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Doppler Examination of the Normal Endometrium and Benign Endometrial Changes
Fig. 27.10 Color Doppler reveals diffuse blood flow in the thickened myometrium (“Swiss cheese” appearance) in a dysmenorrheic patient. A moderate to high RI (0.60) was recorded from the en-
dometrial tissue that had invaded the myometrium. Histology con­firmed adenomyosis.

Endometritis

27
Endometritis is characterized by a thickened endometrium that shows increased echogenicity and vascularization RI is moderately increased to 0.50 0.06 (Table 27.

Incomplete Abortion

While the value of Doppler sonography in predicting preg­nancy outcomes is still uncertain, it is clear that the use of Doppler sonography can significantly reduce uncertainties in the diagnosis of early pregnancy loss.
The manifestations of incomplete abortion vary depending on gestational age and the amount of tissue that has already been expelled at the time of examination. Ultrasound generally shows fluid and echogenic tissue fragments of varying size within the uterine cavity. Color Doppler demonstrates good
34
. The
3,
Fig. 27.11 Transvaginal scan of the uterus shows increased thickness,
echogenicity, and vascularity of the endometrium and inner third of the myometrium in a patient with endometritis. Moderate to high im-
pedance values (RI = 0.53) are measured in the corresponding vessels.
Fig. 27.
11). The clinical symptoms and vascularity tend to re-
gress over time, while the RI values remain elevated.
perfusion of gestational products that have not been expelled. The good perfusion is based on the dilatation of the spiral ar­teries and venous vessels caused by the active trophoblast.
A low vascular resistance (RI = 0.41 0.01) can be detected in the endometrium even if there is no identifiable conceptus (Table 27. and hypoechoic areas in the endometrium is still the most im­portant criterion for diagnosing incomplete abortion.
3). However, the combined presence of hyperechoic
272

