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Radiol Clin N Am 42 (2004) 297 314

Sonographic evaluation of first-trimester bleeding


Raj Mohan Paspulati, MD*, Shweta Bhatt, DMRD, DMRE, Sherif Nour, MD
Department of Radiology, University Hospitals of Cleveland, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH 44106, USA

Vaginal bleeding in the first trimester of pregnancy is a common presentation in emergency care facilities. About 25% of all gestations present with vaginal spotting or frank bleeding in the first few weeks of pregnancy; half of these progress into miscarriage or abortion [1]. The acuity of these symptoms may vary from occasional spotting to severe hemorrhage, associated with cramping and abdominal pain. The bleeding often is self-limited and is most likely caused by implantation of the conceptus into the endometrium. The important causes of first-trimester bleeding are spontaneous abortion, ectopic pregnancy, and gestational trophoblastic disease. The clinical assessment of pregnancy outcome is unreliable and ultrasound (US) evaluation combined with quantitative beta human chorionic gonadotropin (b-hCG) is an established diagnostic tool in these patients. This article reviews the role of ultrasonography in the evaluation of patients presenting with first-trimester bleeding.

Sonographic anatomy The uterus is a pear-shaped, muscular organ that varies greatly in size and shape depending on age and prior pregnancies. The normal postpuberty uterus in an adult measures approximately 7.5 to 8 cm in length, 4 to 5 cm in width, and about 2 cm in anteroposterior dimension. The normal cervix is 3.5 to 4 cm in length. The cervix is comprised of internal

* Corresponding author. E-mail address: paspulati@uhrad.com (R.M. Paspulati).

and external cervical os. The internal os is the junction of the uterine cavity and the cervical canal and the external os is the junction of the cervical canal and the vagina. Transvaginal US (TVUS) of the normal myometrium reveals three distinct layers. Arcuate vessels separate the thin outer layer from the thick middle layer, and both layers are homogeneous with the outer layer more hypoechoic relative to the middle layer [2]. The inner layer consists of a thin hypoechoic halo that surrounds the endometrium and corresponds to the junctional zone seen on MR imaging. The endometrial thickness measurements are optimally made on sagittal (long-axis) images of the uterus; this measurement should be performed on the thickest portion of the endometrium excluding the hypoechoic inner myometrium (Fig. 1). The endometrial thickness should be reported as the double thickness measurement [3]. If endometrial fluid is present, its diameter should be omitted; in such cases the endometrial thickness should be reported as the sum of the measurements obtained from the anterior and posterior endometrial walls. An endometrial thickness of 4 to 14 mm is normal in an adult premenopausal woman. Endometrial thickness and appearance vary with the phase of the menstrual cycle [4]. The position of the ovaries is variable but they are usually found in the posterior fold of the broad ligament, posterior and distal to the fallopian tubes. On sonography the ovaries can be localized anterior to the internal iliac vessels. The postpubertal ovary measures approximately 3 cm in length, 2 cm in width, and 1 cm in anteroposterior dimension. The upper limit for normal ovarian volume is highest in young adult women measuring approximately 9.8 to 14 mL and declines with increasing age [5]. Normal

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ler US in early pregnancy, the concept of as low as reasonably achievable is important [7] and the advantages of the Doppler US should outweigh the potentially harmful effects on the conceptus.

Normal first-trimester sonography Scanning in the first trimester may be performed either transabdominally or transvaginally. TVUS is preferred and is the community standard. The firsttrimester milestones are given in Tables 1 and 2. A gestational sac can be identified with TVUS at 5 weeks of gestational age, when it measures 5 mm. The yolk sac should always be seen by TVUS when a gestational sac measures greater than 10 mm and by transabdominal US when the mean sac diameter is greater than 20 mm [8,9]. An embryo with cardiac activity should be seen transvaginally when the gestational sac measures greater than 18 mm, and transabdominally when the gestational sac measures 2.5 cm. These discriminatory criteria should be used as guidelines. If the findings of the US examination are equivocal and the examination is technically difficult, a follow-up examination should be obtained. Gestational sac The blastocyst implants into the endometrium by approximately 23 days of menstrual age [10]. It measures 0.1 mm and is too small to be visualized on TVUS. Demonstration of peritrophoblastic flow by transvaginal color flow Doppler at this focal decidual thickening has improved the diagnostic sensitivity of intrauterine pregnancy (IUP) from 90% with TVUS alone to 99% using transvaginal color flow Doppler [11,12]. The peritrophoblastic flow has a characteristic high-velocity and low-impedance flow caused by shunting of blood from the spiral arteries into the intervillous spaces. According to Emerson et al [11], the peak systolic velocity of peritrophoblastic flow in a normal IUP ranges from 8 to 30 cm/second, before the visualization of the gestational sac. Yeh et al

Fig. 1. Sagittal TVUS of the uterus demonstrates a normal endometrial lining (arrowheads).

fallopian tubes cannot be visualized with current US imaging equipment

Scanning technique Ultrasound evaluation of the female pelvis is conducted with a real-time scanner, preferably using a sector or curvilinear transducer. The scanner is adjusted to operate at the highest clinically appropriate frequency, realizing that there is a trade-off between the resolution and beam penetration. Transabdominal pelvic US is performed with a full bladder using transducer frequencies of 3.5 MHz and above. Adequate distention of the bladder displaces the bowel from the field of view. Transabdominal US gives an initial overview of the uterus, adnexa, and any intra-abdominal free fluid. TVUS is performed with the patients bladder being empty, using a transducer frequency of 5 to 7.5 MHz. TVUS gives detailed information about the uterus and the adnexa. Higher-frequency transvaginal probes can be positioned closer to the pelvic organs resulting in improved spatial resolution and diagnostic accuracy. Currently available transducers of 10 MHz and above can identify the finer details of intrauterine gestation and have greatly contributed to the early diagnosis of abnormal gestation and to the management of firsttrimester bleeding. Color flow Doppler and pulsed Doppler may be added to the examination, as indicated by the gray-scale US findings. It is important to bear in mind that the energy output of Doppler US is substantially higher than that used for imaging and it may have potentially harmful effects on the conceptus [6]. Because of this risk, caution has been expressed over the routine use of Doppler US in early pregnancy evaluation. While performing Dopp-

Table 1 First-trimester scanning milestones Parameter Gestational sac Yolk sac Transabdominal US Transvaginal US Present at 5 wk (5 mm) Always present when GS > 10 mm GS > 18 mm

Always present if GS > 20 mm Cardiac activity GS > 2.5 cm

Abbreviations: GS, gestational sac; US, ultrasound.

R.M. Paspulati et al / Radiol Clin N Am 42 (2004) 297314 Table 2 Land marks of normal first-trimester pregnancy Gestational age 23 d 3.5 4 wk 4 4.5 wk 4.5 5 wk 5 5.5 wk Embryologic change Blastocyst implantation Decidual changes at implantation site Trophoblastic tissue Exocoelomic cavity of the blastocyst Secondary yolk sac Sonographic appearance Blastocyst measures 0.1 mm and is too small to visualize Focal echogenic decidual thickening at implantation site

299

5 6 wk 5 6 wk

Embryo Embryonic cardiac activity

High-velocity and low-impedance trophoblastic flow at the implantation site on TVCFD Gestational sac (a sonographic term) is always seen when it measures > 5 mm and the serum b-hCG is between 1000 and 2000 mIU/mL (IRP) Yolk sac is seen as a thin-walled cystic structure within the gestational sac and should always be seen when the GS is > 10 mm; it is the first sign of a true gestational sac before the visualization of embryo Seen as a focal echogenic area adjacent to the yolk sac; should always be seen when the GS is > 18 mm Embryonic cardiac activity should always be seen when the embryo is > 5 mm; normal heart rate ranges from 100 115 beats/min between 5 6 wk of gestation

Abbreviations: CG, human chorionic goradotropin; GS, gestational sac; IRP, international reference preparation; TVCFD, transvaginal color flow Doppler.

