Radiology
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 Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
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 Hricak, H.
Right arrow Articles by Powell, C. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hricak, H.
Right arrow Articles by Powell, C. B.
(Radiology. 2000;214:39-46.)
© RSNA, 2000


Genitourinary Imaging

Complex Adnexal Masses: Detection and Characterization with MR Imaging-Multivariate Analysis1

Hedvig Hricak, MD, PhD, Min Chen, MD, Fergus V. Coakley, MB, BCh, Karen Kinkel, MD, Kyle K. Yu, MD, Gregory Sica, MD, Peter Bacchetti, PhD and C. Bethan Powell, MD

1 From the Departments of Radiology (H.H., M.C., F.V.C., K.K., K.K.Y., G.S.), Epidemiology and Biostatistics (P.B.), and Gynecologic Oncology (C.B.P.), University of California-San Francisco, 505 Parnassus Ave, San Francisco, CA 94143-0628. Received January 12, 1999; revision requested March 5; revision received April 6; accepted May 4. Address reprint requests to H.H.


    Abstract
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 References
 
PURPOSE: To evaluate the accuracy of magnetic resonance (MR) imaging in the detection and characterization of complex adnexal masses, with particular reference to the findings predictive of malignancy, role of gadolinium-enhanced contrast material, and observer variability.

MATERIALS AND METHODS: Preoperative MR imaging of the pelvis was performed in 128 consecutive patients with clinically or ultrasonographically detected complex adnexal masses. Histopathologic examination demonstrated 187 masses, 96 of which were malignant. MR imaging studies were prospectively and independently reviewed by two radiologists, one of whom reevaluated the studies after a 6-month interval. The predictive value of MR imaging findings was determined with multivariate logistic regression analysis. The value of gadolinium enhancement was assessed by using receiver operating characteristic analysis. Inter- and intraobserver variabilities were assessed by using weighted {kappa} statistics.

RESULTS: Gadolinium-enhanced MR imaging depicted 176 (94%) of 187 adnexal masses, with an overall accuracy for the diagnosis of malignancy of 93%. The MR imaging findings that were most predictive of malignancy were necrosis in a solid lesion (odds ratio, 107) and vegetations in a cystic lesion (odds ratio, 40). Use of gadolinium-based contrast material contributed significantly to lesion characterization. Interobserver ({kappa}, 0.79–0.85) and intraobserver ({kappa}, 0.84–0.86) agreement were excellent.

CONCLUSION: Gadolinium-enhanced MR imaging is highly accurate in the detection and characterization of complex adnexal masses, with excellent inter- and intraobserver agreement.

Index terms: Endometriosis, 852.3192 • Ovary, cysts, 852.311 • Ovary, neoplasms, 852.30, 852.323 • Pelvis, MR, 813.121411, 813.121415 • Receiver operating characteristic (ROC) curve • Teratoma, 852.313


    Introduction
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 References
 
The presence of an adnexal mass is one of the leading indications for gynecologic surgery. In the United States, 5%–10% of women will undergo surgery for a suspected adnexal mass during their lifetime, leading to 160,000–289,000 hospitalizations annually (1,2). A common misconception is that all large (>5-cm) adnexal masses, whether they are detected clinically or ultrasonographically, require resection and that further imaging characterization is superfluous. This belief ignores the importance of preoperative knowledge of the likely diagnosis in guiding subspecialty referral and surgical planning.

The main goal of imaging in the evaluation of an adnexal mass is the detection of malignancy (1). The standard of care for a suspected malignant adnexal mass is staging laparotomy with tumor debulking, which is performed preferably by an oncologic gynecologist (2). Ultrasonography (US) is the primary imaging modality for the assessment and characterization of adnexal masses, and the US features that indicate benignity are well established (312). However, the reported specificity of US for the diagnosis of benignity varies from 60% to 98%. In particular, as many as 20% of adnexal lesions in premenopausal women are classified as indeterminate by using US, even when they are interpreted in conjunction with clinical findings and CA-125 (ovarian cancer antigen) levels (13).

MR imaging has been shown to have potential in the characterization of adnexal masses: The results of two studies (14,15) demonstrated that MR imaging with gadolinium-based contrast material enhancement is superior to US. The tailored use of MR imaging in the evaluation of pelvic masses is also cost-effective (13,16). However, in these studies, a large number of patients were not examined and detailed multivariate analysis of MR imaging features was not performed. In addition, neither observer variability nor the role of intravenous gadolinium-based contrast material administration has been closely investigated. We undertook this study to further evaluate the accuracy of MR imaging in the detection and characterization of complex adnexal masses. In particular, we wished to determine which findings are most predictive of malignancy, assess the value of intravenous gadolinium-based contrast material administration, and assess inter- and intraobserver variabilities.