Decidua

The differentiation of endometrial structures, decidual tissue, normal early pregnancy, and molar pregnancy is critically im­portant in the differential diagnosis of amenorrhea pregnancy should be considered in all patients who have a positive pregnancy test and an empty uterus with a decidual reaction or a small, central fluid collection. Color Doppler sonography is helpful in patients with nonspecific adnexal findings, as it can detect a decrease in vascular resistance on the affected side. Unlike the two concentric decidual circles of early intrauterine pregnancy, the decidual ring in an early ec­topic pregnancy consists of only one layer.
9
. Ectopic
Doppler parameters in intrauterine and ectopic pregnancies.
When Jurkovic et al. trauterine and ectopic pregnancies, they found no differences in the blood flow impedance of the uterine arteries, spiral ar­teries, and luteal vessels. However, the peak systolic velocity in the uterine arteries was identified as a parameter that very ac­curately reflects the increased blood flow in an ectopic preg­nancy. Thus, the use of transvaginal color Doppler sonography appears to be useful as an aid to therapeutic decision-making (noninterventional conservative therapy, minimally invasive surgery, or laparotomy).
21
compared the Doppler parameters of in-
References
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uterus: an old drug tested by new modalities. Ultrasound Obstet. Gynecol. 7 (1996) 374–378
2 Achiron R, Lipitz S, Frenkel Y, Mashiach S: Endometrial blood flow re-
sponse to estrogen replacement therapy and tamoxifen in asympto­matic postmenopausal women: a transvaginal Doppler study. Ultra­sound Obstet. Gynecol. 5 (1995) 411–414
3 Achiron R, Lipitz S, Sivan E, Goldenberg M, Horovitz A, Frenkel Y,
Maschiah S: Changes mimicking endometrial neoplasia in post­menopausal, tamoxifen-treated women with breast cancer: a trans­vaginal Doppler study. Ultrasound Obstet. Gynecol. 6 (1995) 116–120
4 Bohlman ME, Ensor RE, Sanders RC: Sonographic findings in adeno-
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7 Chan FY, Chau MT, Pun TC et al.: Limitation of transvaginal sonography
and color Doppler imaging in the dif ferentiation of endometrial carci­noma from benign lesions. J. Ultrasound Med. 13 (1994) 623–628
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Steinborn E, Salway J (eds.): Comprehensive gynecology. Mosby Year Book, St. Louis 1992, 545–576
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13 Exacoustos E, Zupi E, Cangi B, Chiaretti M, Arduini D, Romaninis C: En-
dometrial evaluation in postmenopausal breast cancer patients re­ceiving tamoxifen: an ultrasound, color flow Doppler hysteroscopic and histological study. Ultrasound Obstet. Gynecol. 6 (1995) 435–442
14 Fedele L, Bianchi S, Dorta M et al.: Transvaginal ultrasonography ver-
sus hysteroscopy in the diagnosis of uterine submucous myomas. Ob­stet. Gynecol. 77 (1991) 745–748
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diagnosis of diffuse adenomyosis. Fertil. Steril. 58 (1992) 94
16 Fleischer AC, Kepple DM, Entman SS: Transvaginal sonography of
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in women with postmenopausal bleeding. Brit. J. Obstet. Gynecol. 102 (1995) 133–136
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on color Doppler sonography for the evaluation of adenomyosis. J. Ul­trasound Med. 14 (1995) 529–532
19 Huang KT, Chen CA, Cheng WF et al.: Sonographic characteristics of
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20 Ismail SM: Pathology of the endometrium treated with tamoxifen. J.
Clin. Pathol. 47 (1994) 827–833
21 Jurkovic D, Bourne T, Jauniaux E, Campbell S, Collins PW: Transvaginal
color Doppler study of blood flow in ectopic pregnancy. Fertil. Steril. 57 (1992) 68–73
22 Jauniaux E, Jurkovic D, Campbell S: In vivo investigation of the anat-
