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CHAPTER 16 The Adnexa 579

TABLE 16.1 Ovarian Neoplasms

Tumor Incidence Examples

Surface

epithelial–

stromal tumors

65%-75% Serous cystadenoma/

carcinoma

Mucinous cystadenoma/

carcinoma

Endometrioid carcinoma

Clear cell carcinoma

Transitional cell tumor

Germ cell tumors 15%-20% Teratoma

Dysgerminoma

Yolk sac tumor

Sex cord–stromal

tumors

Metastatic

tumors

5%-10% Granulosa cell tumor

Sertoli-Leydig cell tumor

Thecoma and ibroma

5%-10% Uterus

Stomach, colon, breast

Lymphoma

tumors (5%-10%). Sonographically, ovarian cancer usually

presents as an adnexal mass. Well-deined anechoic cysts are

more likely to be benign, whereas lesions with irregular walls,

thick irregular septations, mural nodules, and solid elements

with low are more likely to be malignant. 131,132 Many scoring

systems and mathematical models based on the morphologic

characteristics have been proposed for distinguishing between

benign and malignant masses. However, subjective evaluation

of the ultrasound morphologic features (pattern recognition)

by an experienced interpreting physician has been shown to be

the superior method. 133,134 Using this method, a physician should

be able to distinguish benign from malignant masses in approximately

90% of cases. 135

Color and pulsed Doppler sonography have been advocated

for distinguishing benign from malignant ovarian masses. Support

is based on the premise that malignant masses, because of internal

neovascularization, will have high diastolic low. Malignant tumor

growth depends on angiogenesis, with the development of

abnormal tumor vessels. 136 hese abnormal vessels lack smooth

muscle within their walls, which, along with arteriovenous

shunting, leads to decreased vascular resistance and thus higher

diastolic low velocity. herefore the pulsatility index (PI) and

resistive index (RI) should be lower in malignant lesions. Although

many reports have found a tendency for both PI and RI to be

lower in malignant lesions, there is too much overlap to diferentiate

reliably between benign and malignant lesions in individual

patients. 137-142 Other parameters such as vessel location have been

suggested to improve the speciicity of Doppler ultrasound

assessment of ovarian masses. 143 Malignant lesions tend to have

more central low, whereas benign lesions tend to have more

peripheral low. However, Stein et al. 138 found considerable overlap,

with 21% of malignant lesions having only peripheral low and

31% of benign lesions having central low. Guerriero et al. 144

found a higher accuracy in predicting malignancy when color

Doppler ultrasound demonstrated arterial low within the solid

portions of the mass.

Studies comparing the morphologic features on sonography

with the Doppler indings found that Doppler ultrasound showed

no more diagnostic information than morphologic assessment

alone. 133,139,140,145 Valentin 133 concluded that, in experienced hands,

morphologic assessment is the best method for discriminating

between benign and malignant masses. he main advantage of

adding Doppler ultrasound would be to increase the conidence

with which a correct diagnosis is made. Others have found that

Doppler ultrasound, when added to sonographic morphologic

assessment, improves speciicity and positive predictive value. 142,146-

148

Brown et al. 149 found that a nonhyperechoic solid component

was the most statistically signiicant predictor of malignancy.

Schelling et al. 150 also found that a solid component in an adnexal

mass with central vascularity achieved high accuracy, sensitivity,

and speciicity in predicting malignancy. A meta-analysis of 46

published studies concluded that ultrasound techniques that

combine morphologic assessment with color Doppler low imaging

is signiicantly better in characterizing ovarian masses than

morphologic assessment, color Doppler low imaging, or Doppler

indices alone. 151 Doppler ultrasound is probably not needed if

the mass has a characteristic benign morphology, because

morphologic assessment is highly accurate in this group of

lesions. 138,141 Doppler ultrasound is likely valuable in assessing

the mass that is morphologically indeterminate or suggestive of

malignancy. Doppler indings should be combined with morphologic

assessment, clinical indings, patient age, and phase of

menstrual cycle for optimal evaluation of an adnexal mass. 152

Recently, contrast-enhanced TVS (CE-TVS) has been used

to evaluate ovarian tumor neovascularity. With dynamic CE-TVS,

malignant tumor neovascularity usually demonstrates more

prolonged contrast washout compared with benign tumors. he

diference in contrast enhancement patterns between benign

and malignant ovarian masses results in potential improvement

in diferentiating benign from malignant lesions with CE-TVS

compared with conventional TVS. 153

Surface Epithelial–Stromal Tumors

In the past, epithelial-stromal tumors were generally considered

to arise from the surface epithelium that covers the ovary and

the underlying ovarian stroma. It has since been proposed that

epithelial ovarian cancer is a collection of diseases arising from

varying cells of origin. Evidence suggests that the majority of

primary ovarian cancers (in particular, high-grade serous cancers)

are derived from the fallopian tube rather than the ovary. A

dualistic model that categorizes ovarian cancer into two groups

(type I and type II) has been described. Type I tumors usually

present at a low stage and include low-grade serous, low-grade

endometrioid, clear cell, and mucinous carcinomas. Type II

tumors include high-grade serous carcinomas, high-grade

endometrioid carcinomas, carcinosarcomas, and undiferentiated

carcinomas. Type I tumors tend to be clinically indolent, whereas

type II tumors are typically highly aggressive. 154,155

Epithelial-stromal tumors can be divided into ive broad

categories based on epithelial diferentiation: serous, mucinous,

endometrioid, clear cell, and transitional cell (Brenner). 50 his

group of tumors accounts for 65% to 75% of all ovarian neoplasms

and 80% to 90% of all ovarian malignancies. he mode of spread

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