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Subsequent chapters will discuss the technique and clinical use of colour Doppler and power Doppler measurements.
Preliminary results raise the possibility of detecting increased vascularity and new vessel formation in cases of malignant ovarian masses. In general, vessels in malignant tumours lack the muscle layer and have lower impedance. However, increased flow may also be seen with pelvic inflammatory processes. The pres­ence of a corpus luteum not only may be misleading in the structural evaluation of an adnexal mass since the flow measurement values overlap with those found in ovarian cancer. The corpus luteum is known to have new vessel formation, which lowers the resistance to flow while present.
Recent studies have suggested a possible role for colour Doppler in the diag­nosis of adnexal torsion.
15,23
These studies suggest that, at the site of the torsion, the diameter of the vessels proximal to the occlusion is increased; the disruption of flow is identified on colour Doppler. Within the twisted adnexa, there is sig­nificantly diminished flow or no flow at all. The cost–benefit ratio of colour flow studies is still under investigation, and the value of such studies is as yet not fully determined. Moreover, the technique requires a great deal of training, and mea­surement remains a subjective process.

SCREENING FOR OVARIAN MASSES

Scanning techniques in obstetrics and gynaecology
Transvaginal sonography, with or without colour flow-directed measurements of resistance to flow and flow velocities, has been suggested as a means of screen­ing for ovarian cancer.
5,7,24
Although transvaginal sonography is probably the best means of determining the morphological structure of adnexal masses, its effi­cacy in screening for ovarian cancer has not been adequately established. Both modalities – transvaginal sonography and colour flow-directed measurements – are experimental for these uses.
11,49,59
Several studies are under way to determine whether transvaginal sonography and colour Doppler in conjunction with biological markers (proteins) can be used to screen a selected population at high risk for ovarian cancer. Other stud­ies are being done to examine the feasibility of using transvaginal sonography as a first-line modality for screening. Doubts about the value of colour Doppler in the diagnosis of ovarian masses have also been expressed.
45-47

TRANSPERINEAL AND TRANSRECTAL SCANNING

This chapter would not be complete without mentioning other scanning routes. The transperineal route is also called translabial scanning. It is mainly used if transvaginal scanning is not possible (no transvaginal transducer is available or a contraindication prevents its use). transducer is inserted in a glove and applied to the vulvar area in a sagittal fashion.
The authors' experience is that there are very few contradictions to the use of transvaginal probes in favour of a transperineal scan. Even in the case of premature
21,41
A linear or curvilinear
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rupture of the membranes, it was found that one transvaginal scan can be more useful than one digital examination to predict premature delivery.
19,37
In cases where transvaginal scanning is not feasible or is contradicted, transrec-
tal scanning can be used.
55

ULTRASOUND-GUIDED PUNCTURE PROCEDURES

There are two kinds of ultrasound-guided puncture procedures: those guided by a transabdominal transducer and performed transabdominally and those guided by a transvaginal transducer and performed transvaginally.
Transabdominal puncture procedures can be done using the ‘free hand’ method or a fixed needle guide. The former requires some degree of experience and good eye–hand co-ordination.
Transvaginal puncture procedures should always be performed using a fixed needle guide which is ‘mated’ to the shaft of the transvaginal probe.
Ultrasound in obstetrics and gynaecology

CONCLUSION

The technique and clinical aspects of transabdominal and transvaginal ultrasound have been discussed. Those who intend to perform hands-on scanning of obstet­ric and gynaecological patients should familiarize themselves with the described techniques. In addition, the more specific and detailed texts and published articles should be read.
Based upon our experience, the evolution of understanding in this imaging specialty is closely related to advances in the fields of electronics, acoustics and computer sciences as well as to the ability to miniaturize most components of the ultrasound equipment.
54