    MATERIALS AND METHODS
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 References
 
Patients
This was a prospective cross-sectional study. Between April 1, 1993, and May 30, 1996, 174 consecutive patients (age range, 18–83 years; mean age, 53 years) with clinically or US-depicted adnexal masses were referred for pelvic MR imaging from the gynecologic oncology clinic at our institution. In all cases, the adnexal masses were considered to be either indeterminate or possibly malignant after complete gynecologic and US assessment, which included a full medical history and clinical examination, full gynecologic examination, and appropriate laboratory tests such as CA-125 analysis.

MR imaging was considered to be clinically indicated for the evaluation of an adnexal lesion in all cases. None of the patients had contraindications to MR imaging. Of 174 patients, the 128 women who subsequently underwent surgery (laparoscopy or laparotomy) formed the study population. At surgery, 187 adnexal masses were found. The time interval between MR imaging and surgery was less than 1 month in 90 patients and between 1 and 2 months in 38 patients.

MR Imaging Technique
MR imaging was performed by using a 1.5-T MR imaging system (Signa; GE Medical Systems, Milwaukee, Wis) and either a body coil (n = 23) or pelvic phased-array coil (n = 105). Immediately before MR imaging, all patients were given 1 mg of intramuscular glucagon (Lilly, Indianapolis, Ind). None of the patients had contraindications to the administration of glucagon. The following images were obtained:

1. Sagittal T2-weighted fast spin-echo localizer images (repetition time msec/echo time msec, 4,000/102 [effective]).

2. Sagittal and transverse T2-weighted fast spin-echo images from the symphysis pubis to the aortic bifurcation (4,000–5,000/102 [effective]; echo-train length, eight; section thickness, 5 mm; intersection gap, 1 mm; field of view, 24 cm; four signals acquired and a 256 x 256 matrix used with the body coil and two signals acquired, a 512 x 256 matrix, and anterior and posterior spatial saturation bands used with the pelvic phased-array coil).

3. Transverse T1-weighted spin-echo images from the symphysis pubis to the aortic bifurcation (500–700/12; section thickness, 5–8 mm; intersection gap, 1–2 mm; field of view, 24 cm; one signal acquired; matrix, 256 x 192; use of respiratory compensation).

4. Optional transverse T1-weighted spin-echo images through any lesion with high T1 signal intensity by using the same parameters as those described above but with the addition of frequency-selective fat suppression. This sequence was performed when the supervising radiologist noted a lesion with high T1 signal intensity. Signal loss in the high-signal-intensity area of the lesion was considered to be diagnostic of fat in a cystic teratoma (17,18) (Fig 1).



View larger version (143K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1a. Right ovarian cystic teratoma (demoid tumor) in a 56-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a well-defined encapsulated right adnexal mass (asterisk) with high signal intensity. (b) On the transverse T1-weighted spin-echo MR image (500/17) with frequency-selective fat saturation, the mass (asterisk) has low signal intensity, which confirms the presence of fat. The appearances of this mass are typical of a dermoid tumor.

 


View larger version (126K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1b. Right ovarian cystic teratoma (demoid tumor) in a 56-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a well-defined encapsulated right adnexal mass (asterisk) with high signal intensity. (b) On the transverse T1-weighted spin-echo MR image (500/17) with frequency-selective fat saturation, the mass (asterisk) has low signal intensity, which confirms the presence of fat. The appearances of this mass are typical of a dermoid tumor.

 
5. Incremental precontrast transverse T1-weighted spin-echo images from the aortic bifurcation to the renal hila by using the body coil (500–700/12; section thickness, 5–8 mm; intersection gap, 1–2 mm; field of view, 24 cm; two signals acquired; matrix, 256 x 192; use of respiratory compensation).

6. Postcontrast transverse T1-weighted spin-echo images from the symphysis pubis to the aortic bifurcation after intravenous injection of 0.1 mmol/kg gadopentetate dimeglumine (Magnevist; Berlex Laboratories, Wayne, NJ) by using the same parameters as those used for precontrast T1-weighted imaging.

MR Image Analysis
The MR imaging findings were compared with the histopathologic findings, which were the standard of reference. Three separate MR image interpretations were recorded: (a) the formal report issued at the time of the MR imaging study by a senior radiologist (H.H.), (b) a separate independent retrospective reading by a junior radiologist (M.C.), and (c) a second reading by the senior radiologist at least 6 months after the first reading; this was done to evaluate intraobserver variability.

The senior radiologist had more than 10 years experience in pelvic MR imaging. The junior radiologist had 1 year of experience in pelvic MR imaging. The initial reading by the senior radiologist was performed with knowledge of all available clinical and US findings to optimize patient care. For the single reading of the junior radiologist and the second reading of the senior radiologist, the readers were aware that the patients were being evaluated for a possible adnexal lesion, but they were unaware of the other clinical or radiologic findings. Data were entered on a standardized form that was developed for the study.

