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AJR 2005; 184:1004-1009
© American Roentgen Ray Society


Pictorial Essay

Characterization of Adnexal Masses with MRI

Ash Saini1, Roberto Dina2, G. Angus McIndoe3, W. Patrick Soutter3, Phillip Gishen1 and Nandita M. deSouza1

1 Department of Imaging, Hammersmith Hospital, DuCane Rd., London W12 0HS, England.
2 Department of Histopathology, Hammersmith Hospital, London W12 0HS, England.
3 Department of Gynaecology, Hammersmith Hospital, London W12 0HS, England.

Received May 5, 2004; accepted after revision July 23, 2004.

 
Address correspondence to A. Saini.


Introduction
Top
Introduction
Materials and Methods
Results and Discussion
Conclusion
References
 
Thorough pretreatment evaluation is basic to the successful management of suspected adnexal masses because the nature and timing of surgery can be optimized if the nature of the lesion can be predicted. Although sonography is indisputably the primary imaging approach [1], MRI provides additional information on the composition of soft-tissue masses using differences in MR relaxation properties seen in various types of tissue [24]. This information is invaluable in determining the character of soft-tissue masses. In the pelvis, MRI has been shown to have a 91–93% overall accuracy for differentiating benign from malignant adnexal tumors [5] particularly when gadolinium-enhanced techniques are used [6]. This pictorial essay reviews the key differentiating MRI features of adnexal masses by correlating the MR appearances with the findings at histopathology.


Materials and Methods
Top
Introduction
Materials and Methods
Results and Discussion
Conclusion
References
 
MR images of 45 consecutive patients aged 28–87 years (mean ± SD, 53.6 ± 16.0 years) with adnexal masses diagnosed at clinical examination or on sonography were reviewed retrospectively. MRI was performed on a 1.5-T scanner (Intera, Philips Medical Systems) using a four-channel synergy pelvic phased-array coil. A reduction in bowel peristalsis was achieved by intramuscular injection of 20 mg of hyoscine-N-butyl bromide. Coronal and axial T1-weighted spin-echo images (TR/TE, 700/20), axial and sagittal T2-weighted fast spin-echo images (TR/effective TE, 4,500/80), and coronal STIR images (TR/TE, 3,000/30; inversion time, 165 msec) were obtained with a 256 x 256 matrix, a 5- to 6-mm slice thickness, and a 30-cm field of view.


Results and Discussion
Top
Introduction
Materials and Methods
Results and Discussion
Conclusion
References
 
Solid lesions of a benign nature were characterized by fat, hemorrhage, or fibrous components. Mature teratomas (dermoid cysts, n = 4) possessed high fat content and contained derivatives of all three germ layers, with a predominance of ectodermal components (Figs. 1A, 1B, and 1C). Fat was identified on STIR images, although use of fat-saturated chemical shift techniques is preferable to avoid confusion of fat with hemorrhagic lesions having the same T1 relaxation time as fat. T2-weighted images are invaluable for differentiation in these cases. Hemorrhage was a predominant feature of endometriomas (n = 7, Figs. 2A, 2B, 2C, and 2D) but also was seen in some malignant tumors. Ovarian fibromas and cystadenofibromas share a similar distinctive tissue component of dense fibrous tissue [7]. They showed a distinctive short T2 relaxation (Figs. 3A and 3B), typically shorter than that of skeletal muscle. Fibrothecomas are also of stromal origin with fibrous component similar to fibromas. They had prominent myxoid degenerative change and a less dense stroma, which increased the T2 relaxation time (Figs. 4A and 4B). Low signal intensity on T2-weighted images also was seen within the fibrotic component of cystadenofibromas (n = 3). Benign Brenner tumors (n = 2) are histologically identifiable by islands of transitional epithelium in a dense fibrotic stroma and so predictably had MR signal characteristics similar to those of a fibroma (Figs. 5A and 5B).



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Fig. 1A. —40-year-old woman with mature teratoma. Coronal T1-weighted spin-echo image (TR/TE, 700/20) shows bilateral partly solid, partly cystic, multiloculated masses (arrows) with high signal intensity.

 


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Fig. 1B. —40-year-old woman with mature teratoma. Coronal STIR image (3,000/30; inversion time, 165 msec) shows nulling of high signal intensity, indicating fat content (arrows). Dermoid cysts contain derivatives of all three germ layers with predominance of ectodermal components.

 


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Fig. 1C. —40-year-old woman with mature teratoma. Photomicrograph of histopathologic section obtained through mass shows locules of fat, together with skin and appendages (hair follicles indicated by arrowheads). (H and E, x80)

 


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Fig. 2A. —46-year-old woman with endometrioma. Coronal T1-weighted spin-echo image (TR/TE, 700/20) shows high signal intensity (arrow) in adnexal mass from methemoglobin.

 


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Fig. 2B. —46-year-old woman with endometrioma. Coronal STIR image (3,000/30; inversion time, 165 msec) shows nulling of signal intensity in region (arrow). T1 relaxation time of methemoglobin may be similar to that of fat.