omy and the physiology of early human placental circulations. Ultra­sound Obstet. Gynecol. 1 (1991) 435–445
23 Kessler A, Mitchell X, Goldberg BB: Myoma vs. contraction in preg-
nancy: differentiation with color Doppler imaging. J. Clin. Ultrasound 21 (1993) 241–244
24 Keye WR, Yuen BH, Jaffe RB: New concepts in the physiology of the
menstrual cycle. Clin. Endocrinol. Metab. 2 (1973) 251–258
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ler. J. Parinat. Med. 24 (1996) 301–317
26 Kupesic S, Kurjak A: Uterine and ovarian perfusion during the peri-
ovulatory period assessed by transvaginal color Doppler. Fertil. Steril. 60 (1993) 439–443
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son b etween Doppler velocimetry, histological and hormonal markers. Ultrasound Obstet. Gynecol. 9 (1997) 1–8
28 Kupesic-Urek S, Shalan H, Kurjak A: Early detection of endometrial
cancer by transvaginal color Doppler. EUROBS, 49 (1993) 46–49
29 Kurjak A, Kupesic S: Ovarian senescence and ist significance on uterine
and ovarian perfusion. Fertil. Steril. 3 (1995) 532–537
30 Kurjak A, Kupesic S: Transvaginal color Doppler and pelvic tumor
vascularity: lessons learned and future challenges. Ultrasound Obstet. Gynecol. 6 (1995) 1–15
31 Kurjak A, Kupesic-Urek S, Miric D: The assessment of benign uterine
tumor vascularization by transvaginal color Doppler. Ultrasound Med. Biol. 18 (1992) 645–64 9
32 Kurjak A, Kupesic S, Zalud I, Predanic M: Transvaginal color Doppler. In
Dodson MG (ed.): Transvaginal ultrasound. Churchill Livingstone, New
York 1995, 325–339
33 Kurjak A, Shalan H. Kupesic S et al.: An attempt to screen asympto-
matic women for ovarian and endometrial cancer with transvaginal color and pulsed Doppler sonography. J. Ultrasound Med. 13 (1994) 295–301
34 Kurjak A, Zalud I: The characterization of uterine tumors by transvagi-
nal color Doppler. Ultrasound Obstet. Gynecol. 1 (1991) 50–52
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nen T: Endometrial changes in postmenopausal breast cancer patients receiving tamoxifen. Obstet. Gynecol. 81 (1993) 660–664
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(1974) 239–242
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prolide acetate on uterine artery blood flow in the fibroid uterus: a prospective randomized study. Amer. J. Obstet. Gynecol. 170 (1994) 1623–1627
38 Seidler D, Laing FC, Jeffrey RB Jr, Wing VW: Uterine adenomyosis – a
difficult sonographic diagnosis. J. Ultrasound Med. 6 (1987) 345–348
39 Sheth S, Hamper VM, McCollum ME, Caskey CI, Rosenshein NB, Khur-
man RJ: Endometrial blood flow analysis in postmenopausal women: can it help differentiate benign from malignant causes of endometrial thickening. Radiology 195 (1995) 661–665
40 Siedler D, Lang FC, Jeffrey RB, Wing VW: Uterine adenomyosis—adiffi-
cult sonographic diagnosis. J. Ultrasound Med. 6 (1987) 345–349
41 Soules MR, McCarty KS Jr: Leiomyoma:steroid receptor content. Varia-
tion within normal menstrual cycles. Amer. J. Obstet. Gynecol. 143 (1982) 6–11
42 Stabile I, Grudzinkas J, Campbell S: Doppler ultrasonographic evalua-
tion of abnormal pregnancies in the first trimester. J. Clin. Ultrasound 18 (1990) 497–501
43 Thureck RW: Uterine leiomyomata. In: Garcia CR, Mastroianni L,
Amelar RD, Dubin L (eds.): Current therapy of infertility.BC Decker Inc. Toronto 1988, 80–82
44 Uziely B, Lewin A, Brufman G. Dorembus D, Mor-Yosef S: The effect of
tamoxifen on the endometrium. Breast Cancer Res. Treat. 26 (1993) 101–105
45 Vollenhoven BJ, Lawrence AS, Healy D: Uterine fibroids: a clinical re-
view. Brit. J. Obstet. Gynecol. 97 (1990) 285–298
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Gynecological Ultrasound
273
Transvaginal Color Doppler and Pulsed Doppler Diagnosis of
28
Benign Changes in the Uterine Myometrium
A. Kurjak and S. Kupesic