We used the following previously established primary MR imaging findings to diagnose adnexal mass malignancy (19): mass size larger than 4 cm, presence of masses bilaterally, mass predominantly solid, necrosis in a solid lesion, and cystic lesion with wall or septal thickness greater than 3 mm or papillary projections. In addition, the following previously established (19) secondary MR imaging findings were used to diagnose adnexal mass malignancy: ascites, peritoneal metastasis, and adenopathy. The readers assessed each of these specific MR imaging findings.

A lesion was classified as malignant when at least two primary criteria were present or one primary and one ancillary finding were present. Each reader rated the conspicuity of each finding on nonenhanced and contrast material–enhanced images on a 1–5 scale, where 1 was extremely conspicuous and 5 was barely perceptible. For each MR examination, the readers estimated the likelihood that each of these findings was present by using a 0%–100% scale, where 0% was definitely absent and 100% was definitely present. Each reader also gave an overall impression of the likelihood of malignancy by using the same 0%–100% rating scale. Nonenhanced T1- and T2-weighted images and contrast-enhanced T1-weighted images were evaluated separately for lesion detection and characterization; the senior reader performed this detailed review at the 6-month delayed reading only.

Statistical Analyses
Multivariate logistic regression analysis was used to assess the predictive value of the presence of the five primary and three ancillary MR imaging findings used to assess for malignancy. The analysis was performed by both readers and by using nonenhanced and contrast-enhanced images. The outcome variable was the presence of malignancy at histopathologic examination. For logistic regression analysis, these results were dichotomized so that scores of greater than 60% were rated as "finding present," whereas scores of 60% or less were rated as "finding absent"; the choice of 60% as a threshold was based on the review of receiver operating characteristic curve analysis. Masses with a presumptive diagnosis of mature teratoma were excluded from MR image feature analysis.

The findings that were found to be statistically significant by using univariate analysis were entered into multivariate models to gauge their independent predictive value and determine which combination of findings would be most predictive of malignancy. The results were expressed as odds ratios of malignancy when a specific MR imaging finding was rated as definitely present compared with when it was rated as definitely absent. Descriptive statistical values, including accuracy, sensitivity, specificity, positive predictive value, and negative predictive value, were determined for each MR imaging finding. The pooled results of both readers were used to analyze the pre- and postexamination probabilities and determine the rates of detection with the nonenhanced and contrast-enhanced sequences. The statistical significance of differences in accuracies, sensitivities, and specificities was determined by using the McNemar test.

The areas under the receiver operating characteristic curves (Az) obtained by each reader at interpretation of both nonenhanced and contrast-enhanced images, as well as the asymptotic CIs, were calculated, and the statistical significance of the differences in these values between readers were determined by using permutation tests. The interobserver agreement on MR image interpretation between the senior radiologist and junior radiologist and the intraobserver agreement of the senior radiologist were quantified by using weighted {kappa} statistics; a {kappa} value of less than 0.40 was considered to represent poor agreement; 0.40–0.80, good agreement; and greater than 0.80, excellent agreement. The analyses were carried out by using Statistical Analysis System (SAS Institute, Cary, NC), Strata (Computing Resource Center, Santa Monica, Calif), and S-Plus (StatSci, Seattle, Wash) software packages.


    RESULTS
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 References
 
Histopathologic Findings
Of the 187 adnexal masses found in the 128 patients, 91 were benign and 96 were malignant. The histopathologic diagnoses of the 187 lesions are detailed in Table 1.


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

 
TABLE 1. Histopathologic Diagnoses in 187 Adnexal Masses
 
Lesion Detection at MR Imaging
On the nonenhanced images, 83 (91%) of 91 benign lesions and 89 (93%) of 96 malignant lesions were detected at MR imaging, with an overall detection rate of 92%. On the contrast-enhanced images, 85 (93%) of 91 benign lesions and 91 (95%) of 96 malignant lesions were detected, with an overall detection rate of 94%. The differences in the rate of detection of benign and malignant lesions between nonenhanced and contrast-enhanced images were not significant.

Eleven lesions—six benign and five malignant—were not detected on either the nonenhanced or contrast-enhanced images. The benign lesions that were not detected were three peritubal cysts, one endometrioma, one ovarian hyperthecosis, and one hydrosalpinx. All of the undetected benign lesions were smaller than 2 cm in diameter. The malignant lesions that were not detected were two bilateral clear cell ovarian carcinomas that were mistaken for bowel loops, two bilateral adnexal malignancies that were misinterpreted as single large unilateral masses (Fig 2), and one papillary serous adenocarcinoma (2 cm in maximum dimension).



View larger version (147K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2a. Confluent bilateral ovarian endometrioid carcinoma, which was not appreciated bilaterally at MR imaging in a 51-year-old-woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a large complex cystic and solid pelvic mass (arrows). (b) Transverse T1-weighted spin-echo MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates enhancement in the solid components (asterisk) and septa within the mass. These features were more conspicuous after contrast material administration. (c) Sagittal T2-weighted fast spin-echo MR image (4,000/90) demonstrates fluid-fluid levels (arrows) in the cystic components of the mass. These levels are barely perceptible in a and b.