[13] described a focal, eccentric, anechoic area in the endometrium caused by the embedded blastocyst as the intradecidual sign. They described this sign as early as 3.5 weeks of menstrual age on transabdominal US and reported a sensitivity rate of 92%, a specificity rate of 100%, and an accuracy rate of 93%. Laing et al [14] used TVUS to demonstrate this sign and found that the overall sensitivity, specificity, and accuracy for the intradecidual sign were only 48%, 66%, and 45%, respectively. With currently available high-frequency transvaginal probes, a gestational sac as small as 2 to 3 mm can be demonstrated at 4 weeks of gestational age [15 17]. On TVUS, the gestational sac is seen as a well-defined fluid-filled cavity with a surrounding hyperechoic rim, embedded eccentrically in the endometrial lining of the fundus or midbody of the uterus (Fig. 2). The sonographic term gestational sac represents the exocoelomic cavity of the blastocyst and the surrounding echogenic rim is caused by the developing chorionic villi and decidual tissue. The echogenic rim should have a minimum thickness of 2 mm and its echogenicity should exceed that of myometrium [1]. The double decidual sac sign of intrauterine gestation was first described in 1982 [18]. The double decidual sac sign consists of two concentric echogenic rings encasing a central anechoic focus that impress on the endometrial stripe. The inner echogenic rim represents the decidua capsularis and chorion laeve, whereas the outer echogenic rim represents the decidua parietalis; these echogenic rims are separated by a thin rim of fluid in the endometrial cavity (Fig. 3). This is a useful sign of IUP between 4 and 6 weeks of gestation. The crown-rump length (CRL)

of the embryo is a more accurate indicator of gestational age than the mean gestational sac diameter. The mean gestational sac diameter should be recorded, however, when an embryo is not identified. Because hCG production and gestational sac growth are related to trophoblastic function, there is excellent correlation of the serum hCG level, sac size, and the stage of pregnancy [19]. Kadar et al [20] first introduced the concept of a discriminatory level of the b subunit of hCG. The range of the serum b-hCG level at which an intrauterine gestational sac is visualized is the discriminatory zone. Although the discriminatory range of b-hCG varies from one laboratory to another, the widely accepted range is from

Fig. 2. Coronal TVUS of the uterus shows a gestational sac with hyperechoic margins (arrow) and endometrial cavity (curved arrow).

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Fig. 3. Double decidual sac sign. (A) Coronal TVUS of the uterus reveals an intrauterine gestational sac (straight arrow), decidua capsularis (curved arrow), decidua parietalis (arrowhead), and effaced endometrial cavity (asterisks). (B) Corresponding line diagram.

1000 to 2000 mIU/mL international reference preparation (IRP) for TVUS and 2400 to 3600 mIU/mL (IRP) for transabdominal US [10]. In normal pregnancy serum b-hCG should double or increase by at least 66% in 48 hours. Yolk sac The first structure to be seen within the gestational sac is the secondary yolk sac, which is a reliable indicator of a true IUP with a positive predictive value of 100%. The primary yolk sac is not seen by US because it shrinks at 4 weeks menstrual age and gradually disappears with the formation of the secondary yolk sac [21]. The secondary yolk sac is first seen on TVUS as a thin-walled cystic structure by the fifth gestational week and is virtually always seen by 5.5 weeks gestational age (Fig. 4) [22]. The yolk sac is round, measures less than 6 mm, and should be visualized by TVUS when a gestational sac measures more than 10 mm [10]. The yolk sac is involved in nutritive, metabolic, hemopoietic, and secretive functions during early embryonic development and organogenesis [23,24]. Abnormalities in its size and appearance are predictors of abnormal gestation [25]. Embryo The embryo should always be visualized by TVUS when the gestational sac measures greater than 18 mm, and transabdominally when the gestational sac measures 2.5 cm (Fig. 5). With the currently

available high-frequency transvaginal transducers, the embryonic disk is initially seen as a focal echogenic area of 1- to 2-mm thickness adjacent to the yolk sac between 5 and 6 weeks of gestational age [26 29]. Embryonic cardiac activity should always be seen when an embryo measures greater than 5 mm. Occasionally the heartbeat may be seen adjacent to the yolk sac even before the embryo is clearly visible.

Fig. 4. TVUS of the uterus demonstrates a yolk sac (thin arrow) outside the amniotic membrane (arrowhead), which has not yet fused with the chorion (curved arrow). Embryo (thick arrow) is seen within the amniotic sac.

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branes before 14 weeks of gestation is considered normal (see Figs. 4 and 5).

Spontaneous abortion Spontaneous abortion is defined as pregnancy terminating before the 20th completed week of gestation. Approximately 80% of spontaneous abortions occur in the first trimester. The causes of spontaneous abortions fall into two categories: genetic and environmental (maternal) as listed next:
Fig. 5. TVUS of the uterus shows a normal embryo and separate amniotic membrane (arrow) in close relation to the embryo. This should not be mistaken for nuchal translucency.

Levi et al [3] suggested a 4-mm CRL cutoff because their study demonstrated cardiac activity in all embryos with a CRL of 4 mm [30]. Other studies demonstrated 5 mm as the discriminatory CRL for detecting cardiac activity [31,32]. Although visualization of a living embryo does not ensure a viable pregnancy, the abortion rate decreases for living embryos as the gestational age increases, with a 0.5% demise rate for living embryos between 6 and 10 mm [33]. If the length of the embryo is less than 5 mm, follow-up US should be performed until the expected CRL exceeds the discriminatory value. Most of the studies reported a heart rate of 100 to 115 beats per minute between 5 and 6 weeks [34 36]. By 9 weeks of gestational age, the mean heart rate increases to about 140 beats per minute. The cardiac activity should be documented by M-mode. Amniotic sac The amniotic sac is formed in the fourth week of gestation between the ectoderm layer and the adjacent trophoblast. Before 6.5 weeks the amniotic membrane is so close to the embryo that the amniotic cavity around the embryo is not easily seen. The diameter of the amniotic cavity is nearly equal to the CRL. Between 5 and 7 weeks of gestational age the embryo is located between the amniotic and yolk sacs. On US, this amniotic sac embryo yolk sac complex appears as two small sacs and is called the double bleb sign [9]. The embryo and the inner amnion grow at a faster rate than the outer chorionic cavity with eventual fusion of the amniotic and chorionic membranes by 16 weeks of gestation [37]. Separation of the amniotic and chorionic mem-

Genetic or fetal causes Trisomy Polyploidy or aneuploidy Translocations Environmental or maternal causes Uterine Congenital uterine anomalies Leiomyoma Intrauterine adhesions or synechiae (Ashermans syndrome) Endocrine Progesterone deficiency (luteal phase defect) Hypothyroidism Diabetes mellitus (poorly controlled) Luteinizing hormone hypersecretion Immunologic Autoimmunity: antiphospholipid syndrome, systemic lupus erythematosus Infections Toxoplasma gondii, Listeria monocytogenes, Chlamydia trachomatis, Ureaplasma urealyticum, Mycoplasma hominis, herpes simplex, Treponema pallidum, Borrelia burgdorferi, Neisseria gonorrhoeae Genetic abnormalities are the most common cause of spontaneous abortions accounting for almost 50% to 60% of cases. Autosomal trisomy is the most frequently identified chromosomal abnormality resulting in first-trimester abortions. The incidence of abortions secondary to chromosomal abnormalities markedly increases after the maternal age of 35 years. The environmental or maternal causes account for a small percentage of spontaneous abortions. These include infection; anatomic defects (maternal mullerian defects); endocrine factors (failure of corpus luteum); immunologic factors (antiphospholipid antibody syndrome); and maternal systemic disease (diabetes mellitus, hypothyroidism). The algorithmic approach to first-trimester bleeding is summarized in Fig. 6.