References

1. American College of Obstetricians and
Gynecologists 1993 ACOG technical bulletin no. 187. American College of Obstetricians and Gynecologists, Washington, DC
2. American College of Obstetricians and
Gynecologists 1995 ACOG technical bulletin no. 215. American College of Obstetricians and Gynecologists, Washington, DC
3. Benacerraf BR, Ship TD, Bromley
B. Is a full bladder still necessary for pelvic sonography? J Ultrasound Med 2000;19:237–241
4. Bernaschek G, Deutinger J. Current status
of vaginosonography – a world-wide inquiry. Ultrasound Obstet Gynecol 1992;2:352–356
5. Bourne TH, Hampson J, Reynolds K, Collins
WP, Campbell S. Screening for early ovarian cancer. Br J Hosp Med 1992;48:454–459
6. Callen PW. Ultrasonography in obstetrics and gynecology, 4th edn. WB Saunders, Philadelphia, 2000
7. Campbell S, Bourne T, Bradley E. Screening for ovarian cancer by transvaginal sonography and colour Doppler. Eur J Obstet Gynecol Reprod Biol 1993;49:33–34
8. Chervenak FA, Isaacson GC, Campbell S. Ultrasound in obstetrics and gynecology. Little, Brown, Boston, 1993
9. Cicero S, Sacchini C, Rembouskos G, Nicolaides KH. Sonographic markers of fetal aneuploidy – a review. Placenta 2003;24 (suppl B):S88–98
10. Coleman BG, Arger PH, Grumbach K et al. TVS and TAS sonography: prospective comparison. Radiology 1988;168:639–643
11. Daskalakis G, Kalmantis K, Skartados N et al. Assessment of ovarian tumors using
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transvaginal color Doppler ultrasonography. Eur J Gynaecol Oncol 2004;25:594–596
12. Dodson MG, Deter RL. Definition of anatomical planes for use in transvaginal sonography. J Clin Ultrasound 1990;18: 239–242
13. Economides DL, Whitlow BJ, Braithwaite JM. Ultrasonography in the detection of fetal anomalies in early pregnancy. Br J Obstet Gynaecol 1999;106:516–523
14. Fleischer AC, Romero R, Manning FA et al. The principle and the practice of ultrasonography in obstetrics and gynecology, 5th edn. Appleton and Lange, Stamford, CT, 1996
15. Fleischer AC, Stein SM, Cullinan JA, Warner MA. Color Doppler sonography of adnexal torsion. J Ultrasound Med 1995;14:523–528
16. Goldstein SR, Timor-Tritsch IE (eds). Ultrasound in gynecology. Churchill Livingstone, New York, 1995
17. Goldstein SR. Endovaginal sonography, 2nd edn. Wiley-Liss, New York, 1991
18. Goldstein SR. Use of ultrasonohysterography for triage of perimenopausal patients with unexplained uterine bleed. Am J Obstet Gynecol 1994;170:565–570
19. Gomez R, Galasso M, Romero R et al. Ultrasonographic examination of the uterine cervix is better than cervical digital examination as a predictor of the likelihood of premature delivery in patients with preterm labor and intact membranes. Am J Obstet Gynecol 1994;171(4):956–964
20. Hendrick WR, Hykes DL, Starchman DE. Ultrasound physics and instrumentation, 3rd edn. Mosby, St Louis, MO, 1995
21. Hertzberg BS, Bowie JD, Weber TM, Carroll BA, Kliewer MA, Jordan SG. Sonography of the cervix during the third trimester of pregnancy: value of the transperineal approach. Am J Roentgenol 1991;157: 73–76
22. Kossoff G, Griffith KA, Dixon CE. Is the quality of transvaginal images superior to transabdominal ones under matched conditions? Ultrasound Obstet Gynecol 1991;1:29–35
23. Kupesic S, Aksamija A, Vucic N, Tripalo A, Kurjak A. Ultrasonography in acute pelvic pain. Acta Med Croatica 2002;56:171–180