 


View larger version (163K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2b. Confluent bilateral ovarian endometrioid carcinoma, which was not appreciated bilaterally at MR imaging in a 51-year-old-woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a large complex cystic and solid pelvic mass (arrows). (b) Transverse T1-weighted spin-echo MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates enhancement in the solid components (asterisk) and septa within the mass. These features were more conspicuous after contrast material administration. (c) Sagittal T2-weighted fast spin-echo MR image (4,000/90) demonstrates fluid-fluid levels (arrows) in the cystic components of the mass. These levels are barely perceptible in a and b.

 


View larger version (146K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2c. Confluent bilateral ovarian endometrioid carcinoma, which was not appreciated bilaterally at MR imaging in a 51-year-old-woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a large complex cystic and solid pelvic mass (arrows). (b) Transverse T1-weighted spin-echo MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates enhancement in the solid components (asterisk) and septa within the mass. These features were more conspicuous after contrast material administration. (c) Sagittal T2-weighted fast spin-echo MR image (4,000/90) demonstrates fluid-fluid levels (arrows) in the cystic components of the mass. These levels are barely perceptible in a and b.

 
Lesion Characterization at MR Imaging
Sixty-eight of 91 lesions (75%; 95% CI: 64%, 83%) were correctly characterized as benign on the nonenhanced images, and 72 of 91 (79%; 95% CI: 69%, 87%) were correctly characterized as benign on the contrast-enhanced images (not significant). Eighty-three of 96 masses (86%; 95% CI: 78%, 92%) were correctly characterized as malignant on the nonenhanced images, and 91 of 96 (95%; 95% CI: 88%, 98%) were correctly characterized as malignant on the contrast-enhanced images (P <.01). The receiver operating characteristic curves for the senior reader are illustrated in Figure 3. Diagnostic test statistics for the senior reader and junior reader interpretations of both the nonenhanced and enhanced images are listed in Table 2, and the pre- and postexamination probabilities of malignancy are listed in Table 3.



View larger version (25K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 3. Receiver operating characteristic curves of the senior reader illustrate the comparison of the diagnostic performances of nonenhanced T1- and T2-weighted images (dotted line) and of pre- and post-gadolinium-enhanced images (solid line) in the prediction of malignancy of an adnexal lesion. The contrast-enhanced images were significantly more accurate than the nonenhanced images (P < .001) in the prediction of malignancy. The addition of T2-weighted imaging to contrast-enhanced T1-weighted imaging did not increase accuracy over contrast-enhanced imaging alone. The Az value for the T1- and T2-weighted images was 0.91; the pre- and post-gadolinium-enhanced images, 0.96; and the T1- and T2-weighted images combined with the pre- and post-gadolinium-enhanced images (dashed line), 0.98.

 

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

 
TABLE 2. Accuracy of MR Imaging in Characterizing Complex Adnexal Masses as Benign or Malignant
 

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

 
TABLE 3. Postexamination Probabilities of Malignancy in 187 Adnexal Masses
 
Gadolinium-enhanced images significantly improved lesion characterization. The benefit of contrast material appeared to be improved conspicuity of the morphologic features of the lesions. The average ratings of conspicuity of the individual MR imaging criteria used to diagnose malignancy on the nonenhanced and contrast-enhanced images are shown in Table 4. The conspicuity ratings were significantly higher on the gadolinium-enhanced images (P <.01) for classification of a predominantly solid or cystic lesion, determination of wall and septal thicknesses, detection of vegetations in a cystic lesion (Fig 4), and identification of necrosis in a solid lesion (Fig 5). The use of T2-weighted imaging in addition to pre- and postcontrast T1-weighted imaging did not further improve lesion characterization. There was good to excellent interobserver agreement between the readings of the experienced and less experienced readers: {kappa} ranged from 0.79 with the nonenhanced images to 0.85 with all the MR imaging sequences combined. Similarly, there was excellent intraobserver agreement ({kappa}, 0.84–0.86).


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

 
TABLE 4. Conspicuity Ratings for MR Imaging Criteria Used to Diagnose Malignancy
 


View larger version (109K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4a. Large papillary serous adenocarcinoma of the ovary in a 56-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a right cystic adnexal lesion (asterisk) without clearly evident suspicious features. (b) Transverse spin-echo T1-weighted MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates an enhancing vegetation (arrow) in the lesion, which indicates malignancy.

 


View larger version (137K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4b. Large papillary serous adenocarcinoma of the ovary in a 56-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a right cystic adnexal lesion (asterisk) without clearly evident suspicious features. (b) Transverse spin-echo T1-weighted MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates an enhancing vegetation (arrow) in the lesion, which indicates malignancy.