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First Trimester Ultrasound


Embryo not visualized

MSD > 18MM

MSD < 18MM

YS present

YS absent

MSD < 10MM

MSD > 10MM

ED ED
F/U re: sac growth and embryo 1

B
Embryo visualized

Cardiac activity present

Cardiac activity absent

CRL > 5MM

CRL < 5MM

CRL > 5MM

CRL < 5MM

YS present

YS absent

YS normal

YS abnormal

MSD-CRL > 5MM

MSD-CRL < 5MM

HR N

HR AbN

? F/U 18 wks 1

F/U 2

F/U 2wks re: growth and cardiac activity 1

ED

F/U re: growth and cardiac activity 1

Fig. 6. (A, B) Proposed algorithms for evaluating women with first trimester bleeding. ED, embryonal demise; F/U, follow-up; HR ABN, heart rate abnormal; HR N, heart rate normal; YS, yolk sac. (From McGahan J, Goldberg B. Diagnostic ultrasound: a logical approach. Philadelphia: Lippincott, Williams & Wilkins; 1998; p. 142 3; with permission.)

The most common morphologic finding in early spontaneous abortions is an abnormality of development of the zygote, embryo, early fetus, or the placenta. Spontaneous abortion is clinically classified into threatened, inevitable, missed, incomplete, and complete abortions (Table 3).

Ultrasound findings in abortion The US findings depend on the developmental stage of the pregnancy at which the patient presents with symptoms. Familiarity with normal sonographic landmarks of first-trimester pregnancy is essential

R.M. Paspulati et al / Radiol Clin N Am 42 (2004) 297314 Table 3 Classification of spontaneous abortion Types Threatened abortion Clinical features Vaginal bleeding before 20 wk gestation without cervical dilatation Vaginal bleeding with partial expulsion of products of conception before 20 wk gestation and cervical dilatation Embryonic demise before 20 wk of gestation without expulsion of products of conception; may or may not have vaginal bleeding Vaginal bleeding and expulsion of all products of conception before 20 wk gestation Vaginal bleeding before 20 wk gestation with cervical dilatation US findings

303

Incomplete abortion

Depending on the stage of pregnancy, US may show an empty uterus, intrauterine gestational sac with or without an embryo Thick, irregular endometrial lining caused by residual trophoblastic tissue and fluid Embryo without cardiac activity; small size of the embryo for the gestational age (see Fig. 10)

Missed abortion

Complete abortion

Empty uterus

Inevitable abortion

Variable depending on the degree of bleeding and expulsion of the products of conception

Abbreviations: US, ultrasound.

to diagnose a failing pregnancy. TVUS features of failing pregnancy are summarized in Table 4. The sonographic findings are to be correlated with serum b-hCG and menstrual age. In the pre-embryonic stage, the pregnancy outcome depends on the presence of the gestational sac and yolk sac and their morphologic features. Absent intrauterine gestational sac Failure to demonstrate intrauterine gestational sac by TVUS may be secondary to early IUP (b-hCG < 1000 mIU/mL) or secondary to ectopic pregnancy. When the serum b-hCG is more than 1000 mIU/mL (IRP) and there is no IUP, an ectopic pregnancy [19,20] must be excluded by careful evaluation of the adnexa. If there is no identifiable ectopic gestational sac, adnexal mass, or a large amount of adnexal fluid in the cul-de-sac, follow-up with b-hCG and TVUS is necessary until a definite diagnosis is made. When the endometrial lining is thick with echoes in the endometrial cavity and no intrauterine gestational sacs, an incomplete abortion with retained products of conception must be distinguished from decidual reaction of ectopic gestation. Transvaginal color flow Doppler of the endometrial contents is useful in differentiating trophoblastic tissue from blood clots and pseudogestational sac. Sparse flow on color Doppler with low peak systolic velocities (< 6 cm/second) and low to absent end diastolic flow suggests decidual reaction of an ectopic pregnancy (Fig. 7) [38,39]. With early IUP (< 5 weeks) multiple flashes of color with a peak systolic velocity of greater than 8 cm/second

and high diastolic component caused by trophoblastic arterial flow are noted [40]. Intrauterine gestational sac without an embryo A common and difficult problem arises when the gestational sac in the uterus lacks an embryo or yolk sac [41 43]. This can be caused by early normal IUP,

Table 4 TVUS features of pregnancy failure Ultrasound findings Absence of IUGS with serum b-hCG above the discriminatory level (1000 mIU/mL) IUGS > 10 mm without a yolk sac IUGS of >18 mm without an embryo Embryo of 5 mm and above without cardiac activity Embryo with bradycardia (< 100 beats/min) Subchorionic hematoma Comments Ectopic pregnancy has to be excluded

Follow-up with serum b-hCG and TVUS Anembryonic pregnancy Embryonic demise Poor prognosis and needs close follow-up with TVUS Correlation of pregnancy outcome with the size of hematoma is not well established and needs TVUS follow-up

Abbreviations: hCG, human chorionic gonadotropin; IUGS, intrauterine gestational sac; TVUS, transvaginal ultrasound.

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Fig. 7. Decidual reaction. (A) Sagittal TVUS shows thick echogenic endometrial lining without a gestational sac (arrowheads). This sonographic appearance can be seen in molar pregnancy; correlation with beta hCG is very important. (B) Sagittal TVUS with color Doppler did not demonstrate trophoblastic flow, confirming it to be decidual reaction (arrowheads). Patients beta hCG was 650 IU. On follow-up, the patient was shown to have a normal intrauterine pregnancy.

anembryonic gestation, or a pseudogestational sac of ectopic pregnancy. Anembryonic gestation is a form of failed pregnancy defined as a gestational sac in which the embryo failed to develop (Fig. 8A). A mean gestational sac diameter greater than 18 mm (TVUS) without a visualized embryo is unequivocal evidence of a failed, anembryonic pregnancy [44]. This also is referred to as an empty amnion sign (Fig. 8B) because of its sonographic appearance of a large well-defined amniotic sac without an embryo [45]. The growth rate of an anembryonic gestational sac is slower than that of a normal gestational sac, which increases by 1.13 mm/day. An abnormal gestational sac can be identified confidently when the rate of increase of the mean sac diameter is less than

0.6 mm/d on follow-up US [46]. Other minor criteria of an abnormal gestational sac include distorted sac shape and weakly echogenic or irregular choriodecidual reaction (Fig. 9). The presence of gestational sac in the lower uterine segment or cervix is usually seen in patients with abortion in progress (Fig. 10), but can also be seen secondary to low implantation. Demonstration of trophoblastic vascular flow on color Doppler is useful in differentiating low implantation from abortion. Yolk sac criteria of an abnormal gestation The absence of a yolk sac when the mean sac diameter of the gestational sac is more than 10 mm is

Fig. 8. Anembryonic pregnancy. (A) TVUS of uterus shows a large (> 18 mm) gestational sac (arrow) without an embryo. (B) An empty amnion sign of anembryonic gestation (arrow).