 


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Fig. 2C. —46-year-old woman with endometrioma. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows well-defined adnexal mass with diffuse low signal intensity on periphery (arrow), corresponding to hemorrhage.

 


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Fig. 2D. —46-year-old woman with endometrioma. Photomicrograph of histopathologic section obtained through mass shows inner lining of endometrial-type epithelium is lost and replaced by hemosiderin-laden macrophages and hemorrhage (arrowhead). (H and E, x60)

 


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Fig. 3A. —55-year-old woman with fibroma. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows well-circumscribed solid mass (arrow) that is heterogeneous and low in signal intensity but contains extremely low-signal-intensity components posteriorly.

 


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Fig. 3B. —55-year-old woman with fibroma. Photomicrograph of histopathologic section shows that low signal intensity represents fibroblastic cellular mass in connective tissue stroma. (H and E, x400)

 


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Fig. 4A. —51-year-old woman with fibrothecoma. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows large, well-defined solid mass with homogeneously intermediate signal intensity (solid arrow). Degenerative cystic change is seen centrally with high-signal-intensity component (open arrow). Loculated ascites (arrowhead) is present and is common feature of these tumors.

 


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Fig. 4B. —51-year-old woman with fibrothecoma. Photomicrograph of histologic section shows that mass was composed of elongated fibroblasts with fairly abundant and vacuolated cytoplasm in loose stroma (compare with Fig. 3B). (H and E, x400)

 


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Fig. 5A. —68-year-old woman with Brenner tumor and cystadenoma. Coronal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows bilateral adnexal masses (arrows). Inferiorly, left-sided mass has solid component (arrowhead) with very low signal intensity (relative to that of skeletal muscle). Right-sided mass is cystic and multilocular. It represents associated serous cystadenomas (compare with Fig. 6A).

 


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Fig. 5B. —68-year-old woman with Brenner tumor and cystadenoma. Photomicrograph of histologic section obtained through solid component shows benign transitional epithelial clusters (Walthard's cell nests, arrowheads) scattered in dense fibrous stroma, characteristic of Brenner tumor. (H and E, x100)

 



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Fig. 6A. —52-year-old woman with serous cystadenoma. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows thin-walled unilocular cyst with small nodule projecting from its anterior wall (arrow). Patient had previously undergone hysterectomy.

 

Benign cystic lesions comprise serous or mucinous cystadenomas (n = 5). Cystadenomas are the most common benign epithelial tumors and were recognized as thin-walled unilocular or multilocular cysts (Figs. 6A and 6B). Borderline tumors (n = 4) lacked stromal invasion and were mainly cystic with solid components and papillary projections (Figs. 7A, 7B, and 7C). However, they often lacked secondary features of malignancy such as ascites or omental cake.



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Fig. 6B. —52-year-old woman with serous cystadenoma. Photomicrograph of histologic section reveals thin-walled simple cyst lined by bland serous epithelium, confirming diagnosis. (H and E, x600)

 


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Fig. 7A. —27-year-old woman with borderline serous tumor. Axial T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows well-defined multicystic left adnexal mass (arrows) with numerous nodular papillary projections (arrowhead) that extend into cystic component.

 


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Fig. 7B. —27-year-old woman with borderline serous tumor. Sagittal T2-weighted image shows multicystic mass (solid arrows) with nodules (arrowhead) in relation to residual normal-appearing left ovary (open arrow).

 


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Fig. 7C. —27-year-old woman with borderline serous tumor. Photomicrograph of histologic section shows that projections are composed of fibrovascular cores lined by stratified columnar cells, with no evidence of atypia. (H and E, x400)

 

Malignant cystic lesions consist of epithelial ovarian tumors (n = 8) and were distinguished by their morphology (Figs. 8A and 8B) rather than by their tissue signal intensity. The number and size of papillary projections and presence of ascites have been described as important predictors of malignancy [4]. Endometrioid adenocarcinomas (n = 1) are cystic primary ovarian tumors that resembled neoplasia found in the endometrium (Figs. 9A and 9B). They are often associated with endometrial carcinoma of the uterus or endometriosis.



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Fig. 8A. —63-year-old woman with serous cystadenocarcinoma. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows cystic mass (solid arrows) with large papilliform solid component projecting into it posteriorly (arrowhead) and breaching capsule (open arrow).

 


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Fig. 8B. —63-year-old woman with serous cystadenocarcinoma. Photomicrograph of histologic section shows irregular papillary projections that extend into cystic component (arrowhead). (H and E, x40)

 


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Fig. 9A. —43-year-old woman with endometrioid adenocarcinoma. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows large adnexal mass (solid arrows), predominantly cystic with solid papillary components (arrowhead) within it. Uterus is bulky with mass in endometrial cavity (open arrow).

