for determination of the organ of the large pelvic mass.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Dooms GC, Hricak H, Tscholakoff D. Adnexal structures: MR imaging. Radiology 1986;158 : 639-646[Abstract/Free Full Text]
  2. Mitchell DG, Mintz MC, Spritzer CE, et al. Adnexal masses: MR imaging observations at 1.5 T, with US and CT correlation. Radiology 1987;162 : 319-324[Abstract/Free Full Text]
  3. Weinreb JC, Barkoff ND, Megibow A, Demopoulos R. The value of MR imaging in distinguishing leiomyomas from other solid pelvic masses when sonography is indeterminate. AJR 1990;154 : 295-299[Abstract/Free Full Text]
  4. Fried AM, Kenney CM 3rd, Stigers KB, Kacki MH, Buckley SL. Benign pelvic masses: sonographic spectrum. RadioGraphics1996; 16:321 -334[Abstract]
  5. Olson MC, Posniak HV, Tempany CM, Dudiak CM. MR imaging of the female pelvic region. RadioGraphics 1992;12 : 445-465[Abstract]
  6. Szklaruk J, Tamm EP, Choi H, Varavithya V. MR imaging of common and uncommon large pelvic masses. RadioGraphics2003; 23:403 -424[Abstract/Free Full Text]
  7. Metz CE. ROC methodology in radiologic imaging. Invest Radiol 1986; 21:720 -733[Medline]
  8. Metz CE. Some practical issues of experimental design and data analysis in radiological ROC studies. Invest Radiol1989; 24:234 -245[Medline]
  9. Scoutt LM, McCarthy SM, Lange R, Bourque A, Schwartz PE. MR evaluation of clinically suspected adnexal masses. J Comput Assist Tomogr 1994; 18:609 -618[Medline]
  10. Troiano RN, Lazzarini KM, Scoutt LM, Lange RC, Flynn SD, McCarthy S. Fibroma and fibrothecoma of the ovary: MR imaging findings. Radiology 1997;204 : 795-798[Abstract/Free Full Text]
  11. Ha HK, Baek SY, Kim SH, Kim HH, Chung EC, Yeon KM. Krukenberg's tumor of the ovary: MR imaging features. AJR1995; 164:1435 -1439[Abstract/Free Full Text]
  12. Outwater EK, Siegelman ES, Kim B, Chiowanich P, Blasbalg R, Kilger A. Ovarian Brenner tumors: MR imaging characteristics. Magn Reson Imaging 1998; 16:1147 -1153[CrossRef][Medline]
  13. Togashi K, Nishimura K, Nakano Y, et al. Cystic pedunculated leiomyomas of the uterus with unusual CT manifestations. J Comput Assist Tomogr 1986; 10:642 -644[Medline]
  14. Yoshitake T, Asayama Y, Yoshimitsu K, et al. Bilateral ovarian leiomyomas: CT and MRI features. Abdom Imaging2005; 30:117 -119[Medline]
  15. Kim JC, Kim SS, Park JY. "Bridging vascular sign" in the MR diagnosis of exophytic uterine leiomyoma. J Comput Assist Tomogr 2000; 24:57 -60[CrossRef][Medline]
  16. Mittl RL Jr, Yeh IT, Kressel HY. High-signal-intensity rim surrounding uterine leiomyomas on MR images: pathologic correlation. Radiology 1991;180 : 81-83[Abstract/Free Full Text]
  17. Foshager MC, Walsh JW. CT anatomy of the female pelvis: a second look. RadioGraphics 1994;14 : 51-64[Abstract]
  18. Lee JH, Jeong YK, Park JK, Hwang JC. "Ovarian vascular pedicle" sign revealing organ of origin of a pelvic mass lesion on helical CT. AJR 2003;181 : 131-137[Abstract/Free Full Text]
  19. Rebner M, Gross BH, Korobkin M, Ruiz J. CT appearance of right gonadal vein. J Comput Assist Tomogr1989; 13:460 -462[Medline]
  20. Moncada R, Reynes C, Churchill R, Love L. Normal vascular anatomy of the abdomen on computed tomography. Radiol Clin North Am 1979; 17:25 -37[Medline]
  21. Rozenblit AM, Ricci ZJ, Tuvia J, Amis ES Jr. Incompetent and dilated ovarian veins: a common CT finding in asymptomatic parous women. AJR 2001; 176:119 -122[Abstract/Free Full Text]
  22. Umeoka S, Koyama T, Togashi K, Kobayashi H, Akuta K. Vascular dilatation in the pelvis: identification with CT and MR imaging. RadioGraphics 2004;24 : 193-208[Abstract/Free Full Text]
  23. Hu H, He HD, Foley WD, Fox SH. Four multidetector-row helical CT: image quality and volume coverage speed. Radiology2000; 215:55 -62[Abstract/Free Full Text]

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Am. J. Roentgenol.Home page
M. Hirakawa, K. Yoshimitsu, D. Kakihara, H. Irie, Y. Asayayama, K. Ishigami, and H. Honda
Detection of the Gonadal Veins in the Diagnosis of Transposed Ovaries in Patients with Cervical Carcinoma: A Useful Sign on MDCT
Am. J. Roentgenol., June 1, 2007; 188(6): 1564 - 1567.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Asayama, Y.
Right arrow Articles by Honda, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Asayama, Y.
Right arrow Articles by Honda, H.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Hotlight (NEW!)
Right arrow
What's Hotlight?


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS