Evaluation of primary adnexal masses by 3T MRI: categorization with conventional MR imaging and diffusion-weighted imaging

From Jan 2010 to Jun 2012, 312 consecutive patients with clinically suspected adnexal diseases underwent 3.0 T MRI examinations before pelvic or laparoscopic surgery. The time interval between MRI evaluation and surgery was within 1 month. Patients with metastatic ovarian tumors (n = 32), recurrent diseases of known gynaecological malignancies (n = 55), previous treatment history (n = 30) and a lack of DWI-MRI (n = 3) were excluded. Patients with mature teratoma (n = 53) were also arbitrarily excluded because diagnosis is less challenging, as described in the literature [9]. Therefore, we retrospectively reviewed 139 patients (13–83 years of age; average age, 51.3 ± 17.1 years) with pathologically proven primary adnexal masses. The patient cohort group included 22 ovarian cysts, 33 endometriomas and 43 benign and 42 malignant tumors. Details of the patients are summarized in Table 1. Our institutional review board approved this study, and waivers of informed consent from all participants were granted.

All MRI examinations were performed on a 3.0-Tesla (3 T) system (Signa HD, General Medical Systems, GE, USA) equipped with an 8-channel cardiac array coil. The scan range was from the umbilicus level to the pubic symphysis in the caudocranial direction. For any larger lesion that could not be covered on axial imaging, a sagittal scanning sequence was performed to include as much of the entire lesion as possible. Routine MRI protocols were used for the assessment of adnexal masses, which included the following: axial fast spin-echo (FSE) T1-weighted images (T1WI), sagittal FSE T2WI and fat-suppressed T2WI (FS T2WI). A DWI-MRI sequence used an echo-planar imaging sequence with an array spatial sensitivity encoding technique. The parameter details of the T1WI MR protocol were: repetition time (TR), 460 ms; echo time (TE), 10 ms; NEX, 2; and thickness, 6.0 mm. The parameter details of the T2WI MR protocol were: TR, 2400 ms; TE, 85 ms; NEX, 1; and thickness, 6.0 mm. The parameter details of the FS T2WI MR protocol were: TR, 3160 ms; TE, 90 ms; NEX, 2; and thickness, 6.0 mm. The parameter details of the DWI-MRI MR protocol were: TR, 3500 ms; TE, 61 ms; NEX, 6; and thickness, 6.0 mm. and, the b value = 0 and 700 s/mm². A liver acquisition with volume acceleration (LAVA) sequence was used to perform contrast-enhanced pelvic imaging, and a power injector (Missouri Ulrich; Ulm, Germany) was used for injection of contrast material (Magnevist, Bayer Schering Pharma AG, Germany). The parameter details of the LAVA MR protocol were: TR, 3.4 ms; TE, 1.4 ms; NEX, 1; flip angle, 1.5; and band width, 125 kHz. Images were acquired at multiple phases of contrast medium enhancement in both sagittal and axial planes (precontrast sagittal and axial oblique and postcontrast at 20 seconds, 40 seconds, 60 seconds and 80 seconds in the axial plane and 120 seconds in the sagittal plane).

The MRI characteristics of each adnexal lesion were separately recorded according to the following items: 1) lesion components graded on a 5-point scale [1 = cystic; 2 = solid; 3 = cyst with septum; 4 = cyst with solid components (nodules); 5 = cyst with septum and solid components; 2) signal intensity compared with that of the outer myometrium on T1WI and T2WI graded on a 9-point scale (low or equal intensity on T1WI and high intensity = 1, low intensity = 2 and mixed signal = 3 on T2WI, high or equal intensity on T1WI and high intensity = 4, low intensity = 5 and mixed signal = 6 on T2WI, mixed signal on T1WI and low intensity = 7, high intensity = 8, and mixed signal intensity = 9 on T2WI) and 3) DWI-MRI signal graded on a 4-point scale (1 = low; 2 = intermediate; 3 = high; 4 = mixed). The low signals on DWI-MRI indicated that the signals of lesion were similar with the pelvic bone signal and the intermediate signals were similar with the outer myometrium. The high signals on DWI-MRI were like that of endometrium.

Commercially available software was used on a postprocessing workstation (GE Advantage workstation 4.3, General Electric Healthcare, Milwaukee, WI, USA) to calculate ADCs. Regions of interest (ROI) were drawn manually in both cystic and solid areas with no more than 3 sites in each lesion on b value = 700 DWI-MRI images. The round or elliptical circle were centrally placed in the targeted region with the area range of 160–220 mm². Only the lowest ADCs were used for subsequent statistical analysis. For any lesions which were not clearly depicted on DWI-MRI, then axial fat-suppressed T2WI images and dynamic contrast-enhanced images were also reviewed in order to help to define the small nodular components. ADCs were not available for small size (< 10 mm) in endometric cyst group (one case) or severe pulsative artefacts due to large size in benign tumors (three cases ≥ 100 mm) and malignant tumors (four cases ≥ 250 mm).

Two observers (Y. Z. H. and H.Z, with 15 and 6 years of experience in gynaecological imaging, respectively), who were blinded to the histological results independently analysed all of the MRI datasets of each participant on a Picture Archiving and Communication System terminal server. In patients with ≥ 1 lesions with different pathological type, all lesions were selected for further analysis. For interobserver discrepancies in the evaluation of adnexal lesions, consensus was achieved or a majority decision was obtained.

Most of ovarian cyst (18/22) (Figure 1) and endometrioma (27/33) appeared as cystic lesions. Most of the benign tumors appeared as lesions that were solid (14/43) or cyst with septa (14/43). A cystic component combined with a solid nodule (22/42) was the most common type in the malignant group. There were 15 solid lesions in benign and 7 solid lesions in malignant group (Figure 2). There was significant difference in signal between the benign and malignant tumor (P = 0.000). The MRI components within the 4 groups in 140 primary adnexal lesions are summarized in Table 4.

Most of ovarian cyst (13/22) showed as low/equal intensity on T1WI and mixed signal on T2WI. Most of endometrioma (17/33) appeared as high/equal intensity on T1WI and hyper intensity on T2WI. Accordingly, most of the benign (29/43) and malignant tumors (19/42) showed low/equal intensity on T1WI and hyper intensity on T2WI. The MRI signals between ovarian cyst and endometrioma and benign tumor gave statistically significant differences (P = 0.000, P = 0.000), while no difference was observed between ovarian cyst and malignant tumor (P = 0.965). There was a significant difference between the endometrioma and benign and malignant tumor (P = 0.000, P = 0.002). The signal difference between benign and malignant tumor also significantly differed (P = 0.008). The MRI signals of the lesions were not significantly different between the non-malignant (regarding the ovarian cyst, endometrioma and benign ovarian tumor as the whole category) and malignant lesions (P = 0.606). The MRI signal characteristics within the 4 groups are summarized in Table 5.

Most of the primary adnexal lesions (69/140) showed hyperintensity on DWI-MRI. Most of the malignant tumors (27/42) gave high signal in this series. The differences in DWI-MRI signals within each group were statistically significant except between endometrioma and malignant tumor (P = 0.546). However, the DWI-MRI signals of the lesions were significantly different between the non-malignant and malignant groups (P = 0.008). The DWI-MRI signals within the 4 groups are summarized in Table 6.

In our results, the highest ADC value was 2.47 ± 0.93 observed in ovarian cyst, while the lowest was 1.39 ± 0.62 in the malignant tumor (Table 1). The mean ADC value of ovarian cysts was higher than that of the other groups, although a significant difference between the ovarian cyst and benign tumors was not observed (P = 0.080). No significant differences were observed in the ADCs between the endometrioma and benign (P = 0.121), but a significant difference was observed between the benign and malignant tumor (P = 0.000) (Figure 3). There was also a significant difference between the non-malignant and malignant lesions (P = 0.000). In the 22 solid lesions in this sample (Figure 2), the mean ADCs between the benign and malignant tumors were not significantly different (P = 0.399).

Primary adnexal masses comprise a broad spectrum of diseases in which the aetiology is often difficult to determine by ultrasonography because of the similarity in the imaging appearances. With the advantage of excellent contrast resolution, MRI is a problem-solving modality for distinguishing benign from malignant ovarian tumors [12‐16].

We reported our single-centre preliminary experiences using 3.0 T MRI for evaluation of primary adnexal lesions in 139 subjects. With respect to baseline characteristics of primary adnexal lesions, when ovarian cyst and endometrioma were excluded, there was significant difference in maximum diameters of lesions and CA125 level between the primary ovarian benign and malignant tumors. CA125 level could be used as a reference standard for differentiating benign from malignant tumors [17], although some overlap between endometrioma and malignant tumors was observed.

Considering the components of lesions, our findings are in line with those of other studies that used conventional imaging and showed that complex structures were more often seen in ovarian tumors and there was more overlap in appearance between benign and malignant tumors [2, 18‐21]. In our series, except for ovarian cyst, the signal intensity in all primary ovarian lesions varied considerably, which would present a diagnostic challenge if conventional imaging only were used. The typical shading character (high signal on T1WI and low signal on T2WI) of endometrioma, as well described in the literature [22], does not often occur in this patient group. It has been reported that endometriosis is a precursor lesion of ovarian malignancies, particularly in endometrioid and clear-cell types [2, 23]. Considering this, caution is needed to precisely confirm the diagnosis of endometrioma, especially in cases with atypical imaging findings.