24. Kurjak A, Shalan H, Matijevic R, Predanic M, Kupesic-Urek S. Stage I ovarian cancer by transvaginal color Doppler sonography: a report of 18 cases. Ultrasound Obstet Gynecol 1993;3:195–198
25. Lavery MJ, Benson CB. Transvaginal versus transabdominal ultrasound. In: Timor­Tritsch IE, Rottem S (eds) Transvaginal sonography, 2nd edn. Chapman and Hall, New York, 1991
26. Manning FA, Harman CR, Morrison I, Menticoglou SM, Lange IR, Johnson JM. Fetal assessment based on fetal biophysical profile scoring. IV. An analysis of perinatal morbidity and mortality. Am J Obstet Gynecol 1990;162:703–709
27. Mendelson EB, Bohm-Velez M, Joseph N, Neiman HL. Gynecologic imaging: comparison of TAS and TVS sonography. Radiology 1988;166:321–324
28. Merz E. Three-dimensional ultrasound in obstetrics and gynecology. Lippincott Williams and Wilkins, Philadelphia, 1998
29. Michailidis GD, Papageorgiou P, Economides DL. Assessment of fetal anatomy in the first trimester using two­and three-dimensional ultrasound. Br J Radiol 2002;75:215–219
30. Monteagudo A, Reuss ML, Timor-Tritsch IE. Imaging the fetal brain in the second and third trimester using transvaginal sonography. Obstet Gynecol 1991;77:27–32
31. Monteagudo A, Timor-Tritsch IE. First trimester anatomy scan: pushing the limits. What can we see now? Current Opin Obstet Gynecol 2003;15:131–141
32. Moore TR. Superiority of the four-quadrant sum over the single-deepest-pocket technique in ultrasonographic identification of abnormal amniotic fluid volumes. Am J Obstet Gynecol 1990;163:762–767
33. Nelson TR, Downey DB, Pretorius DH, Feuster A. Three-dimensional ultrasound. Lippincott Williams and Wilkins, Philadelphia, 1999
34. Nicolaides KH. Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities. Am J Obstet Gynecol 2004;191:45–67
35. Nyberg DA, Hill LM, Bohm-Velez M, Mendelson EB. Transvaginal ultrasound. Mosby-Yearbook, St Louis, MO, 1992
36. Odwin CS, Fleischer AC, Kepple DM. Probe covers and disinfectants for transvaginal transducers. J Diagn Med Sonogr 1990;6:130–135
37. Rizzo G, Capponi A, Angelini E, Vlachopoulou A, Grassi C, Romanini C. The value of transvaginal ultrasonographic examination of the uterine cervix in predicting preterm delivery in patients with preterm premature rupture of membranes. Ultrasound Obstet Gynecol 1998;11:23–29
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38. Rottem S, Thaler I, Goldstein SR, Timor­Tritsch IE, Brandes JM. Transvaginal sonographic technique: targeted organ scanning without resorting to ‘planes.’ J Clin Ultrasound 1999;18:243–247
39. Rutherford SE, Phelan JP, Smith CV, Jacobs N. The four-quadrant assessment of amniotic fluid volume: an adjunct to antepartum fetal heart rate testing. Obstet Gynecol 1987;70:353–356
40. Sabbagha RE. Diagnostic ultrasound applied to obstetrics and gynecology, 3rd edn. Lippincott, Philadelphia, 1994
41. Scanlan KA, Pozniak MA, Fagerholm M, Shapiro S. Value of transperineal sonography in the assessment of vaginal atresia. Am J Roentgenol 1990;154:545–548
42. Souka AP, Nicolaides KH. Diagnosis of fetal abnormalities at the 10–14-week scan. Ultrasound Obstet Gynecol 1997;10: 429–442
43. Souka AP, Pilalis A, Kavalakis I et al.
Ultrasound in obstetrics and gynaecology
Assessment of fetal anatomy at the 11–14­week ultrasound examination. Ultrasound Obstet Gynecol 2004;24:730–734