 


View larger version (157K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 5a. Bilateral ovarian metastatic recurrence of colonic adenocarcinoma, in a 67-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates bilateral adnexal masses (arrows) with mild internal heterogeneity. (b) Transverse T1-weighted spin-echo MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates irregular areas of central necrosis (arrows) within the masses.

 


View larger version (178K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 5b. Bilateral ovarian metastatic recurrence of colonic adenocarcinoma, in a 67-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates bilateral adnexal masses (arrows) with mild internal heterogeneity. (b) Transverse T1-weighted spin-echo MR image (500/17) obtained after the intravenous administration of gadolinium-based contrast material demonstrates irregular areas of central necrosis (arrows) within the masses.

 
Table 5 shows the results of univariate and multivariate logistic regression analyses of primary and secondary MR imaging criteria. The primary criteria found to be the most significant predictors of malignancy were the presence of vegetations or solid components in a cystic lesion and the presence of necrosis in a solid lesion. The results of stepwise multivariate analysis indicated that, in addition to these primary criteria, the presence of the ancillary findings of ascites or peritoneal metastasis further increased the likelihood of malignancy (Fig 6). The likelihood of malignancy also increased with patient age, although this was a less important predictor of malignancy.


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

 
TABLE 5. Univariate and Multivariate Logistic Regression Analyses of MR Imaging Criteria
 


View larger version (162K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 6. Bilateral ovarian serous cystadenocarcinoma in an 18-year-old woman. Sagittal T2-weighted fast spin-echo MR image (4,000/85.2) demonstrates a large complex cystic and solid pelvic mass (asterisk) surrounded by ascites. Partially confluent peritoneal nodules (arrow) also are evident. Ascites and peritoneal nodules are consistent with peritoneal carcinomatosis.

 

    DISCUSSION
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 References
 
The pretreatment determinations of the location, size, and likelihood of malignancy of a lesion are becoming increasingly important as treatment options for adnexal masses become more sophisticated and more patient specific. In practice, US is the primary imaging modality for the evaluation of adnexal masses. The addition of patient demographic and laboratory data such as CA-125 results to US findings improves characterization, especially in postmenopausal patients. However, the evaluation of adnexal masses in premenopausal women remains a dilemma. There can be multiple causes of elevated CA-125 levels in a premenopausal patient, including endometriosis and pelvic inflammatory disease.

MR imaging is considered to be a problem-solving technique in the assessment of adnexal masses. Gadolinium-enhanced MR imaging appears to be more accurate than US in the assessment of adnexal masses (14,15). Nonenhanced MR imaging, contrast-enhanced computed tomography, and US all have similar accuracy (15,2022). The results of our prospective study in a large patient population confirm previous reports suggesting that MR imaging is helpful in the evaluation of adnexal pathologic entities (14,15,19). Our findings demonstrate that gadolinium-enhanced MR imaging has a high rate of depiction of both benign (93%) and malignant (95%) lesions. Potential problems in lesion detection with MR imaging include small (<2-cm) lesion size and occasional difficulty in determining whether a large adnexal mass is unilateral or bilateral. The results of our study of lesion characterization are similar to previously published data (14,15,19). It is noteworthy that the results of our analysis of pre- and postexamination probabilities (Table 3) showed that MR imaging is most useful in confirming malignancy in complex adnexal masses. The postexamination probability of malignancy after a positive contrast-enhanced MR imaging examination was 94%, whereas the postexamination probability of malignancy after a negative contrast-enhanced MR imaging examination was 19%, which we believe is relatively high.

Our study results showed that contrast-enhanced MR imaging is significantly more accurate in lesion characterization than nonenhanced MR imaging. The improved characterization is due to greater conspicuity of the critical MR imaging findings, including the presence of solid components (or vegetations) in a cystic lesion and necrosis in a solid lesion. It should be noted that cystic teratomas (ie, dermoid cysts) are an exception to the conclusion that solid components in a cystic lesion imply malignancy. The presence of fat in a cystic adnexal lesion is diagnostic of a cystic teratoma, even if solid components (eg, Rokitansky nodules) also are present (17,18). Therefore, we excluded fat-containing lesions from our MR image feature analysis. The demonstration of fat requires both standard and fat-suppressed T1-weighted imaging, because the latter helps to differentiate fat from blood products as a cause of the high T1 signal intensity (2325). Interestingly, the results of our characterization analysis showed that T2-weighted imaging does not add a significant diagnostic benefit to contrast-enhanced T1-weighted imaging. However, T2-weighted images may be helpful in the characterization of ovarian fibromas (26) (Fig 7), and we continue to obtain such images when evaluating adnexal masses.



View larger version (127K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 7a. Right ovarian fibroma, which was discovered during pelvic US performed for the evaluation of infertility in a 33-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a well-defined solid mass (arrow) with low signal intensity in the right ovary. (b) On the transverse T2-weighted fast spin-echo MR image (4,000/90), the mass (arrow) has low signal intensity, which strongly suggests a diagnosis of fibroma.