Examination Technique, Anatomy, and Physiology

Transvaginal color Doppler sonography can provide detailed images of the entire uterus, myometrial and endometrial changes, and the uterine vessels
Scan planes. The uterus can be imaged in three cardinal planes: long axis, semichorionic or semiaxial, and short axis long axis view is obtained by inserting the ultrasound probe into the vagina and imaging the uterus in its greatest longitudi­nal dimension. A semiaxial scan is obtained by rotating the probe 90to the long axis, delineating the full width of the
28
uterus. For the short axis view, the probe is withdrawn to the middle third of the vagina and directed toward the anterior for­nix wall.
With an anteflexed uterus, the probe handle is angled pos­teriorly to direct the beam forward. This technique is reversed for a retroflexed uterus. In a semiaxial scan of the anteflexed uterus, the cervix is the first structure to appear on the moni­tor. In a retroflexed uterus, the first structure to be visualized is the uterine fundus.
Uterine size. The normal size of the uterus varies as a function of parity and menopausal status. In nulliparae, the uterus measures approximately 6 cm in length and 3–4 cm in its an-
9
.
8, 9
. The
teroposterior and transverse diameters may measure up to 8 cm in parous women, decreasing to ap­proximately 4–6 cm after menopause.
Blood supply. The uterus derives its blood supply from a com-
plex vascular network arising from the uterine arteries. The main branches penetrate to about the outer third of the myo­metrium and form the network of arcuate arteries that encircle the uterus toward the uterine lumen myometrium and crossing the myometrial–endometrial junc­tion, they become the spiral arteries.
Contractions. The myometrial muscle fibers undergo contrac­tions during a normal menstrual cycle. Focal contractions occur in the middle or outer muscle layer during pregnancy while subendometrial contractions are common during men­struation and ovulation toward the cervix during menstrual bleeding and away from the cervix during ovulation. Presumably, contractions during the periovulatory period play an important role in sperm transport, and a deficiency of these contractions can lead to fertility problems.
4
. Smaller branches called the radial arteries run
18
. On reaching the inner third of the
1, 30
. These contractions are directed
8
. The uterine long axis
8
,
274

Leiomyomas (Fibroids)