44. Spencer K, Nicolaides KH. Screening for trisomy 21 in twins using first trimester ultrasound and maternal serum biochemistry in a one-stop clinic: a review of three years experience. Br J Obstet Gynaecol 2003;110:276–280
45. Tekay A, Jouppila P. Blood flow in benign ovarian tumors and normal ovaries during the follicular phase. Obstet Gynecol 1995;86:55–59
46. Tekay A, Jouppila P. Controversies in assessment of ovarian tumors with transvaginal color Doppler ultrasound. Acta Obstet Gynecol Scand 1996;75:316–329
47. Tekay A, Jouppila P. Intraobserver variation in transvaginal Doppler blood flow measurements in benign ovarian tumors. Ultrasound Obstet Gynecol 1997;9: 120–124
48. Tessler F, Schiller VL, Perrella RR et al. TAS versus endovaginal pelvic sonography: prospective study. Radiology 1980;170: 553–556
49. Timmerman D, Valentin L, Bourne TH et al. Terms, definitions and measurements to describe the sonographic features of adnexal tumors: a consensus opinion from the International Ovarian Tumor Analysis (IOTA) Group. Ultrasound Obstet Gynecol 2000;16:500–505
50. Timor-Tritsch IE, Bar-Yam Y, Elgali S, Rottem S. The technique of TVS
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sonography with the use of 6.5 MHz probe. Am J Obstet Gynecol 1988;158:1019–1024
51. Timor-Tritsch IE, Bashiri A, Monteagudo A, Arslan AA. Qualified and trained sonographers in the US can perform early fetal anatomy scans between 11 and 14 weeks. Am J Obstet Gynecol 2004;191:1247–1252
52. Timor-Tritsch IE, Haratz-Rubinstein N, Monteagudo A, Lerner JP, Murphy K. Transvaginal color Doppler sonography of the ureteral jets: a potential method to detect ureteral obstruction. Obstet Gynecol 1997;89:113–117
53. Timor-Tritsch IE, Haratz-Rubinstein N, Murphy K, Monteagudo A. Transvaginal ultrasound in the detection of ureteral jets. Contemporary Reviews in Obstetrics and Gynecology 1997;143–148
54. Timor-Tritsch IE, Lerner JP, Monteagudo A, Murphy KE, Heller DS. Sonographic markers of inflammatory tubal disease. Ultrasound Obstet Gynecol 1998;12:56–66
55. Timor-Tritsch IE, Monteagudo A, Rebarber A et al. Transrectal scanning: an alternative when transvaginal scanning is not feasible. Ultrasound Obstet Gynecol 2003;21: 473–479
56. Timor-Tritsch IE, Monteagudo A. Transvaginal fetal neurosonography: standardization of the planes and sections used by anatomic landmarks. Ultrasound Obstet Gynecol 1996;8:42–47
57. Timor-Tritsch IE, Rottem S (eds) Transvaginal sonography, 2nd edn. Elsevier, New York, 1991
58. Timor-Tritsch IE. Standardization of ultrasonographic images: let's all talk the same language! Ultrasound Obstet Gynecol 1992;2:311–312
59. Ueland FR, DePriest PD, Pavlik EJ, Kryscio RJ, van Nagell JR Jr. Preoperative differentiation of malignant from benign ovarian tumors: the efficacy of morphology indexing and Doppler flow sonography. Gynecol Oncol 2003;91:46–50
60. Whitlow BJ, Chatzipapas IK, Lazanakis ML, Kadir RA, Economides DL. The value of sonography in early pregnancy for the detection of fetal abnormalities in an unselected population. Br J Obstet Gynaecol 1999;106:929–936
61. Zimmer EZ, Timor-Tritsch IE, Rottem S. The technique of transvaginal sonography. In: Timor-Tritsch IE, Rottem S (eds) Transvaginal sonography, 2nd edn. Elsevier, New York, 1991
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Investigation of early pregnancy