 


View larger version (135K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 7b. Right ovarian fibroma, which was discovered during pelvic US performed for the evaluation of infertility in a 33-year-old woman. (a) Transverse T1-weighted spin-echo MR image (500/17) demonstrates a well-defined solid mass (arrow) with low signal intensity in the right ovary. (b) On the transverse T2-weighted fast spin-echo MR image (4,000/90), the mass (arrow) has low signal intensity, which strongly suggests a diagnosis of fibroma.

 
One objective of this study was to determine which MR imaging findings are the most predictive of malignancy in an adnexal mass. The results of multivariate logistic regression analysis indicated that the presence of vegetations in a cystic lesion and the presence of necrosis in a solid lesion were the two most significant predictors. These findings are consistent with the results of a logistic regression analysis of US features that helped to distinguish benign from malignant ovarian masses, in which it was found that the presence of a solid component was the single most statistically significant predictor of malignancy (27).

In our study, although the combination of size larger than 4 cm and thickness of wall or septa greater than 3 mm also was significant in predicting malignancy, there was no improvement with the use of these criteria compared with the use of vegetation and necrosis as criteria. The results also indicated that lesion size, when combined with other imaging findings, does not further contribute to the prediction of malignancy (Fig 8). This appears to be discordant with the results of US-based studies, which have shown that lesion size larger than 4 cm substantially increases the likelihood of malignancy (28). The discrepancy is probably due to differences in patient selection. Most US studies include the evaluation of all adnexal masses and are often based on consecutive patients seen in primary care clinics. Such studies have a correspondingly high proportion of small benign lesions: Typically, 80% of the lesions are benign, and the average lesion is smaller than 4 cm. Our study included only patients referred from a gynecologic oncology clinic who had complex adnexal lesions, that is, adnexal masses that were not clearly benign after complete clinical and US assessment. It is likely that once small and clearly benign cystic lesions are excluded, size does not have a further role in lesion characterization. This finding suggests that lesion size can be used to aid in characterization at the initial US assessment but should not be used as a discriminator when an ultrasonographically suspicious or inconclusive lesion is referred for evaluation on the basis of MR imaging findings.



View larger version (147K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 8. Bilateral ovarian mucinous cystadenomas in a 41-year-old woman. Transverse T2-weighted fast spin-echo MR image (5,000/90) demonstrates large bilateral adnexal lesions (asterisks), which are predominantly cystic. The lesions are thin walled with thin internal septa and no papillary projections. The findings correctly suggest benignity, despite the large size of the lesions.

 
In one previous study (21) with a small number of patients, there was low to moderate interobserver agreement ({kappa}, 0.41) between two independent radiologists in the assessment of ovarian malignancy. In contrast, our study results demonstrated excellent interobserver agreement between two independent radiologists and excellent intraobserver agreement between the initial and 6-month delayed readings of the senior reader. The very high degree of intraobserver agreement is particularly noteworthy, because the second reading was performed without knowledge of the other clinical and radiologic findings, which were known at the initial reading. The lack of a difference between the two readings, even in the absence of clinical and US data at the second reading, indicates that the MR imaging findings used for characterization are objective and robust criteria. This further confirms that MR imaging is a reliable diagnostic technique for the characterization of adnexal masses.

A potential criticism of our study is that the patient selection was biased, because all the patients had adnexal masses that were considered to be of sufficient concern at clinical or US evaluation to merit assessment at the gynecologic oncology clinic. However, despite this selection bias, nearly half (91 of 187) of the adnexal masses resected were benign; this indicated a wide spectrum of pathologic entities in our study group. In addition, this approach reflects the real-life use of MR imaging, which is reserved as a problem-solving modality. MR imaging is not used as the primary imaging tool in the evaluation of suspected adnexal masses.

Imaging algorithms are an essential part of clinical practice guidelines. On the basis of established practice and a review of the literature (312), we recommend that US remain the primary imaging modality for the evaluation of a clinically suspected adnexal mass. When the results of US evaluation are indeterminate, MR imaging is a cost-effective next step (13). Gadolinium-enhanced MR imaging is highly accurate in the detection and characterization of complex adnexal masses, with excellent inter- and intraobserver agreement. Gadolinium-based contrast material administration is recommended because it increases the conspicuity of findings that are predictive of malignancy. Our study results further validate the described primary and secondary MR imaging findings of adnexal malignancy (19) and show that MR imaging can be recommended as a reliable and reproducible modality in the assessment of complex adnexal masses.