 


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Fig. 9B. —43-year-old woman with endometrioid adenocarcinoma. Photomicrograph of histologic section shows malignant endometrial epithelium (arrowheads) near surface of ovary with areas of necrosis. Uterine lesion was entirely intramucosal and represented synchronous tumor. (H and E, x100)

 

Malignant solid ovarian masses are less common than cystic tumors. Granulosa cell tumors (n = 2) are slow-growing, predominantly solid masses with variable amounts of cystic change [8] and intratumoral hemorrhage (Figs. 10A and 10B). An immature teratoma (n = 1) did not contain any significant cystic component (Figs. 11A and 11B). Clear cell carcinomas (n = 2) also were recognized as predominantly solid masses with more modest cystic elements (Figs. 12A, 12B, and 12C).



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Fig. 10A. —79-year-old woman with granulosa cell tumor. Sagittal T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows well-defined solid mass (arrows) composed of large areas of homogeneous, intermediate-signal-intensity tissue with scattered high-signal-intensity cystic elements (arrowhead) seen centrally.

 


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Fig. 10B. —79-year-old woman with granulosa cell tumor. Photomicrograph of histopathologic section shows solid nest of granulosa cells with typical convoluted and grooved nuclei. (H and E, x400)

 


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Fig. 11A. —38-year-old woman with immature malignant teratoma. Axial T2-weighted fast spin-echo image (TR/effective TE, 4,500/80) shows well-defined solid mass in left adnexa (arrows) comprising areas of mixed signal intensity. Normal ovary (arrowhead) is seen on right. Cx = cervix.

 


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Fig. 11B. —38-year-old woman with immature malignant teratoma. Photomicrograph of histologic section shows that tumor consists of moderately differentiated cells that are not terminally differentiated, indicating immature teratoma. Tumor infiltration through muscular layer of adjacent colon (arrowheads) is seen. (H and E, x400)

 


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Fig. 12A. —50-year-old woman with clear cell carcinoma. Coronal T1-weighted spin-echo image (TR/TE, 700/20) shows encapsulated adnexal mass with mucinous cystic component (arrow) that has high signal intensity and large solid element (arrowhead).

 


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Fig. 12B. —50-year-old woman with clear cell carcinoma. Coronal STIR image (3,000/30; inversion time, 165 msec) corresponding to A shows partial nulling of mucinous cystic component of mass (arrow). Peripheral rim of very low signal intensity (arrowhead) around solid component represents hemorrhage.

 


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Fig. 12C. —50-year-old woman with clear cell carcinoma. Photomicrograph of histologic section reveals characteristic clear cells (vesicular nuclei and prominent nucleoli with typical hobnailing). (H and E, x600)

 

Inflammatory masses (n = 3) also presented as complex adnexal cysts. In these cases, the clinical history and examination were key in making the diagnosis. A schematic for characterizing ovarian masses on the basis of MRI features is given in Figure 13.



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Fig. 13. —Schematic for characterizing ovarian masses is based on MRI features.

 


Conclusion
Top
Introduction
Materials and Methods
Results and Discussion
Conclusion
References
 
The ability to manipulate tissue contrast with MRI makes this technique an invaluable tool in the assessment of complex adnexal masses, enabling characterization of such masses and identification of features associated with less common diseases.


References
Top
Introduction
Materials and Methods
Results and Discussion
Conclusion
References
 

  1. Funt SA, Hann LE. Detection and characterization of adnexal masses. Radiol Clin North Am2002; 40:591 -608[Medline]
  2. Outwater EK, Dunton CJ. Imaging of the ovary and adnexa: clinical issues and applications of MR imaging. Radiology1995; 194:1 -18[Abstract/Free Full Text]
  3. Huber S, Medl M, Baumann L, Czembirek H. Value of ultrasound and magnetic resonance imaging in the preoperative evaluation of suspected ovarian masses. Anticancer Res2002; 22:2501 -2507[Medline]
  4. Jeong YY, Outwater EK, Kang HK. Imaging evaluation of ovarian masses. RadioGraphics2000; 20:1445 -1470[Abstract/Free Full Text]
  5. Sohaib SAA, Sahdev A, Van Trappen P, Jacobs IJ, Reznek RH. Characterization of adnexal lesions on MR imaging. AJR2003; 180:1297 -1304[Abstract/Free Full Text]
  6. Hricak H, Chen M, Coakley FV, et al. Complex adnexal masses: detection and characterization with MR imaging—multivariate analysis. Radiology2000; 214:39 -46[Abstract/Free Full Text]
  7. Outwater EK, Siegelman ES, Talerman A, Dunton C. Ovarian fibromas and cystadenofibromas: MRI features of the fibrous component. J Magn Reson Imaging 1997;7:465 -471[Medline]
  8. Morikawa K, Hatabu H, Togashi K, Kataoka ML, Mori T, Konishi J. Granulosa cell tumor of the ovary: MR findings. J Comput Assist Tomogr 1997;21:1001 -1004[Medline]

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