Harm-Gerd K Blaas José M Carrera
ABSTRACT
The preferred approach for the first-trimester examination is transvaginal sonography (TVS) although transabdominal sonography (TAS) could be and sometimes should be used to get a better overview. The presentation of images made by TVS and TAS should be standardized.
In early pregnancy, use established measurement methods and measure several parameters: the crown–rump length (CRL), the head width, the heart rate, the diameter of the amniotic cavity and the diameter of the yolk sac; if possible, describe the anatomy. Looking at the heart activity alone is an incomplete examination.
A detailed description of the embryonic development starting at week 4 and ending at week 10 is presented.
KEYWORDS
Early pregnancy loss, ectopic pregnancy, first trimester ultrasound, miscarriage, sonoembryology.

INTRODUCTION

Approximately 12–15% of all pregnancies end in recognizable miscarriages.1 The most common indication for emergency referral in early pregnancy is vaginal bleeding. However, there are many other reasons for a pregnant woman to visit her doctor, such as abdominal pain, poor obstetric history, recurrent miscarriages, previous pregnancy with anomalous embryonic/fetal development, check-up fol­lowing assisted fertilization, possible teratogenic exposure, uncertain gestational age or general anxiety. Today an ultrasound assessment of the pregnancy is a natu­ral part of a first-trimester clinical examination.
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An ultrasound examination in the first trimester is expected to provide answers to important questions. Is the embryo/young fetus alive? Is the pregnancy prop­erly located in the cavity of the uterus? Is it a single or multiple pregnancy, and in cases of multiple pregnancy, what is the chorionicity and amnionicity? What is the age of the conceptus? The examiner must recognize the signs of early preg­nancy failure such as embryonic demise, spontaneous abortion, ectopic pregnancy, hydatidiform mole, and be able to identify normal anatomy and/or anomalies in very early viable pregnancies.
2
The characteristics of the early conceptus are its small size, its constantly changing anatomical appearance, and its uniform development and constant growth. Therefore, the prerequisite for any early scan, in addition to adequate ultrasound equipment, is a thorough knowledge of the normal sonographic appearance of the developing embryo and its associated structures.2 The transvaginal approach is preferred.
In this chapter, fetal age is always given in completed weeks and completed days based on the last menstrual period, i.e. the standard in obstetrics.
Ultrasound in obstetrics and gynaecology

