A Practical Approach to the Ultrasound Characterization of Adnexal
Transcription
A Practical Approach to the Ultrasound Characterization of Adnexal
CORE CURRICULUM IN SONOGRAPHY CME ARTICLE A Practical Approach to the Ultrasound Characterization of Adnexal Masses Douglas L. Brown, MD Abstract: Because pelvic ultrasound is commonly used to evaluate adnexal masses, it is important to understand the most useful sonographic features for predicting benign and malignant masses. Determining whether an adnexal mass is of ovarian or extraovarian origin is key in arriving at the most likely diagnosis. Most adnexal masses are benign, and each of the most common benign ovarian lesions has a typical sonographic appearance. Additionally, most malignant ovarian neoplasms have a solid component with detectable flow by Doppler ultrasound, allowing one to strongly suggest the diagnosis. We will review an approach to the ultrasound diagnosis of adnexal masses that progresses through a series of 4 questions to help lead one to the most likely diagnosis. Key Words: ovary, adnexa, neoplasm, cancer, Doppler (Ultrasound Quarterly 2007;23:87Y105) LEARNING OBJECTIVES 1. Describe the most predictive ultrasound features of the 5 most common benign ovarian masses. 2. Identify the sonographic features most predictive of ovarian malignancies. 3. Describe a systematic ultrasound approach to determine the most likely diagnosis for an adnexal mass. P elvic ultrasound is frequently the first imaging modality used when abnormalities are suspected of the ovaries or adnexa. It is incumbent on sonographers and physicians who perform and interpret pelvic ultrasound to understand the most useful sonographic features. It is of little use to our patients or referring physicians to give an exceedingly long differential diagnosis or report a mass as just a Bcomplex cyst^ without further description or characterization. Most adnexal masses are benign, and we now have enough accumulated ultrasound knowledge to confidently recognize most benign adnexal masses. Many adnexal masses have such a typical ultrasound appearance that a reasonably confident Received for publication December 29, 2006; accepted March 16, 2007. Professor of Radiology, Mayo Clinic, Department of Radiology, Rochester, MN. Dr Brown has disclosed that he has no financial interests in or relationships with any commercial companies pertaining to this educational activity. Lippincott Continuing Medical Education Institute, Inc. has identified and resolved all faculty conflicts of interest regarding this educational activity. Reprints: Douglas L. Brown, MD, Mayo Clinic, Department of Radiology, 200 First St, SW, Rochester, MN 55905 (e-mail: [email protected]). Copyright * 2007 by Lippincott Williams & Wilkins Ultrasound Quarterly diagnosis can be made by ultrasound.1 Using the power of this knowledge will serve our patients well by allowing for more conservative management when appropriate and decreasing patient and physician anxiety. Most malignant masses can also be recognized by ultrasound. There will be occasional problematic cases, but we can serve our patients best by knowing the common and predictive sonographic appearances of both benign and malignant adnexal masses. In this article, we will review a practical approach to the ultrasound diagnosis of adnexal masses. This approach progresses through a series of 4 general questions in an attempt to arrive at the most likely diagnosis. Those 4 questions are the following: 1. Is the adnexal mass extraovarian in origin? 2. If the mass is ovarian in origin, is it one of the BBig 5^? 3. Does the clinical history help? 4. Is it a complex cystic mass, or is it a solid mass? There admittedly will be cases that remain problematic after this or any approach, but they are infrequent. Occasionally, other imaging modalities such as computed tomography (CT), positron emission tomography, or magnetic resonance (MR) scanning can be helpful. Magnetic resonance, in particular, has a role in the characterization of so-called indeterminate adnexal masses.2 However, it is my view that the designation of a mass as indeterminate is variable and inconsistent, with the potential to designate too many masses as indeterminate if the interpreting physician is not actively involved in evaluating these masses. I believe that the number of seemingly Bindeterminate^ adnexal masses will be minimal if one is aware of the sonographic features to be discussed here. IS THE ADNEXAL MASS EXTRAOVARIAN IN ORIGIN? Although most adnexal masses arise from the ovary, diagnostic errors will be made if one assumes an adnexal mass is of ovarian origin. It is important to try to make the distinction of ovarian versus extraovarian origin during the real-time scan. Seeing ovarian tissue with follicles extending around the mass will help confirm an ovarian origin in the premenopausal patient. Ovarian origin may be more difficult to determine with large masses or in the postmenopausal patient with a small ovary without follicles. Recognition of an ipsilateral ovary separate from the mass allows for ready determination of an extraovarian origin. The most problematic cases occur when no ovarian tissue is seen around the mass or separate from the mass. In such cases, the origin may & Volume 23, Number 2, June 2007 Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 87 Ultrasound Quarterly Brown not be clear, and one may need to consider both ovarian and extraovarian causes. Occasionally, in these cases, the mass has features typical of, for instance, a dermoid or a hydrosalpinx that will allow one to suggest the likely diagnosis even without knowing the origin of the mass for certain. Although one cannot always distinguish ovarian from extraovarian origin, there are a few things that can be done during the scan to increase the likelihood of making this distinction. During transvaginal scanning, gentle pressure with the transvaginal transducer and/or with a hand on the patient’s abdomen may be useful. When some ovarian tissue is seen immediately adjacent to an adnexal mass, such pressure may help to separate the two in cases of an extraovarian mass. Additionally, one should look with a transabdominal transducer, even if the bladder is empty, as this might reveal a separate ovary superiorly or laterally in the pelvis. Another feature that may be useful is the vascular supply of the lesion. This is most likely to be helpful with pedunculated fibroids. If one can show vessels bridging between the uterus and the solid adnexal mass, then a pedunculated fibroid is likely.3,4 Most extraovarian adnexal masses are benign.5 Several extraovarian masses have characteristic features that allow one to make an accurate diagnosis. Table 1 lists some extraovarian masses that one may encounter. It is not an allinclusive list, and the designations of common versus uncommon and typical imaging appearance may be open to debate. We will consider several of the more common extraovarian masses listed in Table 1. & Volume 23, Number 2, June 2007 FIGURE 1. Paraovarian cyst. Image from a transvaginal ultrasound of the right adnexa reveals a simple cyst (between arrows). The cyst is adjacent to, but separate from, the right ovary (O). Paraovarian Cyst It is not unusual to encounter a paraovarian or paratubal cyst during a pelvic sonogram.6 The term paraovarian cyst will be used here, realizing that one cannot typically determine exactly where they arise by ultrasound, and the distinction does not seem to be clinically important. These typically appear as simple cysts by ultrasound (Fig. 1) and are indistinguishable from ovarian cysts if one does not recognize the extraovarian location.7,8 Occasionally, paraovarian cysts have internal echoes due to hemorrhage.9 Paraovarian Cystadenoma TABLE 1. Causes of Extraovarian Masses in the Female Pelvis Predominately cystic masses Common Uncommon Predominately solid masses Common Uncommon Variable sonographic appearance Common Uncommon 88 Paraovarian cyst Hydrosalpinx Peritoneal inclusion cyst Paraovarian cystadenoma Tarlov cyst Bladder diverticulum Lymphocele Abscess Varices Paraovarian cystadenomas or cystadenofibromas (Fig. 2) are uncommon but should be considered when an extraovarian cyst contains a mural nodule or septation.6,10,11 Malignancy is rare in such lesions, although they are often removed surgically. This seems to be the same lesion histologically that occurs with increased frequency in the epididymis of men with von Hippel-Lindau syndrome.12,13 Pedunculated fibroid Neural neoplasms Lymphadenopathy Rudimentary horn of unicornuate uterus Tubal pregnancy Fallopian tube neoplasm Gastrointestinal tract lesions Neoplasms Appendiceal mucocele Appendicitis Meckel diverticulum Distended iliopsoas bursa FIGURE 2. Paraovarian cystadenoma. Image from a transvaginal ultrasound shows cystic mass with a nodular solid component (arrow). The ipsilateral ovary (not shown) was separate from the cystic mass. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 Ultrasound Characterization of Adnexal Masses Hydrosalpinx A hydrosalpinx should be considered when one encounters an elongated cystic mass with a tubular shape14 that is not a vessel (Fig. 3A). Incomplete septations (Fig. 3B), which, in a hydrosalpinx, likely represent the wall of the distended tube as it folds on itself, were initially reported to be a reliable indicator of a hydrosalpinx.15,16 A recent study, however, found that an incomplete septation, although more common in hydrosalpinges than in other lesions, was not a reliable discriminator.17 That study found the waist sign, defined as indentations along opposite sides of the cystic mass, to be the most discriminating ultrasound feature of a hydrosalpinx (Fig. 3C).17 One may also encounter small nodular-appearing areas along the wall of a hydrosalpinx (Fig. 3B), referred to as Bbeads-on-a-string^ which are probably due to abnormal endosalpingeal folds.16 One should be careful not to mistake small tortuous veins with slow flow for a hydrosalpinx. The flow may be so slow that it is not detectable by Doppler techniques, and thus, one might assume that it is a hydrosalpinx. Increasing the gray scale gain slightly and looking for movement of lowlevel echoes in the lumen will help one recognize such veins with slow flow. Fallopian tube carcinoma is rare tumor18 and is an uncommon exception to the rule that extraovarian adnexal masses are benign lesions. It should be considered if one encounters a solid mass or papillary projections within an extraovarian tubular cystic mass (Fig. 4).19,20 It may rarely be difficult to distinguish such a solid component that is worrisome for a tubal carcinoma from the projections described as Bbeads-on-a-string^ in a chronic hydrosalpinx. In my experience, the nodular areas in a chronic hydrosalpinx seem to be smaller and multiple, whereas the solid component in a fallopian tube neoplasm is larger and often is solitary. Peritoneal Inclusion Cyst The peritoneal inclusion cyst (PIC) has also been referred to by other terms, including peritoneal pseudocyst FIGURE 3. Hydrosalpinx. A, Image from a transvaginal ultrasound reveals a tubular cystic mass with a partial septation (arrow). A normal ovary (not shown) was seen separate from the mass. B, Image from a transvaginal ultrasound in a different patient. This hydrosalpinx contains a partial septation (arrowheads) and multiple small nodular areas (arrows) along the wall because of thickened endosalpingeal folds. If one did not recognize that this lesion was extraovarian in location, it could be mistaken for an ovarian carcinoma. C, Image from a transvaginal ultrasound in another patient with hydrosalpinx reveals a tubular cystic mass with the ‘‘waist sign’’ (arrows). The calipers mark the adjacent ovary. However, it seems uncommon in women, and the strength of its association with von Hippel-Lindau syndrome in women is not clear. FIGURE 4. Transvaginal ultrasound with color Doppler ultrasound image (shown in grayscale) of the left adnexa shows a solitary, relatively large, solid mass (M) within a dilated fallopian tube (between arrows). Flow was detected within the solid component. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 89 Ultrasound Quarterly Brown & Volume 23, Number 2, June 2007 Tarlov Cyst Tarlov cysts, also referred to as perineural or root sleeve cysts, are uncommon, but it is important to recognize them because they can be mistaken for gynecologic pathology and treated inappropriately. Patients could potentially undergo unnecessary or harmful surgery if these are not recognized. Most Tarlov cysts are asymptomatic and discovered incidentally.26 Rarely, surgery may be performed if they are felt to be the cause of pain.26 Tarlov cysts may be unilateral or bilateral. Small Tarlov cysts are not typically seen by ultrasound, and it is usually the larger cysts that are seen sonographically. Tarlov cysts almost always have internal echoes,27Y29 although it is not clear what these echoes represent (Fig. 6). The cysts tend to appear as slightly elongated or beaded cystic masses posteriorly. This might present some confusion with a hydrosalpinx, but Tarlov cysts do not tend to be as elongated and tubular as a hydrosalpinx, although this admittedly is a subjective evaluation that may be difficult. One would also probably not expect to see an incomplete septation or Bwaist sign^ in a Tarlov cyst. Computed tomography or MR can be used to confirm the diagnosis of a Tarlov cyst and readily shows their origin from sacral neural foramina. FIGURE 5. Peritoneal inclusion cyst. A, Transverse image from a transabdominal ultrasound of the pelvis shows cystic mass with septations (arrows). B, Image from a transvaginal ultrasound in the same patient shows normal ovary (between arrows) at the edge of the cystic mass (labeled C), with the mass extending around the ovary. U indicates uterus. and inflammatory cyst of the peritoneum. It is thought to be caused by peritoneal adhesions that trap fluid produced by a functioning ovary. Most patients have a history of prior pelvic surgery, endometriosis, or pelvic inflammatory disease (PID) that results in pelvic adhesions. Several articles have described the ultrasound appearance of PICs.21Y25 The ovary typically appears to be inside the PIC by sonography, often at the periphery of the cyst. Most PICs have septations. In 1 study, gentle pressure with the transvaginal transducers showed movement of the septations in 48% of PICs.25 Such mobility of septations has been suggested as more common in PICs than in neoplasms25; however, to my knowledge, this has not been confirmed in other studies. The fluid is typically anechoic, but there can be internal echoes. Peritoneal inclusion cysts may have bizarre shapes25 and sometimes conform to the shape of the surrounding structures, a feature which may be more evident on CT or MR scanning. Thus, when one encounters a septated cystic pelvic mass in a patient with a history of pelvic surgery, endometriosis, or PID, a careful search should be made for a normal ovary within or at the periphery of the cystic mass (Fig. 5). 90 FIGURE 6. Tarlov cysts. A, Transverse transabdominal ultrasound image reveals 3 adjacent cystic masses posteriorly on the left. B, Transvaginal ultrasound image of one of the posterior left adnexal masses in the same patient reveals internal echoes within the cystic mass (between arrows). The left ovary (not shown) was seen separate from all 3 lesions. B indicates bladder; U, uterus. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 IF THE MASS IS OVARIAN IN ORIGIN, IS IT ONE OF THE BIG 5? Once one has confirmed an ovarian origin of the mass, the most common lesions need to be considered. Most ovarian masses encountered in clinical imaging practices are benign. Simple cysts, hemorrhagic cysts, corpora lutea, endometriomas, and dermoids are likely to be the most frequent ovarian masses that one will encounter. I refer to these as the BBig 5^ because they are so common and usually have a typical ultrasound appearance that allows one to make a confident diagnosis. A small percentage of these lesions will not have the classic appearance. In such cases, knowledge of the more frequent atypical findings will allow one to favor a particular diagnosis, although with a lesser degree of confidence than when the lesion has the classic appearance. Simple Cyst An ovarian follicle typically reaches a mean diameter of 20 to 24 mm (range, 17Y27 mm) at the time of ovulation.30,31 Although follicles technically are simple cysts, I believe it is better to refer to them as Bfollicles^ rather than Bcysts^ because the latter has potential to be misinterpreted as something that may be abnormal or need follow-up.32 Thus, I would generally consider a simple cyst less than about 25 mm in mean diameter to be normal in the ovary of a premenopausal woman. A simple cyst in the ovary should meet the same criteria as a simple cyst in any organ: anechoic, thin wall, and distal acoustic enhancement. As many ovarian simple cysts (Fig. 7) will resolve, the cause is not often proven. Many are probably follicular cysts. A small percentage of corpus luteal cysts are simple cysts by sonography.33 Serous cystadenoma can appear as a simple cyst and is a more likely consideration with simple cysts that are large and those in older patients. The approach to followup of simple ovarian cysts in premenopausal women is not standardized. It has been suggested that simple cysts of less than 3 cm do not require followup.34 FIGURE 7. Simple ovarian cyst. Transvaginal ultrasound images shows a simple cyst (labeled C) arising from the right ovary. Ultrasound Characterization of Adnexal Masses Simple ovarian cysts occur in 3.5% to 17% of postmenopausal women.35 On follow-up ultrasound, most such cysts either disappear or remain stable.36Y39 Only a small percentage, generally less than approximately 10%, increase in size.36Y39 In many lefts, a simple cyst that remains less than 5 cm in size is managed with follow-up ultrasound.34,40Y42 If the cyst becomes larger than 5 cm or changes appearance, surgery is usually warranted.34,41 Of those cysts treated surgically, the majority are serous cystadenomas.42 This brings up the question of the frequency of malignancy in a simple ovarian cyst. We generally assume that this is uncommon, although there are occasional reports of malignancy in simple ovarian cysts.43Y45 These were typically older studies using transabdominal transducers, or the sonographic methods were not always clear. In a more recent study of a large number of cases with well-defined methods and use of transvaginal scanning, the frequency of malignancy in simple ovarian cysts was 0.7% in premenopausal women and 1.6% in postmenopausal women.40 Interestingly, all malignancies occurred in cysts of larger than 7.5 cm in mean diameter. Pathologically, there were usually small mural nodules that were not seen sonographically. Therefore, for cysts that are well seen with transvaginal scanning (and also with transabdominal scanning when needed for larger cysts), the likelihood of malignancy in simple cysts of less than 7.5 cm is virtually nil. The authors suggested that the 5-cm threshold for conservative versus surgical management remains valid.40 Thus, we should recognize that, for larger cysts, there is a slight chance that small nodular areas along the cyst wall can be missed, probably because of the larger surface area to be evaluated. Sonographers and sonologists should carefully scrutinize the entire inner cyst wall in these lesions. Hemorrhagic Cyst Hemorrhagic cysts occur commonly in the ovaries of premenopausal women. The patient may present for medical care because of acute pain. A recent study found 2 particular sonographic features to be reliable.46 Hemorrhagic cysts often have internal echoes with a pattern of fine interdigitating lines46 that have been variously described as Breticular,^ Bfishnet,^ or Blacelike^ and are believed to be caused by fibrin strands that result when clot hemolyzes.34,46 This reticular or fishnet pattern (Fig. 8A) due to fibrin strands was found to have a sensitivity of 90%, specificity of 98%, and positive likelihood ratio (LR) of 40 for hemorrhagic cysts.46 Fibrin strands have the potential to be confused with septations.46 However, fibrin strands tend to be very thin, rarely extend all the way across a cyst, and arc within the cyst, as opposed to true septations that have more substance and are hence thicker and extend to opposite walls of the cyst in a linear or slight curvilinear fashion. The other reliable ultrasound feature which is retracting clot (solid echoes with a concave margin) was found to have an even higher LR (967) and specificity (100%), but its sensitivity was only 30% (Fig. 8B). The combination of fibrin strands, no septations, and smooth walls was found to have an LR of 200, with sensitivity of 90% and specificity of 100%.46 It has been suggested that follow-up ultrasound of classic hemorrhagic * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 91 Ultrasound Quarterly Brown & Volume 23, Number 2, June 2007 cysts is probably not necessary unless the patient remains symptomatic.46,47 Occasionally, hemorrhagic cysts have other appearances. In these instances, one is not likely to confidently make the diagnosis on a single sonogram but would at least consider the possibility and suggest a follow-up sonogram. Most hemorrhagic cysts will resolve within 6 to 8 weeks.34,47 Infrequently, the clot may have convex outer margins and simulate a solid area of a neoplasm (Fig. 8B). Absence of flow in the seemingly solid area by Doppler ultrasound is reassuring, but follow-up ultrasound is generally needed. A minority of hemorrhagic cysts will have heterogeneous internal echoes and seem to be solid (Fig. 8C); this likely is caused by acute or subacute clot.47 Doppler ultrasound can be useful to consider this possibility and not send the patient directly to surgery for a solid ovarian neoplasm before obtaining a follow-up ultrasound. Fluid-fluid levels occasionally occur in hemorrhagic cysts.47 In my experience, the more echogenic fluid is located dependently in hemorrhagic cysts. Corpus Luteum FIGURE 8. Hemorrhagic ovarian cysts. A, Transvaginal ultrasound image shows a complex cystic mass (between arrows) with a reticular or fishnet pattern of internal echoes. This is the classic appearance of a hemorrhagic ovarian cyst. B, Transvaginal ultrasound image shows 2 hemorrhagic cysts in the left ovary. Seemingly solid area in one of the cysts has a concave margin (arrow), which is suggestive of clot. The other seemingly solid area (arrowhead) did not have concave margins. This can also occur with clot but makes it harder to distinguish from true solid tissue of a neoplasm. Both cystic lesions resolved on follow-up ultrasound 1 month later. C, Transvaginal ultrasound image of a hemorrhagic cyst (between arrows) in the acute to subacute stage. As opposed to lesion in part A, the echoes in this cyst are more heterogeneous and more echogenic, potentially leading one to suspect a solid mass. Color Doppler ultrasound (not shown) showed no flow within the lesion, and it resolved on follow-up ultrasound. 92 It is important to recognize the corpus luteum (CL) as a normal finding in premenopausal women and not mistake it for something more sinister. One expects to see the CL in the secretory phase of the menstrual cycle and in the first trimester of pregnancy. It may also be seen in the subsequent follicular phase.48 The appearance of the CL has been described in a few studies using transvaginal sonography.33,48,49 Unfortunately, the ability to discriminate the CL from true abnormalities by sonography has not, to my knowledge, been investigated. Different schemes to describe its appearance have also been used. Although these technically are cysts, usually complex cysts, it has been suggested that we refer to them as a CL, rather than a corpus luteal cyst, unless they are larger than approximately 4 to 5 cm.32 The CL is typically less than approximately 3 cm in diameter.49 The CL often appears as a small cystic lesion with a crenulated wall and low-level internal echoes (Fig. 9A),34,50 although it may have a variable appearance. In a study of the CL during the normal menstrual cycle, the majority had a central cystic cavity.48 The minority had no such cystic cavity48 and appeared as a hypoechoic to isoechoic area in the ovary. Central cystic areas became less frequent with increasing time from ovulation. The wall was described as thickened and irregular but was not a specific feature that was evaluated.48 In another study of the CL in early pregnancy, 34% of patients had a CL that was hypoechoic compared with the ovary (Fig. 9B), 27% had a thick-walled cyst with anechoic center, 23% had a cyst with internal echoes, and 15% had a simple cyst.33 The wall is usually hypoechoic or isoechoic compared with adjacent ovarian parenchyma.51 The isoechoic or slightly hypoechoic lesions may be overlooked.33 In my opinion, small lesions that have one of these typical appearances in a premenopausal patient should be considered as the normal CL. I admit, however, that the discriminatory ability of such features has not been proven, and there will be some cases where one is not * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 Ultrasound Characterization of Adnexal Masses reasonably certain that the lesion is a CL, and follow-up ultrasound may be appropriate. The CL is typically a very vascular structure, and one should not be surprised to see abundant flow peripherally49 by color or power Doppler ultrasound (Fig. 9C). Corpora lutea may also incidentally be identified on CT, typically as lesions of less than 3 cm with thick, crenulated, enhancing walls.52 Endometrioma Ultrasound is not reliable for identifying the small deposits of endometriosis but is useful for identifying endometriomas.53 Although the deposits of endometrial tissue may occur in many locations and are common on peritoneal surfaces, endometriomas usually occur in the FIGURE 9. Corpus luteum. A, Transvaginal ultrasound image shows a CL (between the calipers), appearing as a complex cystic mass with a crenulated wall and internal echoes in a central cystic cavity. Small amount of free fluid (labelled FF) is also present. B, Transvaginal ultrasound image in a different patient shows a hypoechoic appearance to the CL (marked by calipers). This can result when the internal echoes are similar in echogenicity to the wall of the lesion. Corpora lutea with this appearance can be overlooked because they are often similar in echogenicity to the adjacent ovary. C, Transvaginal ultrasound image with color Doppler ultrasound from the same patient as in part B shows abundant flow around the periphery of the CL (arrows). FF indicates free fluid. FIGURE 14. Color plates for images 14A, 14B and 14C. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 93 Ultrasound Quarterly Brown ovary.54 Endometriomas (Fig. 10A) typically have homogeneous low- to medium-level internal echoes.55Y58 The appearance of hemorrhagic cysts and endometriomas overlaps58Y60 in a small percentage of cases, but endometriomas tend to have more homogeneous internal echoes as opposed to the more heterogeneous and reticular pattern in hemorrhagic cysts. This homogeneous appearance has sometimes been referred to as a Bground glass^ appearance.1 & Volume 23, Number 2, June 2007 Although diffuse homogeneous internal echoes are very common and quite typical of endometriomas, other lesions will occasionally have low-level internal echoes.58,61 Acoustic streaming, a technique using Doppler ultrasound to show movement or lack of movement of the internal echoes, has been suggested as a potential method to help distinguish endometriomas from other lesions with internal echoes.62 Initial results seem promising because most endometriomas are reported not to have acoustic streaming, but further experience is needed. Septations with resulting multilocularity are common, occurring in 45% of endometriomas in 1 study.58 Hyperechoic wall foci were observed in 35% of endometriomas (Fig. 10B) and were found to be a useful feature for diagnosing endometriomas.58 To my knowledge, no other studies have evaluated this feature of endometriomas. Wall nodularity (Fig. 10C) occurs in approximately 20% of endometriomas58 and is problematic because this feature typically raises concern for a neoplasm. Color Doppler ultrasound or MR may be helpful in such instances,58 but their value in this situation has not been proven. It has been speculated that these solid areas are caused by clot or fibrin.1 If so, one would expect there to be no detectable flow by color Doppler ultrasound. I have anecdotally seen a few cases where the nodular area was caused by endometrial tissue, in which case, flow may be detectable by Doppler ultrasound and then confused for a neoplasm. At least 1 case of an endometrioma with a nodular area containing flow has been reported.63 Infrequently, an endometrioma may have a solid appearance.1,34,61 In my experience, this solid appearance (Fig. 10B) tends to occur with the more chronic ovarian endometriomas. It is not always clear whether they are really solid lesions or just appear that way because of older blood products and/or fibrosis. Additionally, extraovarian deposits of endometriosis may infrequently be large enough to be identified by ultrasound, and such deposits tend to be solid.54,64 When one detects a cystic mass with diffuse, homogeneous, low-level internal echoes and no nodular areas, an endometrioma is very likely. Multilocularity and/or hyperechoic wall foci may further increase the likelihood of an endometrioma. FIGURE 10. Endometrioma. A, Transvaginal ultrasound image of a typical endometrioma with homogeneous low- to medium-level internal echoes. This lesion has 2 locules (labeled 1 and 2). Endometriomas may be unilocular or multilocular. B, Transvaginal ultrasound image of 3 adjacent endometriomas in the right ovary in a different patient. Endometriomas 1 and 2 are essentially isoechoic to the ovary and could be mistaken for solid lesions; both of these have small echogenic foci (arrows) along part of their periphery. Endometrioma 3 is not homogeneous, likely because of more recent internal hemorrhage. C, Transvaginal ultrasound image of an endometrioma in another patient. Homogeneous internal echoes (labeled E) are present, but there is also a solid appearing area (arrow) that is slightly hyperechoic compared with the internal echoes. Such solid-appearing areas are probably caused by a clot or a focal area of endometrial tissue. 