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the viability of the gestation. The most convincing evidence that a pregnancy has failed is to document absence of cardiac activity when CRL length is greater than 5 mm. In a missed abortion, the embryo may be small for the gestational age with a discrepancy between the mean sac diameter and the CRL (Fig. 11). Embryonic bradycardia is a poor prognosticator of pregnancy viability and requires follow-up [58]. Embryonic bradycardia is defined as a heart rate of less than 100 beats per minute before 6.2 weeks gestational age and less than 120 beats per minute between 6.3 and 7 weeks [59].
Fig. 9. Abnormal shape of the gestational sac. A 30-year-old woman with 5 weeks of amenorrhea presents with vaginal spotting. A TVUS of the uterus shows an intrauterine gestational sac of abnormal shape and lobulated contour. On follow-up patient had a spontaneous complete abortion.

Intrauterine growth restriction First-trimester growth restriction is a sign of a failing pregnancy. Growth restriction is detected by comparing the mean sac diameter with the CRL or by serial follow-up of these growth parameters. The average gestational sac diameters should be at least 5 mm larger than the CRL. A difference in size between mean sac diameter and CRL of less than 5 mm caries a high risk of subsequent embryonic demise [60]. When there is sac size and CRL discrepancy, a follow-up US examination is recommended because these fetuses have higher incidence of low birth weight and premature delivery [61,62]. Subchorionic hematoma Up to 20% of women with a threatened abortion have a subchorionic hematoma [44]. Perigestational

indicative of an abnormal gestation and is associated with spontaneous abortion [47 49]. A failing or failed pregnancy is also suggested when the yolk sac is abnormal in size and shape. Large (> 6 mm) irregular and calcified yolk sacs have been found to correlate with early pregnancy failure [50 52]. A large yolk sac is considered to be caused by an alteration of the metabolic functions of the yolk sac membrane with accumulation of secretions following embryonic death [53]. The association of a large yolk sac with aneuploidy has also been reported [50]. Although abnormal large yolk sac size is reported to be associated with subsequent pregnancy failure, another study with yolk sac diameter greater than the 95th percentile for gestational age reported normal pregnancy outcomes [54]. Because of this controversial issue, any patient with a large yolk sac should have a follow-up US because there is increased risk of spontaneous abortion. Apart from size, irregular, echogenic, calcified, or double yolk sacs (vitelline duct cyst) also are associated with early pregnancy failure [55,56]. Gestational sac with an embryo Although visualization of a living embryo does not ensure a viable pregnancy, the abortion rate decreases for living embryos as the gestational age increases, with a 0.5% demise rate for living embryos between 6 and 10 mm [29]. Because cardiac activity may not be demonstrated [57] in early normal embryos (CRL < 4 mm), follow-up US and correlation with the serum b-hCG level is useful in determining

Fig. 10. Abortion in progress. A TVUS of the uterus shows a low-lying gestational sac (arrow). Mixed hyperechoic and hypoechoic contents in the endometrial cavity of the fundus (arrowheads) represent decidual reaction and hemorrhage. The patient had a complete spontaneous abortion a few hours after the scan.

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with that in younger women (13.8% versus 7.3%, respectively), and was 2.3 times higher in women who presented with vaginal bleeding at 8 weeks gestational age or less compared with that in women who presented with bleeding at more than 8 weeks gestational age (13.7% versus 5.9%, respectively). Some investigators have calculated the volume of a subchorionic hematoma as a percentage of the gestational sac volume. When the volume of a hematoma is less than 40% of the gestational sac volume, the pregnancy outcome is favorable [64,66].
Fig. 11. Missed abortion. A 35-year-old woman with 10 weeks of amenorrhea presents with intermittent vaginal bleeding. TVUS shows a relatively small-sized embryo (arrow) compared with the gestational sac. No cardiac activity was demonstrated on pulsed Doppler.

Retained products of conception Retained products of conception typically consist of retained placental tissue. An echogenic mass in the uterine cavity is the most suggestive US finding. A heterogeneous mass or collection in the central cavity may represent a blood clot, or some combination of retained placenta, necrotic debris, and clot (Fig. 13). Color Doppler may help to differentiate vascularized trophoblastic tissue from nonvascularized blood clots. A normal-appearing endometrial stripe or punctate echogenic foci not associated with a discrete mass makes retained products of conception unlikely.

hemorrhage from chorionic frondosum is the most common source of vaginal bleeding in the first trimester of pregnancy. Subchorionic hemorrhage is secondary to abruption of the edge of the chorion frondosum decidua basalis complex or may be caused by marginal sinus rupture [63,64]. Although the hemorrhage usually abuts or elevates the edge of the chorion frondosum decidua basalis complex, the bulk of the hemorrhage is usually situated between the decidua capsularis, chorion laeve, and the decidua vera. Acute hemorrhage may be hyperechoic or isoechoic relative to the chorion, and it becomes isoechoic with the chorionic fluid in 1 to 2 weeks (Fig. 12). Several studies have correlated the pregnancy outcome in these patients with the size of the subchorionic hematoma, gestational age, and the maternal age. One of the largest studies [65] showed that the rate of pregnancy loss increases with hematoma size, advancing maternal age, and earlier gestational age. In this study, the size of the hematoma was graded according to the percentage of the chorionic sac circumference elevated by the hematoma. It was graded as small when it involved less than one third of the chorionic sac circumference, moderate when it involved one-third to one-half of the chorionic sac circumference, and large when two-thirds or greater of the chorionic sac circumference was involved. There was little difference in the rates of spontaneous abortion between pregnancies with small- and moderate-size hematomas (7.7% and 9.2%, respectively), but the rate doubled with large hematomas (18.8%). The spontaneous abortion rate was also twice as high in women 35 years of age or older compared

Gestational trophoblastic disease Gestational trophoblastic disease is a spectrum of pregnancy-related trophoblastic proliferative abnormalities that can present with first-trimester bleeding.

Fig. 12. Subchorionic hemorrhage. TVUS shows a gestational sac (curved arrow), chorion (straight thick arrow), and a subchorionic hemorrhage (straight thin arrow).

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Fig. 13. Retained products of conception with variable appearance. Sagittal (A) and coronal (B) TVUS in two different patients with persistent vaginal bleeding after spontaneous abortion show retained products of conception with increased echogenicity (arrowheads) in (A) and heterogeneous appearance in (B). This appearance is secondary to necrosis and blood clots. (C) Increased vascularity on color flow Doppler evaluation in a patient with retained products of conception.