DESCRIPTION OF THE SONOANATOMIC DEVELOPMENT

During the last two decades, systematic ultrasound studies have provided impor­tant and extensive knowledge about the development of the living embryo up to 10 weeks and the young fetus from 10 weeks on with detailed anatomic descrip­tions of embryonic organs and extraembryonic structures.
39
58
4.5 weeks
After approximately 4.5 weeks (LMP-based), a tiny gestational sac (diameter 2 mm) becomes visible within the decidua surrounded by the echogenic tropho­blastic ring.
5 weeks 0–6 days, CRL ª0–3 mm
At 5 weeks the thin-walled yolk sac usually appears (Fig. 4.1). After 5.5 weeks the yolk sac is always visible, which indicates that the pregnancy is properly located in the uterine cavity, even if the embryo is not yet identified. The embry­onic pole appears adjacent to the yolk sac. Since the connecting stalk is short, the embryonic pole is located near the wall. The heart rate is about 80–100 beats per minute (bpm) at the end of this week.
6 weeks 0–6 days, CRL ª4–8 mm
The embryonic pole, yolk sac and the heart activity are always present. The heart rate increases to 130 bpm (Fig. 4.2).
7 weeks 0–6 days, CRL ª9–14 mm
In sagittal section, the embryonic body appears as a triangle. The sides consist of the back and the roof of the rhombencephalon, and the frontal part includes the head, the basis of the umbilical cord, and the embryonic tail (Fig. 4.3). The embry- onic body is slender in the coronal plane. The limbs appear as short hypoechogenic
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Chor cavity
Yolk sac
Embryo
Heart
Fig. 4.1 5 weeks 1 day old pregnancy: retroverted uterus, trophoblastic ring in fundus; (arrow) small secondary yolk sac.
Investigation of early pregnancy
Fig. 4.2 6 weeks 1 day old pregnancy: CRL 5.2 mm. The embryo and the yolk sac lie close to the wall (future placenta). The beating heart can easily be identified by real-time ultrasound.
outgrowths. The hypoechogenic brain cavities can be seen. The shallow rhomben­cephalic cavity is also visible from 7 weeks on. It has a well-defined rhombic shape in the cranial pole of the embryo. The heart can easily be recognized by real-time ultrasound as a relatively large beating structure below the embryonic head. It is large and echogenic, the frequency has increased from 130 to 160 bpm. The thin amniotic membrane surrounding the embryo becomes visible. The mean diameter of the amniotic cavity is approximately identical with the CRL.
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Rhombencephalon
Mesencephalon
Diencephalon
A
B
Ultrasound in obstetrics and gynaecology
Fig. 4.3 7 weeks, CRL 13 mm. (A) Sagittal section through body; dotted line = section of B. (B) Horizontal section through the head showing measurement of head width and OFD (occipitofrontal diameter).
8 weeks 0–6 days, CRL ª15–22 mm
The brain cavities are easily seen as large ‘holes’ in the embryonic head (Fig. 4.4). Choroid plexuses become visible as echogenic areas in the enlarged lateral ventri­cles and in the roof of the fourth ventricle. The third ventricle is still rather wide, as is the mesencephalic cavity. The mesencephalon is on top of the head. The spine is seen as two echogenic parallel lines. It is possible to recognize the fluid­filled stomach as a small hypoechogenic area on the left side of the upper abdo­men below the heart. The physiological herniation of the gut can be identified as an echogenic area in the umbilical cord at the abdominal insertion. Within a few days, this echogenic structure becomes more distinct. At the end of the week, the fingers may be distinguishable.
9 weeks 0–6 days, CRL ª23–31 mm (Fig. 4.5)
At week 9 it is possible to obtain acceptable images of the embryonic pro­file. The lateral ventricles are always visible. They are best seen in the parasag­ittal plane, where the C-shape becomes apparent. The bright choroid plexuses of the lateral ventricles are regularly detectable at 9 weeks. The width of the
60
diencephalic cavity narrows gradually while the mesencephalon remains wide.
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Chorionic cavity
Amn cavity
Rhomb
Mes
Umb
Lower
limb
3. ventr
Amn cavity
Mes
Lat
ventr
Lower
limb
3. ventr
Lower
limb
Investigation of early pregnancy
Fig. 4.4 8/1 weeks, CRL 15 mm, sagittal section through embryo lying in amniotic cavity; the dotted line indicates section of image on the right side, horizontal section through the head. Mes, mesencephalic cavity; Rhomb, rhombencephalic cavity.
The choroid plexuses of the fourth ventricle are echogenic landmarks which divide the fourth ventricle into a rostral and a caudal compartment. The cer­ebellar hemispheres are easily detectable. The spine is still characterized by two echogenic parallel lines. During week 9 the heart rate reaches a maximum of mean 175 bpm. The midgut herniation is now a large hyperechogenic mass in the umbilical cord (Fig. 4.6).
10 weeks 0–6 days, CRL ª32–42 mm, and 11 weeks 0–6 days, CRL ª43–54 mm
The fetus has developed a human appearance. The head is relatively large with a marked chin, a prominent forehead and a flat occiput. Ossification starts at about 11 weeks with the occipital bone,10 then the ossification of the spine becomes apparent. The lateral ventricles fill the anterior part of the head and conceal the diencephalic cavity. The cerebellar hemispheres seem to meet in the midline dur­ing weeks 11 and 12. The heart rate slows down to 165 bpm at the end of week
11. Anatomical details of the heart become obvious. The midgut herniation has its maximal extension at the beginning of week 10; it returns into the abdominal cavity during weeks 10–11. Fetuses that are older than 12 weeks do not dem­onstrate any sign of the midgut herniation. The stomach is always visible at 11 weeks. During weeks 9–11 the shape of the yolk sac alters and its wall becomes thinner. The yolk sac enlarges in some cases, while in other cases it shrinks.
9
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Echogenic midgut herniation in umbilical cord
A
B
Echogenic midgut herniation in umbilical cord
Cord cyst (normal phenomenon in early first trimester)
Body
Chorionic cavity
Amniotic cavity
Choroid plexus of 4th ventricle
Mesencephalic cavity
3rd ventricle
Spine
Ultrasound in obstetrics and gynaecology
Fig. 4.5 Approximately 9-week-old embryo, CRL 22 mm, sagittal section through the embryo in the amniotic cavity.
62
Fig. 4.6 Sagittal (A) and horizontal (B) section through an embryo (CRL 28 mm) at the end of week 9. The midgut herniation of the bowel is identified as an echogenic area in the umbilical cord. In (B) horizontal section through the embryonic abdomen; the arrows point at the abdominal insertion of the umbilical cord, containing echogenic bowel.