    Footnotes
 
Author contributions: Guarantor of integrity of entire study, H.H.; study concepts, C.B.P., H.H., G.S.; study design, C.B.P., H.H., K.K.Y.; definition of intellectual content, H.H., K.K.Y., F.V.C.; literature research, K.K.Y., K.K.; clinical studies, C.B.P., H.H., M.C.; data acquisition, K.K.Y., M.C.; data analysis, K.K.Y., M.C., P.B.; statistical analysis, P.B.; manuscript preparation, H.H., K.K.Y., F.V.C.; manuscript editing, F.V.C.; manuscript review, C.B.P., H.H., K.K.Y.


    References
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 References
 

  1. Curtin JP. Management of the adnexal mass. Gynecol Oncol 1994; 55:S42-S46.[Medline]
  2. NIH consensus conference. Ovarian cancer: screening, treatment, and follow-up—NIH consensus development panel on ovarian cancer. JAMA 1995; 273:491-497.[Abstract]
  3. Gadducci A, Capriello P, Bartolini T, et al. The association of ultrasonography and CA-125 test in the preoperative evaluation of ovarian carcinoma. Eur J Gynaecol Oncol 1988; 9:373-376.[Medline]
  4. Salem S, White LM, Lai J. Doppler sonography of adnexal masses: the predictive value of the pulsatility index in benign and malignant disease. AJR 1994; 163:1147-1150.[Abstract/Free Full Text]
  5. Kawai M, Kikkawa F, Ishikawa H, et al. Differential diagnosis of ovarian tumors by transvaginal color-pulse Doppler sonography. Gynecol Oncol 1994; 54:209-214.[Medline]
  6. Levine D, Feldstein VA, Babcook CJ, Filly RA. Sonography of ovarian masses: poor sensitivity of resistive index for identifying malignant lesions. AJR 1994; 162:1355-1359.[Abstract/Free Full Text]
  7. DePriest PD, Varner E, Powell J, et al. The efficacy of a sonographic morphology index in identifying ovarian cancer: a multi-institutional investigation. Gynecol Oncol 1994; 55:174-178.[Medline]
  8. Stein SM, Laifer-Narin S, Johnson MB, et al. Differentiation of benign and malignant adnexal masses: relative value of gray-scale, color Doppler, and spectral Doppler sonography. AJR 1995; 164:381-386.[Abstract/Free Full Text]
  9. Rehn M, Lohmann K, Rempen A. Transvaginal ultrasonography of pelvic masses: evaluation of B-mode technique and Doppler ultrasonography. Am J Obstet Gynecol 1996; 175:97-104.[Medline]
  10. Tingulstad S, Hagen B, Skjeldestad FE, et al. Evaluation of a risk of malignancy index based on serum CA125, ultrasound findings and menopausal status in the pre-operative diagnosis of pelvic masses. Br J Obstet Gynaecol 1996; 103:826-831.[Medline]
  11. Buy JN, Ghossain MA, Hugol D, et al. Characterization of adnexal masses: combination of color Doppler and conventional sonography compared with spectral Doppler analysis alone and conventional sonography alone. AJR 1996; 166:385-393.[Abstract/Free Full Text]
  12. Valentin L. Gray scale sonography, subjective evaluation of the color Doppler image and measurement of blood flow velocity for distinguishing benign and malignant tumors of suspected adnexal origin. Eur J Obstet Gynecol Reprod Biol 1997; 72:63-72.[Medline]
  13. Aultman CJ, Feller JF, Jain KA, Dougherty RS, Alagoz T. MR imaging of sonographically indeterminate adnexal masses: cost-benefit study (abstr). Radiology 1995; 197(P):354.
  14. Medl M, Kulenkampff KJ, Stiskal M, Peters-Engl C, Leodolter S, Czembirek H. Magnetic resonance imaging in the preoperative evaluation of suspected ovarian masses. Anticancer Res 1995; 15:1123-1125.[Medline]
  15. Yamashita Y, Torashima M, Hatanaka Y, et al. Adnexal masses: accuracy of characterization with transvaginal US and precontrast and postcontrast MR imaging. Radiology 1995; 194:557-565.[Abstract/Free Full Text]
  16. Schwartz LB, Panageas E, Lange R, Rizzo J, Comite F, McCarthy S. Female pelvis: impact of MR imaging on treatment decisions and net cost analysis. Radiology 1994; 192:55-60.[Abstract/Free Full Text]
  17. Togashi K, Nishimura K, Itoh K, et al. Ovarian cystic teratomas: MR imaging. Radiology 1987; 162:669-673.[Abstract/Free Full Text]
  18. Muramatsu Y, Moriyama N, Takayasu K, Nawano S, Yamada T. CT and MR imaging of cystic ovarian teratoma with intracystic fat balls. J Comput Assist Tomogr 1991; 15:528-529.[Medline]
  19. Stevens SK, Hricak H, Stern JL. Ovarian lesions: detection and characterization with gadolinium-enhanced MR imaging at 1.5 T. Radiology 1991; 181:481-488.[Abstract/Free Full Text]
  20. Jain KA, Friedman DL, Pettinger TW, Alagappan R, Jeffrey RB, Jr, Sommer FG. Adnexal masses: comparison of specificity of endovaginal US and pelvic MR imaging. Radiology 1993; 186:697-704.[Abstract/Free Full Text]
  21. Buist MR, Golding RP, Burger CW, et al. Comparative evaluation of diagnostic methods in ovarian carcinoma with emphasis on CT and MRI. Gynecol Oncol 1994; 52:191-198.[Medline]
  22. Ghossain MA, Buy JN, Ligneres C, et al. Epithelial tumors of the ovary: comparison of MR and CT findings. Radiology 1991; 181:863-870.[Abstract/Free Full Text]
  23. 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]
  24. Yamashita Y, Torashima M, Hatanaka Y, et al. Value of phase-shift gradient-echo MR imaging in the differentiation of pelvic lesions with high signal intensity at T1-weighted imaging. Radiology 1994; 191:759-764.[Abstract/Free Full Text]
  25. Guinet C, Ghossain MA, Buy JN, et al. Mature cystic teratomas of the ovary: CT and MR findings. Eur J Radiol 1995; 20:137-143.[Medline]
  26. 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]
  27. Brown DL, Doubilet PM, Miller FH, et al. Benign and malignant ovarian masses: selection of the most discriminating gray-scale and Doppler sonographic features. Radiology 1998; 208:103-110.[Abstract/Free Full Text]
  28. Rulin MC, Preston AL. Adnexal masses in postmenopausal women. Obstet and Gynecol 1987; 70:578-581.[Medline]