Forms and symptoms. Uterine leiomyomas, also known as fi-
broids or myomas, are by far the most common pelvic tumors in women of childbearing age smooth muscle and sof t tissues of the uterine corpus and fun­dus. Only 3% are of cervical origin often multiple than solitary and vary greatly in size. They may be confined to the uterine musculature (intramural) or may ex­tend toward the uterine cavity, becoming submucosal. Cen­tripetal growth leads to subserous or pedunculated forms intramural type is the most common, the subserous type the least common vic pain, and infertility usually occur in patients with sub­mucous leiomyomas, while subserous leiomyomas tend to be asymptomatic. The presence and severity of symptoms corre­late closely with the number, size, and location of the tumors.
Sonographic features. The ultrasound diagnosis of leiomyomas is based on uterine contour changes, uterine enlargement, and changes in echo texture. The sonographic structure ranges
20
. Clinical symptoms such as metrorrhagia, pel-
7,20, 39
. They arise from the
26
. Leiomyomas are more
7
. The
from hypoechoic to hyperechoic, depending on the propor­tions of muscle and connective tissue. If secondary changes have developed (necrosis, intratumoral hemorrhage, degeneration, calcification), they present a broad spectrum of sonographic appearances (Fig. 28.
Leiomyomas that enlarge and outstrip their blood supply develop central ischemia, usually followed by varying degrees of degenerative change. There are reports fibroids are associated with calcifications ranging from small calcific foci to large deposits or complete calcification. Because of their variable appearance, leiomyomas may be misinter­preted as solid ovarian tumors, endometrial polyps, blood, or
8
mucus ultrasound in the detection of small submucous myomas in women who had undergone both transvaginalsonography and hysteroscopy before a scheduled hysterectomy. The sensitivity and specificity of transvaginal sonography and hysteroscopy were comparable in this study.
. Fedele et al.5investigated the accuracy of transvaginal
1).
14
that almost 25% of
Leiomyomas (Fibroids)
Fig. 28.1 Transvaginal ultrasound scan of a leiomyoma with central ischemia and necrosis.
Leiomyomas and infertility. The clinical and/or surgical man­agement of leiomyomas are directed by the symptoms and size of the palpable mass and the desire of the patient to preserve her fertility
39
. Because leiomyomas tend to occur later in a
woman’s reproductive life, the trend toward delaying parent­hood could increase the association of fibroids with infertility. Nevertheless, the relationship between these benign pelvic tumors and infertility/pregnancy failure is not yet fully under­stood. A change in the shape of the uterine cavity or an obstruc­tion of the cervix and fallopian tubes could interfere with sperm transport. Leiomyomas can also lead to venous dilata­tion, with consequent swelling of the myometrium and en­dometrium. This would impede the implantation of a fertilized ovum and might also restrict the blood supply to the develop­ing embryo. Myoma-related mehorrhagia could result from congestion and dilatation of the adjacent endometrial venous plexus, with an associated adverse effect on the myometrial, radial, and arcuate veins.
Vascularization of Leiomyomas
The blood flow impedance in small vascular branches can b e reproducibly measured with transvaginal color Doppler ultra-
16, 27
sound
with this method. Transvaginal color Doppler has been used to investigate the blood supply to leiomyomas ological and pathophysiological characteristics of blood flow in the uterine artery proved particularly helpful for the in-vivo differentiation of benign and malignant uterine tumors that benign uterine masses derive their blood supply from preexisting normal vessels (Figs. 28. color Doppler waveforms showed a slight decrease in blood flow impedance or similar perfusion patterns as in the termi­nal branches of the uterine arteries in the normal myo­metrium.
Premenopausal patients. Examinations in premenopausal
women consistently demonstrated diastolic blood flow, which
was usually increased relative to the blood flow in the uterine artery. Color Doppler also demonstrated flow at the peripher y and/or center of the leiomyoma. The mean RI of blood flow in
. Small tumor-feeding vessels are very easy to detect
23, 37
and the physi-
13,21,24,28,33,38
. Transvaginal color Doppler has
23, 27
. It has been shown
2, 28.3). Analysis of the
Fig. 28.2 Transvaginal scan of a patient with a posterior, isoechoic leiomyoma. Color Doppler shows a large-caliber vessel at the tumor periphery.
Fig. 28.3 Same patient as in Fig. 28.2. The vessel at the border of the leiomyoma is defined more clearly by power Doppler.
leiomyomaswas 0.54, and the mean PI was0.89 (Fig. 28.
4). Low
resistance indices were found in cases with necrosis and sec­ondary degenerative or inflammatory changes within the myoma (Fig. 28.
5).
In our own studies of patients with leiomyomas and healthy volunteers, the same technique was used to investigate blood flow in the uterine arteries. In patients with leiomyomas,
we found increased blood flow velocities and decreased RI and
PI values in both uterine arteries (Fig. 28.
6). The different
vascularization patterns observed in this study could be useful
in predicting the growth rates of these benign uterine tumors.
Postmenopausal patients. Several interesting observations
were made in women with shrunken fibroids after
menopause
33
. The blood flow at the periphery of the tumors showed a higher RI than in premenopausal women, and some cases showed a complete absence of end-diastolic blood flow.
Transvaginal color Doppler can also be used to evaluate the ef­fect of hormone replacement therapy on the thickness of the endometrium and myometrium. Moreover, Doppler examina­tions can supply additional information on the quality of blood flow in the uterine, myometrial, and endometrial vessels. It can be used to assess the effect of treatment measures on uterine morphology and perfusion and even answer the question of
whether hormone replacement therapy increases the risk of a myometrial neoplasm.
Gynecological Ultrasound
275
Transvaginal Color Doppler and Pulsed Doppler Diagnosis of Benign Changes in the Uterine Myometrium
Fig. 28.4 Same patient as in Figs. 28.2 and 28.3. The Doppler spec-
trum indicates a moderate RI (0.59). Histopathology confirmed the
benign nature of the tumor.
28
Fig. 28.6 A giant intramural leiomyoma has caused a significant fall
of vascular resistance in the uterine arteries (RI = 0.61).
Fig. 28.5 Pulsed Doppler signals from a small vessel at the border of
the leiomyoma indicate a small variation between systolic and end-di­astolic blood flow (RI = 0.52).
Fig. 28.7 Transvaginal scan of a subserous leiomyoma. The color Doppler image shows normal branching of the vessels arising at the periphery of the uterus. The spectral trace indicates moderate to high impedance in the tumor vessels (RI = 0.61).
276
Differentiation from ovarian tumors. Color Doppler sonogra­phy is useful in differentiating intraligamentous fibroids from solid ovarian tumors (Fig. 28.
7). Even if the uterine tumor is lo-
cated outside the uterine corpus, Doppler can still reveal waveforms that are typical of the uterine vascular network. The flow pattern in these cases generally resembles the pattern of normal myometrial blood flow arising from the terminal branches of the uterine arteries. By contrast, the vessels that supply adnexal tumors are derived from the ovarian vessels.
Leiomyomas during pregnancy. Since leiomyomas are respon­sive to female sex hormones, they frequently enlarge during
early pregnancy
29, 36
. Transvaginal color Doppler sonography is the method of choice for observing hemodynamic changes in the maternal and fetal vascular system of the placenta, both in normal early pregnancies and in pregnancies with uterine fi-
19,22, 25
broids
. No significant difference in blood flow im­pedance (p 0.05) was observed between the two groups. Leiomyomas affect neither the hemodynamics of the utero­placental circulation nor the maternal or fetal components of the placental circulation. The marked rise of blood flow veloc­ity measured in the radial arteries from the 10th to 13th weeks of gestation (p 0.001) is probably due to the increased me­tabolism of the growing fibroid cells.