Classification of gestational trophoblastic disease is as follows: Hydatidiform mole Complete mole Partial mole Gestational trophoblastic tumors Choriocarcinoma Invasive mole Placental site trophoblastic tumor

Hydatidiform mole (molar pregnancy) Molar pregnancy is a noninvasive process characterized by varying degrees of trophoblastic prolif-

eration and edema of villous stroma. Its incidence is 1 in every 1000 to 2000 pregnancies [67] and is estimated to be as high as 1 in 41 in patients with miscarriages [68]. Hydatidiform mole constitutes 80% of the cases of gestational trophoblastic disease with relatively high frequency of molar pregnancy at the beginning and end of the childbearing period. Mole recurrence is seen in about 1% to 2% of cases [69]. The absence or presence of fetus or embryonic elements is used to classify a molar pregnancy into complete or partial moles. Complete molar pregnancies are most often 46 XX, with the chromosomes completely of paternal origin and are referred to as androgenesis. The karyotype in partial mole is usually triploid (69 XXY) or even tetraploid (92 XXXY) with one maternal and two paternal haploid compo-

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nents. The fetus in partial mole is usually nonviable and exhibits features of triploidy, which include multiple congenital anomalies and growth restriction [70]. Histologically, the molar tissue has prominent villi with central acellular space corresponding to the macroscopic appearance of vesicles. In partial mole these changes are focal and less advanced. The clinical presentation of molar pregnancy, listed below, has changed appreciably over the last decades because of early diagnosis with TVUS and quantitative b-hCG estimation.
 Uterine bleeding, which may vary from spotting

agnosis is made by markedly elevated serum b-hCG levels expected for the stage of gestation and by the characteristic sonographic appearance. Sonographic features of molar pregnancy Molar changes can be detected from 8 weeks of pregnancy by US. The uterine cavity is filled with multiple sonolucent areas of varying size and shape. This has been described as a snow storm appearance with low-frequency transabdominal scanning. With high-frequency transvaginal transducers, numerous discrete, anechoic (cystic) spaces are visualized corresponding to the hydropic villi (Fig. 14). These cystic spaces range from 1 to 30 mm in size and increase in size with gestational age. Large sonolucent areas or maternal lakes resulting from the stasis of maternal blood are seen between the vesicles. In partial mole, an intrauterine embryo is noted along with molar changes [71,72]. Because the trophoblastic changes develop at a slower rate in partial mole, it may present as enlarged placenta without macroscopic vesicular changes [73]. Women with a high b-hCG level for the gestational age without sonographic molar changes should have follow-up US to exclude partial mole. In missed abortion, impaired trophoblastic vascularity leads to hydropic degeneration of villi and can resemble a partial hydatidiform mole on US. The serum b-hCG is not elevated, however, and may be normal or at a lower level than for

to profuse hemorrhage
 Uterine enlargement out of proportion to the

duration of pregnancy in 50% of cases


 Absence of fetal parts or fetal heart sounds

despite an enlarged uterus


 Pregnancy-induced hypertension before

24 weeks gestation
 Hyperemesis  Thyrotoxicosis, which is usually subclinical  History of passage of grape-like vesicles trans-

vaginally Uterine bleeding is the most common presentation and it may vary from spotting to profuse bleeding. Occasionally patients may pass grape-like vesicles transvaginally. Clinically the uterine fundal height is more than is expected for the gestational period. Di-

Fig. 14. Complete hydatidiform mole. (A) Transabdominal sonogram of the uterus shows a complex mass with multiple welldefined anechoic cystic areas (arrows) corresponding to the vesicles of hydatidiform mole. There was no associated embryo. (B) Corresponding T1-weighted postgadolinium image of the uterus demonstrates intrauterine complex mass (arrowheads) with multiple well-defined hypointense lesions that are not enhancing and represent vesicles of hydatidiform mole (arrow).

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the expected gestational age. Rarely, a viable fetus may be associated with complete molar pregnancy [74] and is caused by the coexistence of a true mole and a normal fetus in dizygotic twin gestation. Demonstration of the typical trophoblastic flow is useful in differentiating the trophoblastic tissue of molar pregnancy from intrauterine blood clots in a patient with abortion. Theca-leutin ovarian cysts are seen in up to 25% to 60% of cases because of hyperstimulation of the ovaries by chorionic gonadotrophin secreted by the trophoblastic tissue [75]. In this condition, the ovaries are enlarged with multiple cysts having a soap bubble or spoke-wheel appearance. Treatment of hydatidiform mole consists of immediate evacuation of the mole and subsequent follow-up with serial measurement of serum b-hCG for detection of persistent trophoblastic proliferation or malignant change. TVUS is useful in monitoring patients following evacuation and chemotherapy [76 79]. If the b-hCG levels plateau or continue to rise, persistent trophoblastic tissue is diagnosed. Following evacuation of a hydatidiform mole, 18% to 29% with complete hydatidiform mole and 1% to 11% with partial mole develop a persistent trophoblastic tumor [80 83]. TVUS reveals nodules of residual echogenic trophoblastic tissue and central hypoechoic blood spaces. Doppler interrogation reveals typical low-resistance and high-peak systolic velocity vascular flow of trophoblastic tissue. Gestational trophoblastic tumors Gestational trophoblastic tumor refers to choriocarcinoma, invasive mole, and placental site trophoblastic tumor. It may follow a normal or a molar pregnancy, abortion, or ectopic pregnancy. Diagnosis is made primarily by persistent elevation of the serum b-hCG. Fifty percent of these tumors arise following hydatidiform mole, 25% following abortion, and 25% following normal or ectopic pregnancy [84]. Choriocarcinoma Choriocarcinoma is a malignant form of trophoblastic tumor that invades uterine myometrium and blood vessels resulting in distant metastasis. The absence of villous pattern is characteristic of choriocarcinoma, in contrast to hydatidiform mole and invasive mole. The most common sites of metastases are the lungs (over 75%) and the vagina (50%). Other sites of metastases include the vulva, liver, kidneys, brain, ovaries, and bowel [85]. The US appearance is indistinguishable from a complete mole, except in cases with myometrial and parametrial extension. TVUS reveals a heterogeneous intrauterine mass with

or without myometrial invasion. Doppler interrogation reveals typical trophoblastic flow and differentiates trophoblastic tissue from areas of hemorrhage and necrosis. Ovarian theca-leutin cysts are identified in more than a third of such cases. Cross-sectional imaging with CT and MR imaging is more accurate in demonstrating invasion of the myometrium and parametrium. Radiologic evaluation for distant metastases is mandatory in all cases of choriocarcinoma. Invasive mole This is defined as excessive trophoblastic overgrowth with invasion of the myometrium and occasional extension to the peritoneum or adjacent parametrium. Unlike choriocarcinoma there are no distant metastases. Invasive mole presents clinically as heavy vaginal bleeding after the evacuation of the molar pregnancy with persistent elevation of serum b-hCG. On TVUS it appears as focal areas of increased echogenicity within the myometrium [86]. Doppler color flow mapping of this area can evaluate the extent of this lesion and its subsequent response to chemotherapy (Fig. 15) [87 89]. Placental site trophoblastic tumor This is a very rare trophoblastic tumor, which arises from the placental implantation site following either a normal term pregnancy or abortion. These patients present with either abnormal bleeding or amenorrhea and might be presumed to be pregnant. Moreover, the b-hCG levels are not as high as in other forms of gestational trophoblastic disease [90,91]. They may invade the myometrium and in 15% to 20% cases behave in a malignant fashion with distant metastases. US features are indistinguishable from those of other gestational trophoblastic tumors [92,93].