94 * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 Mature Cystic Teratoma Mature cystic teratomas, often referred to as dermoids, are the most common ovarian neoplasm.34,65 Most dermoids have one of several typical sonographic findings, allowing a confident diagnosis by ultrasound. Most dermoids can be accurately characterized by ultrasound.66 For the rare case where one is not sure if it has typical sonographic features of a dermoid, CT or MR can be performed. Either imaging modality should allow easy recognition of macroscopic fat and confirm the diagnosis of a dermoid. My personal view is that MR is generally the better alternative imaging modality. If there is no macroscopic fat, CT typically provides little in the way of further clues to the diagnosis. Endometriomas, however, are one of the more common false positive diagnoses for dermoid, and MR will often allow a confident diagnosis of an endometrioma. It is also important to note that most dermoids do not have detectable flow within the lesion by color Doppler ultrasound. As dermoids are prone to torsion, it is important to assess for flow in some adjacent normal ovary rather than in the dermoid itself when torsion of a dermoid is being considered. A hyperechoic area (Fig. 11A), particularly one that attenuates sound (Fig. 11B), is a common sonographic finding in dermoids. This feature is believed to be caused by a mixture of hair and sebum.1,67 The terminology used to describe this hyperechoic area is variable and includes dermoid plug,68 Rokitansky protuberance,68 densely echogenic tubercle,69,70 echogenic nodule or mass,67,71 hyperechoic solid component,72 and regional bright echoes.66 The Btip of the iceberg^ sign (Fig. 11B) refers to such marked shadowing from the hyperechoic area that the deeper part of the mass is not seen.73 The hyperechoic solid area is typically of high echogenicity, although not as intensely echogenic as calcification. This high degree of echogenicity is usually obvious after one has seen typical examples, but there may be occasional cases where one is not sure if the area is echogenic enough to be typical of a dermoid. Magnetic resonance should be considered in such cases. Occasionally, the entire mass may be hyperechoic (Fig. 11C).67 The presence of distal acoustic shadowing, often originating in the hyperechoic area, further increases the likelihood of a dermoid.66,71 The shadowing may have the appearance of a progressive fading of the sound beam, probably because of a mixture of hair and sebum, or can appear as a sharp well-defined shadow caused by calcification.67 Shadowing in dermoids is most frequently due to attenuation of sound by the mixture of hair and sebum, rather than due to calcification.73 Another typical feature of dermoids is the Bdermoid mesh^ appearance that consists of hyperechoic lines and dots (Fig. 11D).74,75 It is believed to be caused by hair within nonfatty fluid.1,74,75 This is a useful sign, although fibrin strands in a hemorrhagic cyst or air in an abscess occasionally may cause confusion. Fortunately, it seems that, in most dermoids with this mesh appearance, there is also another typical finding such as hyperechoic areas, shadowing, or a fatfluid level. A fluid-fluid level (Fig. 11E) has also been described in dermoids76,77 but is an infrequent finding.66,71 As an isolated finding, it may not have much diagnostic value, but there are Ultrasound Characterization of Adnexal Masses often other sonographic features also present that are typical of a dermoid.66,77 One might expect that the fatty fluid would be more echogenic and would be the nondependent layer of fluid. In fact, when there is a fluid-fluid level in a dermoid, most often, the nondependent fluid is hypoechoic, and the dependent fluid is hyperechoic.77 Although the nondependent fluid is always the fatty fluid by CT or MR, the echogenicity of the fatty fluid by ultrasound is variable.77 Pure sebum, which is liquid at body temperature, has been reported to be anechoic or hypoechoic.67 This may be the explanation in dermoids where the nondependent fluid is less echogenic. Other lesions such as hemorrhagic cysts, endometriomas, and ovarian neoplasms will occasionally have fluid-fluid levels, but in all such cases, the dependent fluid is more echogenic.77 Thus, as an isolated finding, a fluid-fluid level where the dependent fluid is more echogenic than the nondependent fluid is not very predictive of any particular pathology. However, the nondependent fluid will be more echogenic in a minority of dermoids with a fluid-fluid level (30% in 1 study77). Thus, when the fluid-fluid level has this appearance with a more echogenic nondependent layer, a dermoid seems very likely because this pattern was not seen in any other lesions.77 If one recognizes a floating nodule at the interface between the 2 fluid layers, this also seems predictive of a dermoid.77 There is one other appearance that seems very predictive of a dermoid, but it is uncommon. Different terminology has been used to describe this appearance, but it consists of multiple floating globules, spherules, or balls within a cystic mass (Figs. 11F, 11G).78Y82 Because this is an uncommon appearance, its predictive value has not been carefully evaluated, although it has been suggested to be pathognomonic of a dermoid.78 Such lesions are typically large cystic masses (usually greater than approximately 10 cm and often 20 to 30 cm), and the globules tend to be fairly uniform in size. They rarely have any of the other typical sonographic features of a dermoid as discussed above. The floating balls are often described as hyperechoic or markedly echogenic, although, to my review, the echogenicity is not always as hyperechoic as typical of most dermoids. The globules have been reported to contain hair, sebaceous debris, keratin, and fibrin.78Y81,83Y87 Occasionally, MR shows no evidence of macroscopic fat in the floating globules.81 Most ovarian teratomas are benign. Malignant transformation is reported to occur in 1% to 3% of ovarian teratomas,88Y91 but this is based mostly on pathological series. Even these low rates seem high in my experience, and I suspect the frequency is considerably less in clinical practice because small dermoids are sometimes followed clinically. Lower malignancy rates of 0.17% to 0.3% for ovarian teratomas have also been reported.92,93 The malignancy rate may be higher in postmenopausal women and was reported at 15% in 1 study.94 There is little information in the literature describing sonographic features that one might use to predict malignancy of ovarian teratomas. Branching isoechoic solid components have been suggested as a feature of malignancy.95 The most common histology with malignant transformation of ovarian teratomas is squamous cell carcinoma.93 Serum squamous cell carcinoma antigen levels * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 95 Brown 96 Ultrasound Quarterly & Volume 23, Number 2, June 2007 * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 have been suggested as a possible parameter to diagnose malignancy in ovarian teratomas, but it may be of limited value.96 With MR imaging, solid components with transmural extension or contrast enhancement suggest malignancy.97,98 Malignant teratomas are more likely than benign teratomas to have detectable blood flow within solid areas by color Doppler ultrasound.96 However, the use of this feature in clinical practice is not clear because malignant teratomas are uncommon, and 20% of benign teratomas have some area of detectable flow by color Doppler ultrasound.96 It was not clear, however, where the flow was detected in these 20% of patients with benign teratomas. Another report found that none of the benign teratomas had detectable flow in the Bcenter^ of tumor.99 Additionally, struma ovarii, although also uncommon, may have detectable blood flow. Struma ovarii, a benign monodermal form of teratoma composed mostly of thyroid tissue, has a different pathological appearance from most mature cystic teratomas.100 Its ultrasound appearance is also variable,100 and struma ovarii is one of the more difficult lesions to reliably characterize by ultrasound.101 DOES THE CLINICAL HISTORY HELP? If the above questions do not lead to a likely diagnosis, there are a few instances when the clinical history can be quite useful. This question is mainly to consider the possibility of TOAs because their sonographic appearance is quite variable. Generally, one will already be aware of this possibility based on the clinical presentation before doing the sonogram. History is also helpful for theca lutein cysts, although they usually have a characteristic ultrasound appearance. Tubo-ovarian Abscess Tubo-ovarian abscess (TOA) results when a lower genital tract infection ascends and results in salpingitis and then ovarian inflammation to the degree that there is breakdown of normal appearance of the adnexal structures.16 Ultrasound Characterization of Adnexal Masses The term tubo-ovarian complex has been suggested when there are inflammatory changes, but the ovary remains recognizable by ultrasound.16 The term tubo-ovarian abscess is suggested when there is further progression of inflammatory change with resulting breakdown of the adnexal structures such that the ovary is not separately recognized.16 The distinction is important because an abscess may require drainage, whereas a complex may not.34 Despite ultrasound being a common imaging method in patients with a suspected TOA, there is surprisingly little in the literature evaluating ultrasound’s overall usefulness in this setting.102 There are several studies describing ultrasound for patients with PID but little actual description of the sonographic findings for a TOA.16,103Y106 The ultrasound appearance of TOAs is variable1 (Fig. 12), but they usually have a cystic component1,106,107 and may have septations, thick walls, internal echoes, and/or seemingly solid areas. The appearance overlaps with other lesions including neoplasms34 and hemorrhagic cysts. A minority of TOAs have a tubular component suggestive of a pyosalpinx.106 The presence of an associated pyosalpinx, which appears like a hydrosalpinx but with internal echoes in the fluid is a suggestive sonographic finding.104,106,107 Unless there is a pyosalpinx component, there does not seem to be a predictive ultrasound appearance for a TOA. Given this variable ultrasound appearance, the clinical findings with signs and symptoms of PID are helpful,106 if not necessary, to make the diagnosis of TOA. Theca Lutein Cysts Theca lutein cysts typically appear as bilateral cystic masses with multiple septations.107 They are believed to be caused by an ovarian response to high levels of human chorionic gonadotropin. One would likely suspect theca lutein cysts by their typical appearance (Fig. 13), although having an appropriate clinical history is helpful in making a more confident diagnosis. Theca lutein cysts are associated with gestational trophoblastic disease but can occasionally be seen with a multiple pregnancy, fetal hydrops, or a normal FIGURE 11. Mature cystic teratoma. A, Transvaginal ultrasound image of a complex cystic mass reveals that a portion of the mass consists of a hyperechoic solid component (between the arrows), typical of a mature cystic teratoma (also known as a dermoid). In this case, there is little, if any, distal shadowing from the hyperechoic component. B, Transvaginal ultrasound image shows a complex cystic mass (outlined by the calipers) in a different patient. A portion of it consists of a hyperechoic nodule (arrowheads), from which distal acoustic shadowing (between the arrows) originates. The acoustic shadowing obscures the deeper portion of the hyperechoic nodule, which has been referred to as the ‘‘tip of the iceberg’’ sign. C, Transvaginal ultrasound image with color Doppler ultrasound (shown in grayscale) in another patient reveals a uniformly hyperechoic mass (arrows). Note that there is no flow detected within the mass. Although dermoids are prone to torsion, one should not expect to detect flow within most dermoids by color Doppler ultrasound. Therefore, when considering ovarian torsion in a patient with a dermoid, one needs to look for flow in a portion of normal ovary adjacent to the dermoid. D, Transvaginal ultrasound image in another patient reveals a complex cystic mass with the dermoid mesh appearance, which consists of hyperechoic lines and dots (some of which are indicated by arrowheads). This mass also contains a hyperechoic solid area (arrow). E, Transvaginal ultrasound image in a different patient reveals a fluid-fluid level (arrows), with the hyperechoic fluid being nondependent. F, Transabdominal ultrasound image of another patient demonstrates multiple solid nodules (asterisks) nondependently within a large cystic mass. This has been referred to as floating fat balls and other names. These nodules are not as hyperechoic as in some of the more typical dermoids as illustrated above, but the ‘‘floating’’ nature of the nodules is suggestive of a dermoid. G, Sagittal T2-weighted image with fat saturation of the same patient as in part F again demonstrates the multiple ‘‘floating’’ nodules. Patient was scanned in the supine position. In this case, there was no fat evident on T1-weighted sequences with fat saturation. Figure 11F and 11G courtesy of Dr. Peter Hanson and Dr. Karl Stein, Wabasha, MN. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 97 Ultrasound Quarterly Brown FIGURE 12. Tubo-ovarian abscess. A, Transvaginal ultrasound image shows a complex cystic mass (outlined by calipers). At least 2 locules are seen, each with internal echoes. This ultrasound appearance may suggest hemorrhagic cysts or endometriomas, but the clinical setting was suggestive of PID. B, Transvaginal ultrasound image in another patient shows a complex cystic mass. This mass contains a mixed cystic and solid area that may raise concern for a neoplasm. The clinical setting in this case, however, was suggestive of PID. & Volume 23, Number 2, June 2007 appearance of the more common ovarian neoplasms will usually allow one to favor a particular diagnosis. Ovarian neoplasms are often grouped into 4 general histological categories: surface epithelial neoplasms, germ cell neoplasms, sex cordYstromal neoplasms, and metastatic neoplasms. Although there are malignant forms in the other categories, most ovarian cancers are epithelial neoplasms. Epithelial neoplasms include serous, mucinous, endometrioid, and clear-cell types. Serous and mucinous neoplasms have benign and malignant forms, whereas endometrioid and clear cell neoplasms are nearly always malignant. 109 Endometrioid and clear cell carcinomas are the most common carcinomas to arise in endometriomas.54 Transitional cell tumors, sometimes referred to as Brenner tumors, are infrequent epithelial tumors and are usually benign.109 Additionally, borderline tumors have been described for all surface epithelial cell types but are, by far, most common in the serous and mucinous cell types.110 Borderline tumors, sometimes called tumors of low malignant potential or atypical proliferating tumors, have less stromal invasion than frankly malignant tumors. Borderline tumors are malignant, but they carry a better prognosis than frankly malignant tumors.110 Of the germ cell group of neoplasms, mature cystic teratomas are by far the most common89 and have been discussed above. Less frequent neoplasms in this group include dysgerminoma, yolk sac tumor, and embryonal carcinoma. These other germ cell tumors are usually solid but can have areas of cystic change.111 Fibroma is the most common neoplasm in the sex cordYstromal group; other neoplasms in this group include thecomas, granulosa cell tumors, and Sertoli-Leydig cell tumors.112 Metastatic neoplasms constitute the fourth group and will be further discussed below. We will review sonographic features that suggest an ovarian neoplasm, particularly malignant neoplasms, and then apply those to the different histological groups of ovarian neoplasms. The presence of a solid component (Figs. 14AYC), which is not the typical hyperechoic component of a dermoid, singleton pregnancy (known as hyperreactio luteinalis).108 This appearance is also the same as seen with ovarian hyperstimulation syndrome during assisted reproductive techniques.108 After the high human chorionic gonadotropin stimulus for their formation is removed, it may take several weeks for the cysts to resolve.107 IS IT A COMPLEX CYSTIC MASS, OR IS IT A SOLID MASS? If the series of questions have not lead to a likely diagnosis by this point, ovarian neoplasm (other than the mature cystic teratoma as discussed above) is becoming more likely. One will not always be able to make a specific diagnosis at this point, but knowledge of the most frequent 98 FIGURE 13. Theca lutein cysts. Transabdominal ultrasound image reveals a large cystic ovarian mass (outlined by calipers) with multiple locules, typical of theca lutein cysts. The other ovary (not shown) had a similar appearance. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 Ultrasound Characterization of Adnexal Masses FIGURE 14. Epithelial ovarian neoplasms. A, Transabdominal ultrasound image with color Doppler ultrasound shows a large complex cystic pelvic mass containing a solid nodular area (between the arrows) that has flow by color Doppler ultrasound. This was a serous adenocarcinoma of the right ovary. B, Transvaginal ultrasound image in another patient demonstrates a complex cystic mass. One might consider an endometrioma, in this case, due to the internal echoes; however, there were 2 solid areas that had flow by color Doppler ultrasoundVone of which is shown in this image (arrow). This was a serous borderline tumor of the right ovary. C, Transvaginal ultrasound image with color Doppler ultrasound from another patient reveals a complex cystic mass with a small nodular solid area (arrow) along the wall. Color Doppler ultrasound shows only a small focus of flow at the base of the nodule. This was a papillary cystadenofibroma of the right ovary. D, Transvaginal ultrasound image in a different patient reveals a complex cystic adnexal mass with a septation (arrowhead) and solid nodular areas (arrows). This was a borderline serous tumor of the left ovary. E, Transvaginal ultrasound image from a different patient shows a complex cystic mass (between arrows) with multiple septations. No solid areas were seen. This was a mucinous cystadenoma. F, Transvaginal ultrasound image shows a large adnexal mass (between the arrows) that is partly cystic but has a large heterogeneous solid component and a few septations. This was a clear cell adenocarcinoma. See color plates for images 14A, 14B and 14C on page 93. is the most useful feature for identifying ovarian malignancy.72,113 Other terminology has been used to refer to these solid areas, including papillary vegetation, papillary projections, and nodularity. Ovarian cancer is often unilocular and may not therefore have any septations.72 If septations are present, thicker septations (typically considered as greater than 2 to 3 mm) are more typical of malignancy (Fig. 14B). Ascites, other than the normal trace amount that is frequently seen in premenopausal women, is also predictive of ovarian cancer but tends to occur with later stage disease.72 Although ovarian malignancy is associated with larger masses,5 the sonographic morphology of a mass is a more useful predictor of malignancy than its size.72,114 Upon reviewing our data from a previously published study of 28 ovarian malignan- cies,72 12 malignant masses (43%) were less than 5 cm in mean diameter, 8 (29%) were less than 4 cm in mean diameter, and 6 (21%) were less than 3 cm in mean diameter. In one of the well-recognized studies of ovarian cancer screening with sonography, the authors reported volume rather than diameters.115 If one assumes a spherical shape (which I realize is not likely but would probably skew the calculation to only a small degree) and calculates the diameter corresponding with those volumes, 8 (47%) of 17 ovarian malignancies in that study would have been less than 4 cm in diameter. Although there is a trend for malignant ovarian masses to be larger than benign ovarian masses, small ovarian lesions can still be malignant. Thus, one should not disregard a mass just because it is small, and should still carefully evaluate its morphology. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 99 Ultrasound Quarterly Brown For large masses that seem to be simple cysts, careful scrutiny of all the inner wall is important because tiny solid nodules can be missed.40 Doppler evaluation initially received lots of interest, but the pulsed Doppler ultrasound parameters of resistive index, pulsatility index, peak systolic velocity, and timeaveraged maximum velocity do not allow any significant & Volume 23, Number 2, June 2007 improvement over morphological assessment. Thus, the use of pulsed Doppler analysis is limited.72,116 Optimal characterization occurs with the combination of gray scale ultrasound for morphological assessment and color Doppler imaging.117,118 Assessing for solid areas by gray scale ultrasound and by color or power Doppler imaging to detect flow within any solid area (Figs. 14A, 14C) are the 2 most useful features for identifying malignancy.72,116,118Y120 Although one can often predict an ovarian neoplasm by this combined approach, it may be difficult to distinguish a benign from malignant neoplasm (Fig. 14D) because benign neoplasms may also have detectable flow in solid areas.119 The risk of malignancy increases with larger and more irregular solid components.1 Although probably not widely done, Doppler ultrasound assessment of vessel size and orientation may be helpful, with erratic course and changing caliber of vessels more typical of malignant masses.121 Published studies have evaluated various methods for categorizing the ultrasound features of ovarian masses, including gray scale ultrasound alone and in combination with Doppler imaging. Scoring systems, mathematical models of probability, and artificial neural networks have been developed. Although these work fairly well, they are somewhat cumbersome to use. Results of these and other studies, however, have provided us with the most important features to assess. Knowing those features and evaluating them in a subjective method have proven to be useful. Subjective assessment by an experienced examiner, using proven sonographic features, is a highly reliable method to differentiate benign from malignant adnexal masses and performs better than at least some of the mathematical models.122,123 I believe this is the easiest method to incorporate into most clinical practices, and it has been shown to be reliable. Thus, it behooves the ultrasound practitioner to be cognizant of these more reliable ultrasound features. For complex cystic lesions that are more cystic than solid, epithelial neoplasm should generally be the first consideration. Although there are occasional exceptions, serous and mucinous neoplasms tend to be predominately cystic with a smaller solid component (Figs. 14AYE). Endometrioid and clear cell carcinomas (Fig. 14F) tend to have a larger solid component. Mucinous cystadenomas tend FIGURE 15. Ovarian fibroma. A, Transvaginal ultrasound image demonstrates a 7-cm solid mass (between the arrows) in the right adnexa. It was difficult to know if this was of ovarian origin because the right ovary was not seen. B, Another transvaginal ultrasound image from the same patient shows a tiny echogenic focus (arrow) at the periphery of the solid mass. Such echogenic foci in the ovaries are not usually thought to be of clinical significance but, as in this case, can sometimes be helpful in identifying the ovary.35 C, Transvaginal ultrasound image in a different patient reveals an area of marked acoustic shadowing originating within the right adnexa. One might not recognize the solid mass (labeled M) accounting for the shadowing and could discount this as bowel gas. However, this was a consistent well-defined focal area of shadowing during the scan. Notice that the shadowing does not originate from a bright interface, as might be expected with shadowing from calcification, a dermoid, or bowel gas. 100 * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 Ultrasound Characterization of Adnexal Masses TABLE 2. Four Questions to Consider When Evaluating an Adnexal Mass FIGURE 16. Virilizing stromal neoplasm. A 39-year-old patient presented with virilizing symptoms and elevated testosterone levels. Transvaginal ultrasound image demonstrates a subtle, small, isoechoic mass (labeled M) in the left ovary. Such a mass could be easily overlooked or attributed to a corpus luteum. Surgical resection revealed an 11 6 4-mm Leydig cell tumor of the left ovary. to appear as cystic masses with multiple septations and no solid areas (Fig. 14E), whereas serous cystadenomas tend to be unilocular or bilocular cystic masses with no solid areas.1,118,124,125 However, the appearance of these benign lesions overlaps with each other and occasionally with malignancy, making it difficult to render a confident diagnosis of serous or mucinous cystadenomas in some cases.1 When a tumor is predominately solid, one should consider the sex cordYstromal group of tumors. Although some of the tumors in this group, particularly if larger, can have a cystic component; many are solid. The most common FIGURE 17. Metastasis to the ovary. Transvaginal ultrasound image reveals a solid mass (labeled M) replacing the left ovary. The right ovary (not shown) appeared similar. This was caused by metastasis from breast cancer. 1. Is the adnexal mass extraovarian in origin? If so, consider more common lesions such as paraovarian cyst hydrosalpinx Peritoneal inclusion cyst 2. If the mass is ovarian in origin, is it one of the BBig 5^? Evaluate for suggestive features of a simple cyst hemorrhagic cyst corpus luteum endometrioma mature cystic teratoma (dermoid) 3. Does the clinical history help? Mainly to consider tubo-ovarian abscess or theca lutein cyst 4. Is it a complex cystic mass or is it a solid mass? Evaluate for solid areas not typical of a dermoid and use color or power Doppler ultrasound to assess for flow in the solid areas. These findings are useful for predicting neoplasms. If more cystic than solid, consider epithelial neoplasms first. If mostly or entirely solid, consider sex cordYstromal neoplasms first if unilateral and metastases if bilateral. neoplasm in this group is the fibroma. It usually appears as a solid mass that can be homogeneous or heterogeneous and may attenuate sound (Fig. 15).126Y130 Occasionally, it can have marked attenuation of sound (Fig. 15C).126,128,130 Fibromas are almost always benign tumors. There is a spectrum with thecomas, and both histological types can occur in the same tumor. The thecoma component can secrete estrogens. Fibromas have a similar appearance to uterine leiomyomas. Thus, when one identifies a solid adnexal mass but does not identify an ipsilateral ovary, the primary differential diagnosis is ovarian fibroma versus pedunculated leiomyoma. Granulosa cell tumors are low-grade malignancies and are the most common ovarian tumor to secrete estrogen.127 In my experience and that of others,127 granulosa cell tumors are commonly solid, although a complex cystic appearance with solid areas or septations has been described.131 Estrogen secretion from granulosa cell tumors can cause endometrial thickening and abnormal vaginal bleeding.131 Sertoli-Leydig cell, and other related, tumors are also part of the sex cordYstromal group. It is the most common ovarian tumor to secrete androgens and can cause virilizing symptoms.127,132 Most virilizing ovarian neoplasms are small solid tumors that can be subtle (Fig. 16).127,132 When a virilizing ovarian neoplasm is being considered, one should be suspicious of any subtle abnormality in the ovary and at least obtain a follow-up ultrasound. Occasionally, these tumors can have a cystic component.127 When faced with a seemingly solid lesion, one should also consider mimics of solid ovarian masses: pedunculated uterine leiomyoma, chronic endometrioma, and subacute hemorrhagic cyst. Brenner tumor is an uncommon benign epithelial tumor that also tends to be solid and may coexist with other ovarian neoplasms.133,134 * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 101 Ultrasound Quarterly Brown Metastatic neoplasms have a variable appearance. When considering all types of ovarian neoplasms, there are few features useful in distinguishing primary versus secondary ovarian malignancy.135 Multilocularity is more common, however, in primary, versus secondary, neoplasms.135 The most common primary sources of metastasis to the ovary include breast, colon, gastric, and appendiceal carcinomas.136Y140 When considering these more frequent primary sources, the presence of bilateral solid masses (Fig. 17) is suggestive of metastases.34,141Y143 Metastasis to the ovaries from breast cancer usually occurs in the setting of advanced stage disease.144,145 It is more variable whether metastasis from other primary tumors have a known primary carcinoma before the metastasis is discovered.135 19. SUMMARY 20. Knowing the most useful sonographic features for common benign tumors, which are different from the sonographic features of most malignant tumors, will allow one to make a confident diagnosis or generate a short list of differential diagnoses in most cases. Progressing through these series of 4 questions is 1 approach to the sonographic diagnosis of adnexal masses that I have found to work well. Table 2 briefly summarizes this approach. There will be occasional problematic cases, whether because of limited scan quality, confusing sonographic appearance, or rare lesions that are not easily characterized, but this approach works well for most adnexal masses. REFERENCES 1. Valentin L. Use of morphology to characterize and manage common adnexal masses. Best Pract Res Clin Obstet Gynaecol. 2004;18:71Y89. 2. Adusumilli S, Hussain HK, Caoili EM, et al. MRI of sonographically indeterminate adnexal masses. AJR Am J Roentgenol. 2006; 187:732Y740. 3. Kim SH, Sim JS, Seong CK. Interface vessels on color/power Doppler US and MRI: a clue to differentiate subserosal uterine myomas from extrauterine tumors. J Comput Assist Tomogr. 2001;25:36Y42. 4. Madan R. The bridging vascular sign. Radiology. 2006;238:371Y372. 5. Lee SI. Radiological reasoning: imaging characterization of bilateral adnexal masses. AJR Am J Roentgenol. 2006;187(suppl 3):S460YS466. 6. Savelli L, Ghi T, De Iaco P, et al. Paraovarian/paratubal cysts: comparison of transvaginal sonographic and pathological findings to establish diagnostic criteria. Ultrasound Obstet Gynecol. 2006;28:330Y334. 7. Barloon TJ, Brown BP, Abu-Yousef MM, et al. Paraovarian and paratubal cysts: preoperative diagnosis using transabdominal and transvaginal sonography. J Clin Ultrasound. 1996;24:117Y122. 8. Kim JS, Woo SK, Suh SJ, et al. Sonographic diagnosis of paraovarian cysts: value of detecting a separate ipsilateral ovary. AJR Am J Roentgenol. 1995;164:1441Y1444. 9. Alpern MB, Sandler MA, Madrazo BL. Sonographic features of parovarian cysts and their complications. AJR Am J Roentgenol. 1984;143:157Y160. 10. Korbin CD, Brown DL, Welch WR. Paraovarian cystadenomas and cystadenofibromas: sonographic characteristics in 14 cases. Radiology. 1998;208:459Y462. 11. Ghossain MA, Braidy CG, Kanso HN, et al. Extraovarian cystadenomas: ultrasound and MR findings in 7 cases. J Comput Assist Tomogr. 2005;29:74Y79. 12. Korn WT, Schatzki SC, DiSciullo AJ, et al. Papillary cystadenoma of the broad ligament in von Hippel-Lindau disease. Am J Obstet Gynecol. 1990;163:596Y598. 13. Funk KC, Heiken JP. Papillary cystadenoma of the broad ligament in a 102 14. 15. 16. 17. 18. 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. 38. & Volume 23, Number 2, June 2007 patient with von Hippel-Lindau disease. AJR Am J Roentgenol. 1989;153:527Y528. Tessler FN, Perrella RR, Fleischer AC, et al. Endovaginal sonographic diagnosis of dilated fallopian tubes. AJR Am J Roentgenol. 