Management of Uterine Leiomyomas and the Importance of Color Doppler Sonography

Management of Uterine Leiomyomas and the Importance of Color Doppler Sonography
Current treatment options for uterine fibroids include nonsur­gical therapies (especially the use of gonadotropin-releasing hormones, GnRH agonists) as well as various surgical options such as abdominal, laparoscopic, or hysteroscopic myom­ectomy and abdominal or vaginal hysterectomy (which may be laparoscopy-assisted).
Medical Treatment with GnRH Agonists
Mechanism of action. Hormonal therapy is best for reducing
the size of submucous leiomyomas to relieve postoperative symptoms, facilitate hysteroscopic resection, or temporize until menopause in perimenopausal women. Synthetic GnRH agonists inhibit estrogen production, leading to a decrease in uterine size. Filicori et al.
with uterine fibroids and anemia who was treated with GnRH agonists. Since then, many studies have been publishe d con­firming the efficacy of GnRH agonistsin reducing the size of the uterus and leiomyomas and suppressing menstrual bleeding.
Reduction in uterine volume. Friedman10documented an average
40–50% reduction of uterine volume relative to pretreatment size in women who were treated with GnRH agonists for 3–6 months. Generally the decrease in uterine volume was greatest during the
first 12 weeks of therapy. More than a 50 % reduction in uterine
volume was achieved in 20% of the women, and a moderate reduc-
tion of 26–50 % was achieved in half of the women. A slight reduc-
tion of up to one-fourth the pretreatment size was obtained in 25 % of the women, and in 5% the uterus enlarged by up to 25% of the pretreatment size. GnRH agonists did not continue to afford pro-
tection after they were discontinued. The myomas generally re-
turned to their original size within four months after the end of
treatment.
Measurement of RI. The first Doppler examination of the uterine arteries in fibroid patients treated with GnRH agonists was per-
formed by Matta et al. in 1988 eight patients, showed a significant rise of resist ance in the uterine
vessels after four months’ treatment with GnRH agonists. During
that time the RIs were measured in the uterine arteries and in the larger fibroid vessels. After treatment, the RI rose significantly from an average of 0.52 in the uterine arteries and 0.48 in the fibroid ar-
teries to respective values of 0.92 and 0.91. The authors concluded
that a decrease in uterine vasculature was responsible for the re­duction in uterine volume after treatment with GnRH agonists.
Effect of RU 486 and leuprolide acetate. Reinsch et al. studied the effect of RU 486 (mifepristone, a synthetic steroid with both antiprogesterone and antiglucocorticoid properties) com­pared with leuprolide acetate on uterine blood flow in 14 women. Both groups showed a rise of RI values in the uterine arteries and a reduction in uterine volume following three months’ treatment.
The RI rose in 2–51% of the patients who had received RU 486 and in 8–39% of the patients treated with leuprolide acetate. The authors interpreted the rise of RI in response to GnRH agonist therapy as a hypoestrogenic effect, while the decreased blood flow in response
to RU 486 was apparently caused by other, previously unknown mechanisms.
Our studies. In one study we observed 25 women with sympto­matic uterine leiomyomas, 88% of whom complained of metrorrha-
6
were the first to report on a patient
33
. Their study, which involved only
35
recently
gia, 52 % of lower abdominal pain or pressure, and 40 % of dys­menorrhea. We performed transabdominal and/or transvaginal sonography in these patients to examine the uterus and adnexa.
The volume of the myomas was calculated using the formula for an ellipsoid (0.521length width depth). Pulsed and color Dopp­ler ultrasound were used to identify and quantitate blood flow in
the main arteries supplying the myomas. The initial tumor volumes
were between 25 and 390 mm amination, 1200 ministered intranasally. Transvaginal color Doppler examinations
were performed for follow-up during and at the end of GnRH ana­logue therapy. The mean RI in the principal myoma-feeding vessels
was 0.54 0.08. The resistance in these vessels rose markedly during the first three months of treatment to a mean RI of 0.78,
while the myoma volume decreased to 76% of the initial value.
After six months’ treatment, the mean myoma volume had been re­duced to 56% of the pretreatment volume, with color Doppler showing a rise of impedance to RI = 0.88 in the uterine arteries and RI = 0.82 in the myoma vessels in 80% of the patients treated.
We also observed that three myomas disappeared completely and had not recurred by six months after the end of treatment. The remaining myomas increased their volume by 24% of the initial posttreatment size. Nine of the 25 patients were referred for surgi­cal treatment with improved hemoglobin levels. The reduced uterine and myoma volumes, which now enabled operative treat­ment, resulted in less intraoperative blood loss, facilitated enuclea-
tion of the myomas, and reduced the number of postoperative complications metrorrhagia experienced menopause during the therapy.
µg/day of buserelin (Suprefact, Höchst) was ad-
31, 32
. Four perimenopausal patients with severe
3
(mean value 85 mm3). After this ex-
Surgical Treatment
Methods. The surgical treatment options for uterine leiomyo-
mas include abdominal, laparoscopic, and hysteroscopic myo­mectomy as well as abdominal and vaginal hysterectomy. The main advantage of myoma enucleation is that it preserves the uterus and thus the patient’s fertility.No benefit has been dem­onstrated for laparoscopic removal, however. Several pub­lished cases document possible complications including uterine suture dehiscence treatment for symptomatic uterine fibroids in women who have concluded their childbearing. The mortality risk of hys­terectomy for a benign indication is approximately 1 : 1000
Laser therapy. A small study34described a very promising alterna-
tive to the above surgical treatments for uterine fibroids: laparo­scopic myolysis with the Nd:YAG laser. The laser applicator was in-
troduced laparoscopically into the myoma. During treatment, the applicator was repeatedly inserted into the leiomyoma to reduce
the stroma, denature tumor proteins, destroy tumor vessels, and reduce the tumor volume. The insertion sites were spaced 5–7 mm apart, and the blood vessels at a 3–5 mm radius around each inser-
tion site were coagulated. Multiple punctures were effective in ob­literating the myomas. Since the uterus remains fully intact, there is no impairment of hormonal or sexual function. At six-month follow­up, the echo structure of the coagulated myomas so closely re­sembled normal myometrium that only an experienced examiner could tell the difference. A long-term study of seven patients showed no evidence of tumor regrowth. Histological examination showed complete devascularization of the myoma tissue with sub­sequent necrosis
34
.
15
. Hysterectomy is the definitive
2, 40
Gynecological Ultrasound
.
277
Transvaginal Color Doppler and Pulsed Doppler Diagnosis of Benign Changes in the Uterine Myometrium
Electrocautery. Currently we are completing a study to evaluate
the size, vascularity, and degenerative changes in myomas whose
feeding vessels were electrocoagulated by the laparoscopic route. Color Doppler ultrasound was used to demonstrate the myoma ves­sels during the electrocautery. Accurate spatial placement of the bipolar needles in the vascularized plane of the myoma was com­pared with “blind” electrocautery. We believe that the treatment can be made more successful and the procedure shortened with
the aid of color Doppler.
We therefore investigated key variables such as the amount of
bleeding and the reduction in myoma size following laparoscopic
electrocautery in one group of patients in which color Doppler had been used and another group in which the entire myoma had been “blindly” coagulated. We found that the size and vascular supply of
the myomas showed a much greater regression in the color Dopp­ler group than in the group without color Doppler guidance. These initial results underscore the value of color Doppler sonography in
the management of leiomyomas, not only to better document le­sion size and structure but also as an aid to preoperative planning and intraoperative guidance for resection or electrocautery.