Arteriovenous malformation of the uterus It is important to consider arteriovenous malformations in the differential diagnosis of first-trimester bleeding because of their sonographic resemblance to retained products of conception and gestational trophoblastic disease. Vascular malformations of the uterus are rare and potentially life-threatening lesions. They can be congenital or acquired following uterine trauma (surgery or curettage); use of intrauterine contraceptive devices; endometrial or cervical carcinoma; and previous treatment of gestational trophoblastic tumors [94]. Congenital arteriovenous malformations have multiple arteriovenous communications and may extend through the myometrium into the parametrium. Acquired lesions are arterio-

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Fig. 15. Invasive mole. (A) TVUS showing molar tissue invading the myometrial wall (arrowheads) of the fundus and endometrial cavity (arrow). (B) Color flow Doppler evaluation shows vascularity of the invaded myometrium. Endometrial cavity is shown by arrow. (C) Corresponding T2-weighted, sagittal image of the uterus demonstrates hyperintense myometrium (arrow) representing invasive molar tissue. Uninvolved endometrial lining is shown (arrowheads).

venous fistulas between a single artery and a vein. Vascular malformations persist following treatment in 10% to 15% of patients with gestational trophoblastic tumors. Gray-scale US shows multiple anechoic spaces with mosaic pattern of color signals within the cystic spaces on color Doppler US. Spectral analysis of the vessels shows high-velocity blood flow with a low resistive index [95,96], indistinguishable from a gestational trophoblastic disease (Fig. 16). These vessels can be distinguished from gestational trophoblastic disease because the serum b-hCG is normal.

Uterine arteriovenous malformations are one of the common causes of spontaneous abortions. Contrastenhanced CT, MR imaging, and angiography are other imaging modalities used to diagnose uterine arteriovenous malformations. The diagnosis of uterine arteriovenous malformations as the cause of vaginal bleeding is crucial because treatment is entirely different from that for retained products of conception or gestational trophoblastic disease, which can mimic arteriovenous malformations. The treatment of arteriovenous malformations is by embolization if the

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Fig. 16. Uterine arteriovenous malformation in a 35-year-old woman with history of spontaneous abortion presenting with vaginal bleeding. She was referred to exclude retained products of conception. (A) TVUS shows complex endometrial mass (arrowheads) with anechoic spaces (arrow). (B) Corresponding color flow Doppler demonstrates the mosaic pattern of flow within the mass (arrowheads). Arrow points to endometrial cavity. Pulsed Doppler (C) shows arterialized venous flow, diagnostic of arteriovenous malformation.

patient desires fertility and by hysterectomy if fertility is not an issue.

of early pregnancy failure can be made even before the embryo is visible.

Summary Vaginal bleeding is a leading cause of presentation for emergency care during the first trimester of the pregnancy. Clinical assessment of the pregnancy outcome at this stage is less reliable. US examination is crucial in establishing IUP and early pregnancy failure and to exclude other causes of bleeding, such as ectopic pregnancy and molar pregnancy. Diagnosis of a normal IUP at this stage not only assists the physician in an expectant management, but also gives a psychologic boost to the patient. With recent advances in US technology and the availability of highfrequency transvaginal transducers, reliable diagnosis

Acknowledgment The authors thank Bonnie Hami, MA, Department of Radiology, University Hospitals of Cleveland, Ohio, for her editorial assistance in the preparation of this article.

References
[1] Nyberg DA, Laing FC, Filly RA. Threatened abortion: sonographic distribution of normal and abnormal gestation sacs. Radiology 1986;158:397 400.

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R.M. Paspulati et al / Radiol Clin N Am 42 (2004) 297314 of early intrauterine pregnancy: use in exclusion of ectopic pregnancy. Radiology 1982;143:223 6. Nyberg DA, Filly RA, Duarte DL, et al. Abnormal pregnancy: early diagnosis by US and serum chorionic gonadotropin levels. Radiology 1986;158:393 6. Kadar N, Devore G, Romero R. Discriminatory hCG zone: its use in the sonographic evaluation for ectopic pregnancy. Obstet Gynecol 1981;58:156. Moore KL. Formation of bilaminar embryo. In: Wonsiewicz M, editor. The developing embryo. 4th edition. Philadelphia: WB Saunders; 1988. p. 38 49. Levi CS, Lyons EA, Lindsay DJ. Early diagnosis of non viable pregnancy with transvaginal US. Radiology 1988;167:383 5. Moore KL. The placenta and fetal membrane. In: Moore KL, editor. The developing human embryo: clinically oriented embryology. 4th edition. Philadelphia: WB Saunders; 1988. p. 121. Gitlin D, Pericelli A. Synthesis of serum albumin, prealbumin, alpha 1-antitrypsin and transferin by the human yolk sac. Nature 1970;228:995. Jauniaux E, Jurkovic D, Henreity Y, et al. Development of the secondary human yolk sac: correlation of sonographic and anatomical features. Hum Reprod 1991;6: 1160 6. Yeh HC, Rabinowitz JG. Letter. J Ultrasound Med 1995;14:97 9. Goldstein SR, Wolfson R. Transvaginal ultrasonographic measurement of early embryonic size as a means of assessing gestational age. J Ultrasound Med 1994;13:27 31. Daya S. Accuracy of gestational age estimation by means of the fetal crown-rump length measurement. Am J Obstet Gynecol 1993;168:903 8. Wisser J, Dirschedl P, Krone S. Estimation of gestational age by transvaginal sonographic measurement of the greatest embryonic length in dated human embryos. Ultrasound Obstet Gynecol 1994;4:457 62. Levi CS, Lyons EA, Zheng XH, et al. Transvaginal US: demonstration of cardiac activity in embryos of less than 5.0 mm in crown rump length. Radiology 1990; 176:71 4. Brown DL, Emerson DS, Fleker RF, et al. Diagnosis of early embryonic demise by transvaginal sonography. J Ultrasound Med 1990;9:631 6. Pennell RG, Needleman L, Pajak T, et al. Prospective comparison of vaginal and abdominal sonography in normal early pregnancy. J Ultrasound Med 1991;10: 63 7. Goldstein SR. Embryonic death in early pregnancy: a new look at the first trimester. Obstet Gynecol 1994; 84:294 7. Hertzberg BS, Mahony BS, Bowie JD. First trimester fetal cardiac activity: sonographic documentation of a progressive early rise in heart rate. J Ultrasound Med 1988;7:573 5. Achiron R, Tadmor O, Machiac S. Heart rate as a predictor of first-trimester spontaneous abortion after