1989;153:523Y525. Guerriero S, Ajossa S, Lai MP, et al. Transvaginal ultrasonography associated with colour Doppler energy in the diagnosis of hydrosalpinx. Hum Reprod. 2000;15:1568Y1572. Timor-Tritsch IE, Lerner JP, Monteagudo A, et al. Transvaginal sonographic markers of tubal inflammatory disease. Ultrasound Obstet Gynecol. 1998;12:56Y66. Patel MD, Acord DL, Young SW. Likelihood ratio of sonographic findings in discriminating hydrosalpinx from other adnexal masses. AJR Am J Roentgenol. 2006;186:1033Y1038. Pectasides D, Pectasides E, Economopoulos T. Fallopian tube carcinoma: a review. Oncologist. 2006;11:902Y912. Kurjak A, Kupesic S, Jacobs I. Preoperative diagnosis of the primary fallopian tube carcinoma by three-dimensional static and power Doppler sonography. Ultrasound Obstet Gynecol. 2000;15:246Y251. Patlas M, Rosen B, Chapman W, et al. Sonographic diagnosis of primary malignant tumors of the fallopian tube. Ultrasound Q. 2004;20:59Y65. Guerriero S, Ajossa S, Mais V, et al. Role of transvaginal sonography in the diagnosis of peritoneal inclusion cysts. J Ultrasound Med. 2004;23:1193Y1200. Hoffer FA, Kozakewich H, Colodny A, et al. Peritoneal inclusion cysts: ovarian fluid in peritoneal adhesions. Radiology. 1988;169: 189Y191. Kim JS, Lee HJ, Woo SK, et al. Peritoneal inclusion cysts and their relationship to the ovaries: evaluation with sonography. Radiology. 1997;204:481Y484. Kurachi H, Murakami T, Nakamura H, et al. Imaging of peritoneal pseudocysts: value of MR imaging compared with sonography and CT. AJR Am J Roentgenol. 1993;161:589Y591. Savelli L, de Iaco P, Ghi T, et al. Transvaginal sonographic appearance of peritoneal pseudocysts. Ultrasound Obstet Gynecol. 2004;23: 284Y288. Slipman CW, Bhat AL, Bhagia SM, et al. Abdominal pain secondary to a sacral perineural cyst. Spine J. 2003;3:317Y320. Forsnes EV, Segna RA. Dural ectasia presenting as an adnexal mass. Obstet Gynecol. 1996;88:712Y713. Raza S, Klapholz H, Benacerraf BR. Tarlov cysts: a cause of complex bilateral adnexal masses on pelvic sonography. J Ultrasound Med. 1994;13:803Y805. McClure MJ, Atri M, Haider MA, et al. Perineural cysts presenting as complex cystic adnexal masses on transvaginal sonography. AJR Am J Roentgenol. 2001;177:1313Y1318. Bakos O, Lundkvist O, Wide L, et al. Ultrasonographical and hormonal description of the normal ovulatory menstrual cycle. Acta Obstet Gynecol Scand. 1994;73:790Y796. Ritchie WGM. Sonographic evaluation of normal and induced ovulation. Radiology. 1986;161:1Y10. Timor-Tritsch IE, Goldstein SR. The complexity of a Bcomplex mass^ and the simplicity of a Bsimple cyst^. J Ultrasound Med. 2005;24: 255Y258. Durfee SM, Frates MC. Sonographic spectrum of the corpus luteum in early pregnancy: gray-scale, color, and pulsed Doppler appearance. J Clin Ultrasound. 1999;27:55Y59. Dill-Macky M, Atri M. Ovarian sonography. In: Callen P, ed. Ultrasonography in Obstetrics and Gynecology. 4th ed. Philadelphia: WB Saunders Company; 2000:857Y896. Parsons A. Whither the simple cyst in postmenopausal women? (opinion). Ultrasound Obstet Gynecol. 2002;20:112Y116. Conway C, Zalud I, Dilena M, et al. Simple cyst in the postmenopausal patient: detection and management. J Ultrasound Med. 1998;17: 369Y372. Goldstein SR, Subramanyam B, Snyder JR, et al. The postmenopausal cystic adnexal mass: the potential role of ultrasound in conservative management. Obstet Gynecol. 1989;73:8Y10. Kroon E, Andolf E. Diagnosis and follow-up of simple ovarian cysts detected by ultrasound in postmenopausal women. Obstet Gynecol. 1995;85:211Y214. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 39. Levine D, Gosink BB, Wolf SI, et al. Simple adnexal cysts: the natural history in postmenopausal women. Radiology. 1992;184: 653Y659. 40. Ekerhovd E, Wienerroith H, Staudach A, et al. Preoperative assessment of unilocular adnexal cysts by transvaginal ultrasonography: a comparison between ultrasonographic morphologic imaging and histopathologic diagnosis. Am J Obstet Gynecol. 2001;184:48Y54. 41. Oyelese Y, Kueck AS, Barter JF, et al. Asymptomatic postmenopausal simple ovarian cyst. Obstet Gynecol Surv. 2002;57:803Y809. 42. Bailey CL, Ueland FR, Land GL, et al. The malignant potential of small cystic ovarian tumors in women over 50 years of age. Gynecol Oncol. 1998;69:3Y7. 43. Hall DA, McCarthy KA. The significance of the postmenopausal simple adnexal cyst. J Ultrasound Med. 1986;5:503Y505. 44. Luxman D, Bergman A, Sagi J, et al. The postmenopausal adnexal mass: correlation between ultrasonic and pathologic findings. Obstet Gynecol. 1991;77:726Y728. 45. Osmers RGW, Osmers M, von Maydell B, et al. Preoperative evaluation of ovarian tumors in the premenopause by transvaginosonography. Am J Obstet Gynecol. 1996;175:428Y434. 46. Patel MD, Feldstein VA, Filly RA. The likelihood ratio of sonographic findings for the diagnosis of hemorrhagic ovarian cysts. J Ultrasound Med. 2005;24:607Y614. quiz 615. 47. Jain KA. Sonographic spectrum of hemorrhagic ovarian cysts. J Ultrasound Med. 2002;21:879Y886. 48. Baerwald AR, Adams GP, Pierson RA. Form and function of the corpus luteum during the human menstrual cycle. Ultrasound Obstet Gynecol. 2005;25:498Y507. 49. Bourne TH, Hagstrom H, Hahlin M, et al. Ultrasound studies of vascular and morphological changes in the human corpus luteum during the menstrual cycle. Fertil Steril. 1996;65:753Y758. 50. Swire MN, Castro-Aragon I, Levine D. Various sonographic appearances of the hemorrhagic corpus luteum cyst. Ultrasound Q. 2004;20:45Y58. 51. Frates MC, Visweswaran A, Laing FC. Comparison of tubal ring and corpus luteum echogenicities: a useful differentiating characteristic. J Ultrasound Med. 2001;20:27Y31. 52. Borders RJ, Breiman RS, Yeh BM, et al. Computed tomography of corpus luteal cysts. J Comput Assist Tomogr. 2004;28:340Y342. 53. Woodward PJ, Sohaey R, Mezzetti TP. Endometriosis: radiologic-pathologic correlation. Radiographics. 2001;21:193Y216. 54. Clement PB. Diseases of the peritoneum. In: Kurman RJ, ed. Blaustein’s Pathology of the Female Genital Tract. New York: Springer-Verlag; 2002:729Y789. 55. Dogan MM, Ugur M, Soysal SK, et al. Transvaginal sonographic diagnosis of ovarian endometrioma. Int J Gynaecol Obstet. 1996;52:145Y149. 56. Kupfer MC, Schwimer SR, Lebovic J. Transvaginal sonographic appearance of endometriomata: spectrum and findings. J Ultrasound Medicine. 1992;11:129Y133. 57. Mais V, Guerriero S, Ajossa S, et al. The efficiency of transvaginal ultrasonography in the diagnosis of endometrioma. Fertil Steril. 1993;60:776Y780. 58. Patel MD, Feldstein VA, Chen DC, et al. Endometriomas: diagnostic performance of ultrasound. Radiology. 1999;210:739Y745. 59. Pascual MA, Tresserra F, Lopez-Martin L, et al. Role of color Doppler ultrasonography in the diagnosis of endometriotic cyst. J Ultrasound Med. 2000;19:695Y699. 60. Bhatt S, Kocakoc E, Dogra VS. Endometriosis: sonographic spectrum. Ultrasound Q. 2006;22:273Y280. 61. Kurjak A, Kupesic S. Scoring system for prediction of ovarian endometriosis based on transvaginal color and pulsed Doppler sonography. Fertil Steril. 1994;62:81Y88. 62. Clarke L, Edwards A, Pollard K. Acoustic streaming in ovarian cysts. J Ultrasound Med. 2005;24:617Y621. 63. Guerriero S, Ajossa S, Mais V, et al. The diagnosis of endometriomas using colour Doppler energy imaging. Hum Reprod. 1998;13: 1691Y1695. 64. Siegelman ES, Outwater E, Wang T, et al. Solid pelvic masses causes by endometriosis: MR imaging features. AJR Am J Roentgenol. 1994;163:357Y361. 65. Koonings PP, Campbell K, Mishell DR, et al. Relative frequency of Ultrasound Characterization of Adnexal Masses 66. 67. 68. 69. 70. 71. 72. 73. 74. 75. 76. 77. 78. 79. 80. 81. 82. 83. 84. 85. 86. 87. 88. 89. 90. primary ovarian neoplasms: a 10-year review. Obstet Gynecol. 1989;74:921Y926. Patel MD, Feldstein VA, Lipson SD, et al. Cystic teratomas of the ovary: diagnostic value of sonography. AJR Am J Roentgenol. 1998;171:1061Y1065. Sheth S, Fishman EK, Buck JL, et al. The variable sonographic appearances of ovarian teratomas: correlation with CT. AJR Am J Roentgenol. 1988;151:331Y334. Quinn SF, Erickson S, Black WC. Cystic ovarian teratomas: the sonographic appearance of the dermoid plug. Radiology. 1985;155:477Y478. Cohen L, Sabbagha R. Echo patterns of benign cystic teratomas by transvaginal ultrasound. Ultrasound Obstet Gynecol. 1993;3:120Y123. Mais V, Guerriero S, Ajossa S, et al. Transvaginal ultrasonography in the diagnosis of cystic teratoma. Obstet Gynecol. 1995;85:48Y52. Caspi B, Appelman Z, Rabinerson D, et al. Pathognomonic echo patterns of benign cystic teratomas of the ovary: classification, incidence and accuracy rate of sonographic diagnosis. Ultrasound Obstet Gynecol. 1996;7:275Y279. 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;208:103Y110. Guttman PH Jr. In search of the elusive benign cystic ovarian teratoma: application of the ultrasound Btip of the iceberg^ sign. J Clin Ultrasound. 1977;5:403Y406. Malde HM, Kedar RP, Chadha D, et al. Dermoid mesh: a sonographic sign of ovarian teratoma (letter). AJR Am J Roentgenol. 1992;159: 1349Y1350. Bronshtein M, Yoffe N, Brandes JM, et al. Hair as a sonographic marker of ovarian teratomas: improved identification using transvaginal sonography and simulation model. J Clin Ultrasound. 1991;19:351Y355. Owre A, Pedersen JF. Characteristic fat-fluid level at ultrasonography of ovarian dermoid cyst. Acta Radiol. 1991;32:317Y319. Kim HC, Kim SH, Lee HJ, et al. Fluid-fluid levels in ovarian teratomas. Abdom Imaging. 2002;27:100Y105. Kawamoto S, Sato K, Matsumoto H, et al. Multiple mobile spherules in mature cystic teratoma of the ovary. AJR Am J Roentgenol. 2001;176:1455Y1457. Rao JR, Shah Z, Patwardhan V, et al. Ovarian cystic teratoma: determined phenotypic response of keratocytes and uncommon intracystic floating balls appearance on sonography and computed tomography. J Ultrasound Med. 2002;21:687Y691. Umesaki N, Nagamatsu A, Yada C, et al. MR and ultrasound imaging of floating globules in mature ovarian cystic teratoma. Gynecol Obstet Invest. 2004;58:130Y132. Canda AE, Astarcioglu H, Obuz F, et al. Cystic ovarian teratoma with intracystic floating globules. Abdom Imaging. 