Vascular Diseases in the Lesser Pelvis (Varicose Veins or Arteriovenous Malformations)

These lesions are easily demonstrated by duplex sonography or color Doppler imaging
17
(Figs. 28.8, 28.9). Doppler sonogra­phy is the modality of choice for distinguishing these vascular lesions from cystic structures without internal echoes such as hydrosalpinx and from cysts diagnosed by B-mode imaging (Figs. 28.
10– 28.12).
Uterine adenomyosis is discussed in Chapter 27 (Doppler Examination of the Normal Endometrium and Benign En­dometrial Changes).
28
278
Fig. 28.8 Color Doppler image (right) reveals a dilated uterine vein in
the outer third of the myometrium.
Fig. 28.10 Transvaginal sonogram shows ir­regular structures near the uterus of a
woman with chronic lower abdominal pain. A definitive diagnosis could not be made from the B-mode image.
Fig. 28.11 Same patient as in Fig. 28.10. The color Doppler image shows dilated pelvic veins consistent with pelvic congestion syn­drome.
Fig. 28.9 Color Doppler is the method of choice for diagnosing pelvic
congestion syndrome.
Fig. 28.12 Same patient as in Figs. 28.10 and 28.11. Appearance of the dilated pelvic
veins in the power Doppler mode.
References
References
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Gynecological Ultrasound
279
Use of Color Doppler in the Evaluation of
280
29
Suspicious Endometrial Findings
M. Holländer, C. Villena-Heinsen, A. K. Ertan, and W. Schmidt

Incidence of Endometrial Carcinoma

Endometrial carcinoma has become the most common tumor of the female genital tract. While the incidence of cervical cancer is definitely on the decline, owing largely to effective Pap screening programs, the incidence of endometrial cancer is slightly on the rise. The rate of new cases in Saarland, Germany, during the 1970 s and 1980 s was between 20 and 30 per
100,000 population, or approximately 15 cases per 100,000

Diagnostic Investigation of Suspicious Endometrial Findings

29
Transvaginal sonography. Malignancy should be suspected in women with postmenopausal bleeding or other bleeding ir­regularities and when thickened or irregular endometrium is noted at ultrasound. There is no question that transvaginal sonography has added much new information to endometrial examinations compared with transabdominal scanning. On closer scrutiny, however, we find that vaginal sonography is in­accurate in a considerable number of the cases examined and that different authors have cited very different cutoff levels for endometrial thickness at which curettage is urgently indi­cated, ranging from sensitivity and specificity data are not sufficient to eliminate the need for histological evaluation fractional curettage is still the “gold standard” for excluding cancer in women with postmenopausal bleeding or sono­graphic abnormalities, even though endometrial cancer is ac­tually found in only a small percentage of cases necessary biopsies in this predominantly older population with an increased surgical risk, noninvasive methods are being sought that can differentiate benign endometrial changes from carcinoma.
4 mm
10
to as much as 10mm23. At present,
6, 22, 31, 33, 34, 43
. As a result,
9, 32
. Toavoid un-
Color Doppler Sonography
Neovascularization of tumors. The hope that color Doppler
sonography will yield additional diagnostic information is based on the following theoretical considerations. Solid tumors have the capacity to induce angiogenesis, and they re­quire these newly formed vessels in order to grow new vessels have a distinctive histological morphology: they are dilated, saccular, and tortuous with arteriovenous shunts and intervenous connections. The vessel walls contain very little smooth muscle, giving the vessels a lower impedance to flow than “normal” arterioles. This results in a markedly lower flow velocity
15, 20, 28, 37
.
13, 14
. These
based on the World Standard Population in obese postmenopausal women, with a peak age incidence of 60–65 years (normally distributed) are diabetes mellitus, arterial hypertension, infertility, unop­posed estrogen use, tamoxifen therapy, and genetic pre­disposition
Doppler parameters. Color Doppler is being used in an attempt
to detect this altered flow pattern. Waveforms are recorded to derive objective parameters that may be useful for noninvasive benign–malignant discrimination. Because absolute flow velocity depends on the incidence angle of the color Doppler beam and an accurate angle correction often cannot be made, it is better to use standard angle-independent parameters that indicate flow resistance: the S/D ratio, the resistance index (RI) = (S–D)/S, or the pulsatility index (PI) = (S –D)/mean, where S = maximum frequency shift in systole, D = minimum frequency shift in diastole, and mean = mean value.
Breast and ovarian cancers. The Doppler examination of blood
vessels has already been applied to the differential diagnosis of other gynecological tumors, particularly breast and ovarian cancers. With regard to ovarian cancer, initial studies reporting extremely positive results studies giving reports of poor accuracy and specificity Contradictory studies have also been published on breast cancer diagnosis. While Sohn in 1992 found a statistically sig­nificant decline of maximum resistance indices in breast cancers compared with benign tumors and Madjar in 1994 noted higher velocity sums in breast malignancies, the work­ers at our center were unable to confirm these positive results either as discriminatory parameters or as a means of assessing breast cancer prognosis
Endometrial findings. In the early 1990s, the first studies ap-
peared on the use of color Doppler sonography in the differen­tial diagnosis of endometrial pathology. The authors initially limited their work to large-vessel examinations such as that of the uterine artery sels in the endometrium and also in tumors. Most of the stud­ies analyzed the angle-independent parameters RI and/or PI, since the sampled vascular segments are often very short and precise angle correction is difficult to achieve.
11,16,19,40
24
. The risk is highest
24
. Additional risk factors
.
17, 26
gave way to increasingly critical
41
.
4, 5, 21
, but soon they also studied smaller ves-
38, 39
.