[2] Laing FC, Brown DL, DiSalvo DN. Gynecologic ultrasound. Radiol Clin North Am 2001;39:523 40. [3] Goldstein RB, Bree RL, Benson CB, Benacerraf BR, Bloss JD, Carlos R, et al. Evaluation of the woman with postmenopausal bleeding: Society of Radiologists in Ultrasound-Sponsored Consensus Conference statement. J Ultrasound Med 2001;20:1025 36. [4] Forrest TS, Elyaderani MK, Mulenberg MI, et al. Cyclic endometrial changes: US assessment with histologic correlation. Radiology 1988;167:233 7. [5] Tamarkin S, Dogra V. Benign and malignant adnexal lesions. In: Dogra V, Rubens D, editors. Ultrasound secrets. Philadelphia: Hanley & Belfus; 2004. p. 97 104. [6] Kremkeu FW. Performance and safety. In: Kremkau FW, editor. Diagnostic ultrasound: principles and instruments. 4th edition. Philadelphia: WB Saunders; 1993. p. 286. [7] Implementation of the principle of as low as reasonably achievable (ALARA) for medical and dental personnel. NRCP report 107. Bethesda, MD: National Council on Radiation Protection and Measurements; 1990. [8] Nyberg DA, Hill LM. Normal early intrauterine pregnancy: sonographic development and HCG correlation. In: Patterson AS, editor. Transvaginal ultrasound. St. Louis: Mosby; 1992. p. 64 85. [9] Yeh HC, Rabinowitz JG. Amniotic sac development: ultrasound features of early pregnancy: The bouble bleb sign. Radiology 1988;166:97 103. [10] Moore KL. Formation of the bilaminar embryo: the second week. In: Keith L, editor. The developing human: clinically oriented embryology. 5th edition. Philadelphia: WB Saunders; 1988. p. 38. [11] Emerson DS, Cartier MS, Altieri LA, et al. Diagnostic efficacy of endovaginal color flow imaging in an ectopic pregnancy scanning program. Radiology 1992; 183:413 20. [12] Dillon EH, Feyock AL, Taylor KJ. Pseudogestational sacs: Doppler US differentiation from normal or abnormal intrauterine pregnancies. Radiology 1990;176: 359 64. [13] Yeh HC, Goodman JD, Carr L, Rabinowitz JG. Intradecidual sign: a US criterion of early intrauterine pregnancy. Radiology 1986;161:463 7. [14] Laing FC, Brown DL, Price JF, et al. Intradecidual sign: Is it effective in diagnosis of an early intrauterine pregnancy? Radiology 1997;204:655 60. [15] Trimor-Tritsch IE, Farine D, Rosen MG. A close look at early embryonic development with the high frequency transvaginal transducer. Am J Obstet Gynecol 1988; 159:676 81. [16] Rosavic IK, Torjusen GO, Gibbons WE. Conceptual age and ultrasound measurements of gestational sac and crown-rump length in vitro fertilization pregnancies. Fertil Steril 1988;49:1012 7. [17] de crespigny LC, Cooper D, Mckenna M. Early detection of intrauterine pregnancy with ultrasound. J Ultrasound Med 1988;7:7 10. [18] Bradley WG, Fiske CE, Filly RA. The double sac sign

[19]

[20]

[21]

[22]

[23]

[24]

[25]

[26] [27]

[28]

[29]

[30]

[31]

[32]

[33]

[34]

[35]

R.M. Paspulati et al / Radiol Clin N Am 42 (2004) 297314 ultrasound proven viability. Obstet Gynecol 1991;78: 330 3. May DA, Sturtevant NV. Embryonal heart rate as a predictor of pregnancy out come: a prospective analysis. J Ultrasound 1991;10:591 3. Fleischer AC, James AE, Dawes WJ, Paige M, Robinson HP. Sonographic depiction of pregnancy during embryonic development. In: Sanders RC, James AE, editors. The principles and practice of ultrasonography in obstetrics and gynaecology. 3rd edition. Norwalk (CT): Appleton-Century- Crofts; 1985. p. 61 74. Jaffe R, Dorgan A, Abramowicz JS. Color Doppler imaging of the uteroplacental circulation in the first trimester: value in predicting pregnancy failure or complication. AJR Am J Roentgenol 1995;164:1255 8. Emerson DS, Cartier MS, Altieri LA, et al. Diagnostic efficacy of transvaginal color Doppler flow imaging in an ectopic pregnancy program. Radiology 1992;183: 413 20. Parvey HR, Dubinsky TJ, Johnston DA, Maklad NF. The chorionic rim and low-impedance intrauterine arterial flow in the diagnosis of early intrauterine pregnancy: evaluation of efficacy. AJR Am J Roentgenol 1996;167:1479 85. Robinson HP. The diagnosis of early pregnancy failure by sonar. Br J Obstet Gynaecol 1975;82:849 57. Donald I, Mosley P, Barnett E. The diagnosis of the blighted ovum by sonar. Br J Obstet Gynaecol 1972; 79:304 10. Jouppila P, Hesva T. Study of blighted ovum by ultrasonic and histopathology methods. Obstet Gynecol 1980;55:574 8. Nyberg DA, Laing FC. Threatened abortion and abnormal first trimester intrauterine pregnancy. In: Patterson AS, editor. Transvaginal ultrasound. St Louis: Mosby; 1992. p. 85 103. McKenna KM, Feldstein VA, Goldstein RB, Filly RA. The empty amnion: a sign of early pregnancy failure. J Ultrasound Med 1995;14:117 21. Bromley B, Harlow BL, et al. Small sac size in the first trimester: a predictor of poor fetal out come. Radiology 1991;178:375 7. Levi CS, Lyons EA, Lindsay DJ. Early diagnosis of non viable pregnancy with endovaginal US. Radiology 1988;167:383. Crooij MJ, Westhuis J, Schoemaker J, et al. Ultrasonographic measurement of the yolk sac. Br J Obstet Gynecol 1982;89:931 4. Green JJ, Hobbins JC. Abdominal ultrasound examination of the first-trimester fetus. Am J Obstet Gynecol 1988;159:165 75. Lindsay DJ, Lovett IS, Lyons EA, et al. Yolk sac diameter and shape at endovaginal US: predictors of pregnancy outcome in the first trimester. Radiology 1992;183:115 8. Stampone C, Nicotra M, Muttinelli C, et al. Transvaginal sonography of the yolk sac in normal and abnormal pregnancy. J Clin Ultrasound 1996;24:3 9. Dugoff L, Persutte WH, Schultz L, Hobbins JC. Prog-

313

[36]

[53]

[37]

[54]

[55]

[38]

[56]

[39]

[57]

[40]

[58]

[59]

[41] [42]

[60]

[61]

[43]

[44]

[62]

[45]

[63]

[46]

[64]

[47]

[65]

[48]

[66]

[49]

[50]

[67]

[51]

[68]

[52]

[69]