This article has been cited by other articles:


Home page
RadiologyHome page
I. Thomassin-Naggara, M. Bazot, E. Darai, P. Callard, J. Thomassin, and C. A. Cuenod
Epithelial Ovarian Tumors: Value of Dynamic Contrast-enhanced MR Imaging and Correlation with Tumor Angiogenesis
Radiology, July 1, 2008; 248(1): 148 - 159.
[Abstract] [Full Text] [PDF]


Home page
ImagingHome page
S Ghattamaneni, M J Weston, and J A Spencer
Imaging in endometriosis
Imaging, December 1, 2007; 19(4): 345 - 368.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
S. Adusumilli, H. K. Hussain, E. M. Caoili, W. J. Weadock, J. P. Murray, T. D. Johnson, Q. Chen, and B. Desjardins
MRI of sonographically indeterminate adnexal masses.
Am. J. Roentgenol., September 1, 2006; 187(3): 732 - 740.
[Abstract] [Full Text] [PDF]


Home page
RadioGraphicsHome page
I. Imaoka, A. Wada, Y. Kaji, T. Hayashi, M. Hayashi, M. Matsuo, and K. Sugimura
Developing an MR Imaging Strategy for Diagnosis of Ovarian Masses
RadioGraphics, September 1, 2006; 26(5): 1431 - 1448.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Radiol.Home page
J A Spencer
A multidisciplinary approach to ovarian cancer at diagnosis
Br. J. Radiol., October 1, 2005; 78(Special_Issue_2): S94 - S102.
[Full Text] [PDF]


Home page
RadiologyHome page
K. Kinkel, Y. Lu, A. Mehdizade, M.-F. Pelte, and H. Hricak
Indeterminate Ovarian Mass at US: Incremental Value of Second Imaging Test for Characterization--Meta-Analysis and Bayesian Analysis
Radiology, July 1, 2005; 236(1): 85 - 94.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
A. Saini, R. Dina, G. A. McIndoe, W. P. Soutter, P. Gishen, and N. M. deSouza
Characterization of Adnexal Masses with MRI
Am. J. Roentgenol., March 1, 2005; 184(3): 1004 - 1009.
[Full Text] [PDF]


Home page
ImagingHome page
J A Spencer and M J Weston
Imaging in endometriosis
Imaging, June 1, 2003; 15(2): 63 - 71.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
S. A. A. Sohaib, A. Sahdev, P. V. Trappen, I. J. Jacobs, and R. H. Reznek
Characterization of Adnexal Mass Lesions on MR Imaging
Am. J. Roentgenol., May 1, 2003; 180(5): 1297 - 1304.
[Abstract] [Full Text] [PDF]


Home page
RadioGraphicsHome page
J. Szklaruk, E. P. Tamm, H. Choi, and V. Varavithya
MR Imaging of Common and Uncommon Large Pelvic Masses
RadioGraphics, March 1, 2003; 23(2): 403 - 424.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
M. J. McClure, M. Atri, M. A. Haider, and J. Murphy
Perineural Cysts Presenting as Complex Adnexal Cystic Masses on Transvaginal Sonography
Am. J. Roentgenol., December 1, 2001; 177(6): 1313 - 1318.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
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 Hricak, H.
Right arrow Articles by Powell, C. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hricak, H.
Right arrow Articles by Powell, C. B.