2005;30:369Y371. Tongsong T, Wanapirak C, Khunamornpong S, et al. Numerous intracystic floating balls as a sonographic feature of benign cystic teratoma: report of 5 cases. J Ultrasound Med. 2006;25:1587Y1591. Otigbah C, Thompson MO, Lowe DG, et al. Mobile globules in benign cystic teratoma of the ovary. BJOG. 2000;107:135Y138. Gol M, Saygili U, Uslu T, et al. Mature cystic teratoma with intracystic fat balls in a postmenopausal woman. Eur J Obstet Gynecol Reprod Biol. 2005;119:125Y126. Muramatsu Y, Moriyama N, Takayasu K, et al. CT and MR imaging of cystic ovarian teratoma with intracystic fat balls. J Comput Assist Tomogr. 1991;15:528Y529. Jantarasaengaram S, Siricharoenthai S, Vairojanavong K. Cystic ovarian teratoma with intracystic fat balls. Ultrasound Obstet Gynecol. 2003;22:102Y103. Rathod K, Kale H, Narlawar R, et al. Unusual Bfloating balls^ appearance of an ovarian cystic teratoma: sonographic and CT findings. J Clin Ultrasound. 2001;29:41Y43. Pantoja E, Rodriguez-Ibanez I, Axtmayer RW, et al. Complications of dermoid tumors of the ovary. Obstet Gynecol. 1975;45:89Y94. Talerman A. Germ cell tumors of the ovary. In: Kurman RJ, ed. Blaustein’s pathology of the female genital tract. 5th ed. New York: Springer-Verlag; 2002:967Y1033. Caruso PA, Marsh MR, Minkowitz S, et al. An intense clinicopathologic * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 103 Ultrasound Quarterly Brown 91. 92. 93. 94. 95. 96. 97. 98. 99. 100. 101. 102. 103. 104. 105. 106. 107. 108. 109. 110. 111. 112. 113. 114. study of 305 teratomas of the ovary. Cancer. 1971;27: 343Y348. Bloomfield TH. Benign cystic teratomas of the ovary: a review of seventy-two cases. Eur J Obstet Gynecol Reprod Biol. 1987; 25:231Y237. Ayhan A, Aksu T, Develioglu O, et al. Complications and bilaterality of mature ovarian teratomas (clinicopathological evaluation of 286 cases). Aust N Z J Obstet Gynecol. 1991;31:83Y85. Comerci JT, Licciardi F, Bergh PA, et al. Mature cystic teratoma: a clinicopathologic evaluation of 517 cases and review of the literature. Obstet Gynecol. 1994;84:22Y28. Fenghua W, Zhanhong J, Chunhua Y. Analysis of 20 mature ovarian cystic teratoma cases in postmenopausal women. Chin Med J. 2001;114:137Y138. Mlikotic A, McPhaul L, Hansen GC, et al. Significance of the solid component in predicting malignancy in ovarian cystic teratomas. J Ultrasound Med. 2001;20:859Y866. Emoto M, Obama H, Horiuchi S, et al. Transvaginal color Doppler ultrasonic characterization of benign and malignant ovarian cystic teratomas and comparison with serum squamous cell carcinoma antigen. Cancer. 2000;88:2298Y2304. Rha SE, Byun JY, Jung SE, et al. Atypical CT and MRI manifestations of mature ovarian cystic teratomas. AJR Am J Roentgenol. 2004;183:743Y750. Kido A, Togashi K, Konishi I, et al. Dermoid cysts of the ovary with malignant transformation: MR appearance. AJR Am J Roentgenol. 1999;172:445Y449. Zalel Y, Seidman DS, Oren M, et al. Sonographic and clinical characteristics of struma ovarii. J Ultrasound Med. 2000;19:857Y861. Outwater E, Siegelman ES, Hunt JL. Ovarian teratomas: tumor types and imaging characteristics. Radiographics. 2001;21:475Y490. Valentin L, Ameye L, Jurkovic D, et al. Which extrauterine pelvic masses are difficult to correctly classify as benign or malignant on the basis of ultrasound findings and is there a way of making a correct diagnosis? Ultrasound Obstet Gynecol. 2006;27:438Y444. Horrow MM. Ultrasound of pelvic inflammatory disease. Ultrasound Q. 2004;20:171Y179. Cacciatore B, Leminen A, Ingman-Friberg S, et al. Transvaginal sonographic findings in ambulatory patients with suspected pelvic inflammatory disease. Obstet Gynecol. 1992;80:912Y916. Taipale P, Tarjanne H, Ylostalo P. Transvaginal sonography in suspected pelvic inflammatory disease. Ultrasound Obstet Gynecol. 1995;6:430Y434. Boardman LA, Peipert JF, Brody JM, et al. Endovaginal sonography for the diagnosis of upper genital tract infection. Obstet Gynecol. 1997;90:54Y57. Varras M, Polyzos D, Perouli E, et al. Tubo-ovarian abscesses: spectrum of sonographic findings with surgical and pathological correlations. Clin Exp Obstet Gynecol. 2003;30:117Y121. Fried AM, Kenney CM, Stigers KB, et al. Benign pelvic masses: sonographic spectrum. Radiographics. 1996;16:321Y334. al-Harbi O, al-Saleem A, al-Tayeb O, et al. Recurrent bilateral theca lutein cysts in association with normal pregnancy. Ultrasound Obstet Gynecol. 1998;11:222Y224. Seidman JD, Russell P, Kurman RJ. Surface epithelial tumors of the ovary. In: Kurman RJ, ed. Blaustein’s Pathology of the Female Genital Tract. 5th ed. New York: Springer-Verlag; 2002:791Y904. Hart WR. Borderline epithelial tumors of the ovary. Mod Pathol. 2005;18(suppl 2):S33YS50. Brammer HM, Buck JL, Hayes WS, et al. Malignant germ cell tumors of the ovary: radiologic-pathologic correlation. Radiographics. 1990;10:715Y724. Young RH, Scully RE. Sex cordYstromal, steroid cell, and other ovarian tumors with endocrine, paraendocrine, and paraneoplastic manifestations. In: Kurman RJ, ed. Blaustein’s Pathology of the Female Genital Tract. 5th ed. New York: Springer-Verlag; 2002:905Y966. Granberg S, Wikland M, Jansson I. Macroscopic characterization of ovarian tumors and the relation to the histological diagnosis: criteria to be used for ultrasound evaluation. Gynecol Oncol. 1989;35:139Y144. Tailor A, Jurkovic D, Bourne TH, et al. Sonographic prediction of malignancy in adnexal masses using multivariate logistic regression analysis. Ultrasound Obstet Gynecol. 1997;10:41Y47. 104 & Volume 23, Number 2, June 2007 115. van Nagell J, DePriest P, Reedy M, et al. The efficacy of transvaginal sonographic screening in asymptomatic women at risk for ovarian cancer. Gynecol Oncol. 2000;77:350Y356. 116. Guerriero S, Ajossa S, Risalvato A, et al. Diagnosis of adnexal malignancies by using color Doppler energy imaging as a secondary test in persistent masses. Ultrasound Obstet Gynecol. 1998;11:277Y282. 117. Kinkel K, Hricak H, Lu Y, et al. US characterization of ovarian masses: a meta-analysis. Radiology. 2000;217:803Y811. 118. Buy J, 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 Am J Roentgenol. 1996;166:385Y393. 119. Schelling M, Braun M, Kuhn W, et al. Combined transvaginal B-mode and color Doppler sonography for differential diagnosis of ovarian tumors: results of a multivariate logistic regression analysis. Gynecol Oncol. 2000;77:78Y86. 120. Cohen LS, Escobar PF, Scharm C, et al. Three-dimensional power Doppler ultrasound improves the diagnostic accuracy for ovarian cancer prediction. Gynecol Oncol. 2001;82:40Y48. 121. Kurjak A, Kupesic S, Anic T, et al. Three-dimensional ultrasound and power Doppler improve the diagnosis of ovarian lesions. Gynecol Oncol. 2000;76:28Y32. 122. Valentin L, Hagen B, Tingulstad S, et al. Comparison of pattern recognition and logistic regression models for discrimination between benign and malignant pelvic masses: a prospective cross validation. Ultrasound Obstet Gynecol. 2001;18:357Y365. 123. Timmerman D, Schwarzler P, Collins WP, et al. Subjective assessment of adnexal masses with the use of ultrasonography: an analysis of interobserver variability and experience. Ultrasound Obstet Gynecol. 1999;13:11Y16. 124. Guerriero S, Mallarini G, Ajossa S, et al. Transvaginal ultrasound and computed tomography combined with clinical parameters and CA-125 determinations in the differential diagnosis of persistent ovarian cysts in premenopausal women. Ultrasound Obstet Gynecol. 1997;9:339Y343. 125. Buy JN, Ghossain MA, Sciot C, et al. Epithelial tumors of the ovary: CT findings and correlation with US. Radiology. 1991;178:811Y818. 126. Stephenson WM, Laing FC. Sonography of ovarian fibromas. AJR Am J Roentgenol. 1985;144:1239Y1240. 127. Outwater EK, Wagner BJ, Mannion C, et al. Sex cordYstromal and steroid cell tumors of the ovary. Radiographics. 1998;18: 1523Y1546. 128. Conte M, Guariglia L, Panici PB, et al. Ovarian fibrothecoma: sonographic and histologic findings. Gynecol Obstet Invest. 1991;32:51Y54. 129. Bazot M, Ghossain MA, Buy JN, et al. Fibrothecomas of the ovary: CT and US findings. J Comput Assist Tomogr. 1993;17:754Y759. 130. Atri M, Nazarnia S, Bret PM, et al. Endovaginal sonographic appearance of benign ovarian masses. Radiographics. 1994;14:747Y760. 131. Sharony R, Aviram R, Fishman A, et al. Granulosa cell tumors of the ovary: do they have any unique ultrasonographic and color Doppler flow features? Int J Gynecol Cancer. 2001;11:229Y233. 132. Outwater EK, Marchetto B, Wagner BJ. Virilizing tumors of the ovary: imaging features. Ultrasound Obstet Gynecol. 2000;15:365Y371. 133. Athey PA, Siegel MF. Sonographic features of Brenner tumor of the ovary. J Ultrasound Med. 1987;6:367Y372. 134. Green GE, Mortele KJ, Glickman JN, et al. Brenner tumors of the ovary: sonographic and computed tomographic imaging features. J Ultrasound Med. 2006;25:1245Y1251. quiz 1252Y1254. 135. Brown DL, Zou KH, Tempany CM, et al. Primary versus secondary ovarian malignancy: imaging findings of adnexal masses in the radiology diagnostic oncology group study. Radiology. 2001;219: 213Y218. 136. Moore RG, Chung M, Granai CO, et al. Incidence of metastasis to the ovaries from nongenital tract primary tumors. Gynecol Oncol. 2004;93:87Y91. 137. Demopoulos RI, Touger L, Dubin N. Secondary ovarian carcinoma: a clinical and pathological evaluation. Int J Gynecol Pathol. 1987;6:166Y175. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. Ultrasound Quarterly & Volume 23, Number 2, June 2007 138. Holtz F, Hart WR. Krukenberg tumors of the ovary: a clinicopathologic analysis of 27 cases. Cancer. 1982;50:2438Y2447. 139. Ulbright TM, Roth LM, Stehman FB. Secondary ovarian neoplasia: a clinicopathologic study of 35 cases. Cancer. 1984;53: 1164Y1174. 140. Yakushiji M, Tazaki T, Nishimura H, et al. Krukenberg tumors of the ovary: a clinicopathologic analysis of 112 cases. Acta Obstet Gynaecol Jpn. 1987;39:479Y485. 141. Choi BI, Choo IW, Han MC, et al. Sonographic appearance of Krukenberg tumor from gastric carcinoma. Gastrointest Radiol. 1988;13:15Y18. Ultrasound Characterization of Adnexal Masses 142. Athey PA, Butters HE. Sonographic and CT appearance of Krukenberg tumors. J Clin Ultrasound. 1984;12:205Y210. 143. Salem S, Wilson SR. Gynecologic ultrasound. In: Rumack C, Wilson SR, Charboneau JW, eds. Diagnostic Ultrasound. 3rd ed. Philadelphia: Elsevier Mosby; 2005:527Y587. 144. Hann LE, Lui DM, Shi W, et al. Adnexal masses in women with breast cancer: US findings with clinical and histopathologic correlation. Radiology. 2000;216:242Y247. 145. Simpkins F, Zahurak M, Armstrong D, et al. Ovarian malignancy in breast cancer patients with an adnexal mass. Obstet Gynecol. 2005;105: 507Y513. * 2007 Lippincott Williams & Wilkins Copyright @ Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited. 105