Experience at the Department of Obstetrics and Gynecology, Homburg University Hospital, Saar

Examination of the Uterine Artery

Several authors found significant differences in flow resistance between benign and malignant endometrial lesions. Bourne et
4
al.
stated a cutoff value of PI = 2.0 for the uterine artery. Chan
8
et al.
also found significant PI differences, but only between normal and abnormal endometrium; benign lesions could not be distinguished from their malignant counterparts. The authors used a higher cutoff value than Bourne et al., with
PI
= 2.17 for endometrial carcinoma. Similarly, Merce
mean
could distinguish only between normal endometrium and en­dometrial disease (i.e., benign and malignant changes). Kupesic-Urek examined both the uterine artery and en­dometrial vessels uterine artery resistance indices were considerably less than those reported by Merce (Table 29.
Table 29.1 Review of the literature on uterine artery examinations, with significant results
Author Number Vessel Indices for
malignant
Indices for benign lesions
lesions
Bourne 1990
4
54 Uterine artery/
PI
= 0.89 PI
mean
= 3.82 Cutoff value: PI = 2.0
mean
(endometrium) Bourne 1991 Mercé 1991
5
30
Kupesic-Urek 1993
Chan 1994
a
Includes different groups with benign pathology.
b
No distinction made between malignant and benign pathology, only between normal and abnormal.
8
138 Uterine artery PI
64 Uterine artery/
myometrial
25
276 Uterine artery
endometrial
67 Uterine artery PI
= 0.91 PI
mean
RI
= 0.79
mean
RI = 0.66 RI = 0.53
RI = 0.37
=2.17 A:PI
mean
2.53
mean
RI
0.87
mean
RI 0.78 RI = 0.76
RI = 0.54
mean
B: PI
mean
25
= 3.41 = 2.28
and found significant differences. The
1).
Analysis
a
(b) Statistically significant
Statistically significant
A: normal, B: benign pathology; signi­ficant differences between A and B and
between A and cancer
30
Gynecological Ultrasound
Experience at the Department of Obstetrics and Gynecology, Homburg University Hospital, Saar
tors for endometrial cancer (obesity, diabetes mellitus, arterial
Patients and Methods
We studied 95 women from 17 to 88 years of age (average 57.8
years) with clinically suspicious (menorrhagia, metrorrhagia, postmenopausal bleeding) or sonographically suspicious (structure, diameter) endometrial findings who had been re­ferred to our department for further evaluation.
Sonographic and color Doppler sonographic examinations. All patients underwent hysteroscopic biopsy or fractional curet­tage to establish a histological diagnosis. The surgery was preceded by a transvaginal B-mode ultrasound examination of the internal genitalia with assessment of endometrial diame­ter and structure. This was immediately followed by a color Doppler examination to determine whether endometrial and subendometrial blood vessels could be visualized and, if so, how many. We also attempted to record a frequency-shift
waveform from each endometrial vessel that could be visual­ized. These waveforms were then used to determine the angle­independent parameters of S/D ratio, RI, and PI along with the smallest value (min), greatest value (max), and mean value (mean) for each patient. We also documented menopausal sta­tus, the use of hormonal products, and the presence of risk fac-
hypertension, positive family history). All examinations were performed with an Acuson 128 XP/10 scanner with integrated color Doppler using a 5 MHz endovaginaltransducer that could be switched to 5 MHz pulsed color Doppler mode. The scanner
was operated over a power range of 50–500 mW/m sensitivity was set to the lowest velocity range. For maximum sensitivity in locating vessels, the color Doppler gain was set just below the noise threshold.
Fractional curettage. Nineteen of the women (20%) were pre­menopausal, 62 (65.3 %) were postmenopausal, and 14 (14.7%)
were perimenopausal. The indication for curettage was a bleeding disorder (postmenopausal bleeding, menorrhagia, metrorrhagia) in 74.8% of the patients and suspicious en­dometrial findings in 16.8%. Other causes (lower abdominal pain, search for a primary tumor, etc.) were present in 8.4%. Ex­amination of the curettage material revealed a malignant con­dition in 23 cases (24.2 %) and a benign condition in 72 cases (75.8%). As expected, the great majority of cancer patients (87%) were in menopause. A histological breakdown of the malignant lesions revealed 21 adenocarcinomas, one müllerian mixed tumor, and one high-sited cervical carcinoma (Tables 29.
2 and 29.3).
2
, and color
281