nostic significance of the large yolk sac. Am J Obstet Gynaecol 1998;178:S165. Ferrazi E, Brambati B, Lauzani A, et al. The yolk sac in early pregnancy failure. Am J Obstet Gynaecol 1988;158:137. Stampone C, Nicotra M, Muttinelli C, Cosmi EV. Transvaginal sonography of the yolk sac in normal and abnormal pregnancy. J Clin Ultrasound 1996;24: 3 9. Harris RD, Vincent LM, Askin FB. Yolk sac calcification: a sonographic finding associated with intrauterine embryonic demise in the first trimester. Radiology 1988;166:109 10. Barzilai M, Lyons EA, Levi CS, Lindsay DJ. Vitelline duct cyst or double yolk sac. J Ultrasound Med 1989;8: 523 6. Brown DL, Emerson DS, Felker RE, et al. Diagnosis of early embryonic demise by endovaginal sonography. J Ultrasound Med 1990;9:631 6. Benson CB, Doubilet PM. Slow embryonic heart rate in early first trimester: indicator of poor pregnancy out come. Radiology 1994;192:343 4. Doubilet PM, Benson CB. Embryonic heart rate in the early first trimester: What rate is normal? J Ultrasound Med 1995;14:431 4. Bromley B, Harlow BL, Laboda LA, et al. Small sac size in the first trimester: a predictor of poor fetal out come. Radiology 1991;178:375 7. Dickey RP, Gasser RF. Ultrasound evidence for variability in the size and development of normal human embryos before the tenth post insemination week after assisted reproductive technologies. Hum Reprod 1993; 8:331 7. Smith GS, Smith MF, McNay MB, Flemming JEE. First trimester growth and the risk of low birth weight. N Engl J Med 1998;339:1817 22. Nyberg DA, Cyr DR, Mack LA, et al. Sonographic spectrum of placental abruption. AJR Am J Roentgenol 1987;148:161. Sauerbrei EE, Pham DH. Placental abruption and sub chorionic haemorrhage in the first half of pregnancy: US appearance and clinical out come. Radiology 1986; 160:109 12. Bennett GL, Bromley B, Lieberman E, Benacerraf BR. Subchorionic hemorrhage in first trimester pregnancies: prediction of pregnancy outcome with sonography. Radiology 1996;200:803 6. Stabile I, Campbell S, Grudzinskas JG. Threatened miscarriage and intrauterine hematomas: sonographic and biochemical studies. J Ultrasound Med 1989; 8:289. Contran RS, Kumar V, Robbins SL. Female genital tract. In: Contran RS, Kumar V, Robbins SL, editors. Robbins pathologic basis of disease. 4th edition. Philadelphia: WB Saunders; 1989. p. 1174 8. Jeffers MD, ODwyer P, Curran B, et al. Partial hydatidiform mole: a common but under diagnosed condition. Int J Gynecol Pathol 1993;12:315. Miller DS, Ballon SC, Teng NNH. Gestational tropho-

314

R.M. Paspulati et al / Radiol Clin N Am 42 (2004) 297314 blastic diseases. In: Broody SA, Veland K, editors. Endocrine disorders in pregnancy. Norwalk (CT): Appleton & Lange; 1989. p. 451. Lawler SD, Fisher RA, Dent J. A prospective genetic study of complete and partial hydatidiform moles. Am J Obstet Gynecol 1991;164:1270 7. Szulman AE, Surti U. The syndromes of hydatidiform mole: I. Cytogenetic and morphologic correlations. Am J Obstet Gynecol 1978;131:665. Szulman AE, Surti U. The syndromes of hydatidiform mole: II. Morphologic evolution of the complete and partial mole. Am J Obstet Gynecol 1978;132:22. Fine C, Bundy AL, Berkowitz RS, et al. Sonographic diagnosis of partial hydatidiform mole. Obstet Gynecol 1989;73:414. Steller MA, Genest DR, Bernstein MR, et al. Natural history of twin pregnancy with complete hydatidiform mole and coexisting fetus. Obstet Gynecol 1994; 83:35. Green CL, Angtuaco TL, Shah HR, Parmley TH. Gestational trophoblastic disease: a spectrum of radiologic diagnosis. Radiographics 1996;16:1371 84. Tepper R, Shulman A, Altaras M, et al. The role of color Doppler flow in the management of nonmetatstatic gestational trophoblastic disease. Gynecol Obstet Invest 1994;38:14. Mayman R, Schneider D, Schulman A, et al. Serial color Doppler flow of uterine vasculature combined with serum beta-hCG measurements for improved monitoring of patients with gestational trophoblastic disease. Gynecol Obstet Invest 1996;42:201. Zanetta G, Lissoni A, Colombo M, et al. Detection of abnormal intrauterine vascularization by color Doppler imaging: a possible additional aid for the follow up of patients with gestational trophoblastic tumors. Ultrasound Obstet Gynecol 1996;7:32. Long MG, Boultbee JE, Begent RH, et al. Preliminary Doppler studies on the uterine artery and myometrium in trophoblastic tumors requiring chemotherapy. Br J Obstet Gynaecol 1990;97:686. Jauniaux E, Gulbis B, Hyett J, et al. Biochemical analysis of mesenchymal fluid in early pregnancy. Am J Obstet Gynecol 1998;178:765. Berkowitz RS, Goldstein DP. Chorionic tumors. N Engl J Med 1996;335:1740. Bagshave KD, Lawler SD, Paradinas FJ, et al. Gestational trophoblastic tumors following initial diagnosis of partial hydatidiform mole. Lancet 1990;335:1074. Chen RJ, Huang SC, Chow SN, et al. Persistent gestational trophoblastic tumour with partial hydatidiform mole as the antecedent pregnancy. Br J Obstet Gynaecol 1994;101:330. Cunningham FG, MacDonald PC, Grant NF, Leveno KJ, Gilstrap LC. Diseases and abnormalities of the placenta. In: Licht J, editor. Williams obstetrics. 19th edition. Norwalk (CT): Appleton & Lange; 1993. p. 748 59. Fine C, Bundy AL, Berkowitz RS, et al. Sonographic diagnosis of partial hydatidiform mole. Obstet Gynecol 1989;73:414. Aoki S, Hata T, Hata K, et al. Doppler color flow mapping of an invasive mole. Gynecol Obstet Invest 1989;27:52. Desai RK, Desberg AL. Diagnosis of gestational trophoblastic disease: value of endovaginal color flow Doppler sonography. AJR Am J Roentgenol 1991;157:787. Chau MT, Chan FY, Pun TC, et al. Perforation of the uterus by an invasive mole using color Doppler ultrasound: case report. Ultrasound Obstet Gynecol 1993; 3:51. Bagshawe KD. Choriocarcinoma: a model for tumour markers. Acta Oncol 1992;31:99 106. Mazur MT, Kurman RJ. Gestational trophoblastic disease and related lesions. In: Kurman RJ, editor. Blausteins pathology of the female genital tract. New York: Springer Verlag; 1994. p. 1049 92. Caspi B, Elchalal U, Dgani R, Ben-Hur H, Rozenman D, Nissim F. Invasive mole and placental site trophoblastic tumor: two entities of gestational trophoblastic disease with a common ultrasonographic appearance. J Ultrasound Med 1991;10:517 9. Abulafia O, Sherer DM, Fultz PJ, Sternberg LB, Angel C. Unusual endovaginal ultrasonography and magnetic resonance imaging of placental site trophoblastic tumor. Am J Obstet Gynecol 1993;170:750 2. Newlands ES, Barghawe KD, Begent HJ, Rustin GJS, Holden L, Dent J. Developments in chemotherapy for medium and high risk patients with gestational trophoblastic tumors. Br J Obstet Gynaecol 1986;93:63 9. Abu Musa A, Hata T, Hata K, Kitao M. Pelvic arteriovenous malformation diagnosed by color flow Doppler imaging. AJR Am J Roentgenol 1989;152:1311 2. Sugiyama T. Diagnosis of uterine arterivenous malformation by color and pulsed Doppler ultrasonography. Ultrasound Obstet Gynecol 1996;8:359 60. Pelage JP, Soyer P, Repiquet D, et al. Secondary post partum hemorrhage: treatment with selective arterial embolization. Radiology 1999;212:385 9.

[70]

[84]

[71]

[85]

[72]

[86]

[73]

[87]

[74]

[88]

[75]

[89] [90]

[76]

[77]

[91]

[78]

[92]

[79]

[93]

[80]

[94]

[81] [82]

[95]

[96]

[83]

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