DWI-MRI is a functional imaging technique that is now widely applied for characterization of primary adnexal lesions and staging of ovary cancers [7, 9, 24, 25]. However, DWI-MRI in gynaecological adnexial masses must be carefully interpreted by diagnosticians because any normal structures could appear bright on high b-value images [26, 27]. Two studies reported that the areas of high signal intensity on DWI-MRI were observed more often in malignant than in benign tumors [7, 28]. In another study, the author concluded that the DWI-MRI signal was more related to the signal intensity of the fluid rather than to a histopathological component [29]. In our study, except for ovarian cyst, most parts of the primary adnexal lesions showed high signals on b = 700 DWI-MRI in both benign and malignant tumors. On the whole, there was significant difference in the DWI-MRI signal between non-malignant and malignant lesions, a finding that is inconsistent with that of a study by Fujii S et al. [30]. The possible explanation is that in their study, teratoma was included, which was different with our studied samples, may result in elevated numbers with high DWI-MRI signal in benign group. In one article, investigators stated that low T2 signal and low signal on DWI-MRI with a b-value of 1000 were the best criteria for predicting benignity [9]. However, we do not support this point of view. In our data, we found that few lesions with these characteristics were encountered, which would lead to limited application in a clinical situation.

In theory, as a result of high cell densities and abundant cellular membranes, the ADCs should be generally lower in cancerous tissue than in noncancerous tissue [8]. Even so, the application of ADCs in differentiating malignant from benign ovarian tumors remains a controversy [9, 28‐32]. The choice of b-values, varying pathologies and the number of studied samples all result in a wide divergence of reported ADCs for ovarian cystic and solid diseases. In our results, the highest ADC value was 2.47 ± 0.93 observed in ovarian cyst, while the lowest was 1.39 ± 0.62 in the malignant group. It is worth noting that the wide range of calculated ADCs in the benign group resulted in considerable overlap with those of the endometrioma and malignant tumor, although there was a statistically significant difference between the benign and malignant tumor (P = 0.000). This phenomenon reflects the more variable components of benign ovarian tumors. We excluded teratomas from further analysis because these lesions can be easily detected without any diagnostic challenge [9, 21, 29]. Thomassin NI et al. reported that the ADCs of the cystic component and of the solid component did not differ between malignant and benign adnexal masses [9]. However, in their study, the benign groups with measurable solid component ADCs mainly composed of rich collagen fibril cells obviously restricted the diffusion of water molecules and resulted in low ADCs, which was different with our study. In another study, the authors also declared that ADCs may not provide additional information for differentiating between benign and malignant tumors [29]. However, there were only 10 malignant cases in their research, which considerably limited the broader applicability of their conclusions. In addition, ovarian metastatic tumors were excluded in our patient selection, which is mostly different from the selection used in other reported studies [9, 28‐32]; therefore, our study sample may more accurately reflect the true features of ovarian masses.

We agree with the view of Takeuchi M et al. that some benign fibrous lesions also have lower ADCs with, ironically, no elevated signal on DWI-MRI [28]. However, the typical character of the low signal on T2WI allows easy differentiation of these benign lesions from malignant tumors. Considering the 22 solid lesions, however, differences in ADCs between benign and malignant types were not observed in this study. Bakir B et al. studied 37 patients with solid or predominantly solid adnexial masses who underwent DWI-MRI evaluation and disclosed that the ADCs of both malignant and benign adnexal lesions also did not show a significant difference [7]. To date, DWI-MRI and ADC evaluations of ovarian solid tumors have not been fully investigated. Because of the relatively small samples, these results are conservative and need to be verified in a large study.

We must acknowledge several limitations in our study. First, some authors have recommended that any lesion displaying a high T1 signal before the DWI sequence should be excluded to limit T1 contamination because the ADC value may increase linearly with decreasing protein concentrations [9, 33]. In this study, we did not exclude these lesions so that we could encompass different types of lesions as much as possible. However, we do think this influenced the DWI-MRI signal, which could not show the real restricted diffusion of the lesions. Second, the area of the ROI on which the ADCs were calculated was manually outlined. Lack of standardization in selecting ROI areas also may influence the final ADCs. Third, in our study, we compared our results using 3 T MRI with those of other studies that used 1.5 T MRI. Although Takeuchi M et al. reported that there was no significant difference between the ADC values obtained at 1.5 T and 3.0 T [28], a direct comparison between the two modalities may be still needed to clarify the true difference in ADC s.