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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5786_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Contributors
- •Preface
- •1. Physics and instrumentation
- •Introduction
- •Sound
- •Short History of the Development of Ultrasound in Medicine
- •Near Field and Far Field
- •Focusing
- •Sound, Waves and Propagation
- •One Transducer for Each Purpose
- •The Ultrasound Beam
- •Resolution
- •Measurement
- •Time Gain Compensation
- •Artifacts
- •Edge Shadows
- •Attenuation Shadows
- •Enhancement
- •Reverberations
- •References
- •Further reading
- •2. Biological effects and safety aspects
- •Introduction
- •Acoustic Output of Diagnostic Ultrasound Scanners
- •Tissue Warming by Diagnostic Ultrasound
- •Non-Thermal Mechanisms and their Safety Implications
- •Gas Body Effects of Diagnostic Ultrasound
- •Other Mechanical Bioeffects Mechanisms
- •Evidence from Epidemiology
- •The Management of Safety
- •The Users' Responsibility
- •Thermal indices
- •Mechanical index
- •The Manufacturers' Obligations
- •Safety Practice
- •Diagnostic Ultrasound During the First Trimester
- •Scanning During the Second and Third Trimesters
- •Obstetric Scanning on Patients with Fever
- •Conclusion
- •References
- •3. Scanning techniques in obstetrics and gynaecology
- •Introduction
- •General Aspects
- •Empty or Full Bladder
- •Patient Information
- •The Examination Table
- •Bimanual Pelvic Examination Preceding the Scan
- •Equipment
- •Orientation
- •Scanning Routine
- •Obstetric Scanning
- •Biophysical profile
- •Gynaecological Scanning
- •The uterus
- •The cervix
- •The myometrium
- •The endometrium
- •Adnexal Masses
- •Peritoneal Fluid
- •Urinary Bladder
- •Other Findings
- •Colour Doppler Studies
- •Screening for Ovarian Masses
- •Transperineal and Transrectal Scanning
- •Ultrasound-Guided Puncture Procedures
- •Conclusion
- •References
- •4. Investigation of early pregnancy
- •Introduction
- •Description of the Sonoanatomic Development
- •Measurements of the Embryo/Early Fetus
- •Extraembryonic Structures: The Three Sacs
- •Multiple Pregnancy: Determination of Chorionicity and Amnionicity
- •Evaluation of Early Pregnancy Failure
- •Early Pregnancy Loss
- •Gestational sac (chorionic cavity) and amniotic cavity
- •Yolk sac
- •Haematoma
- •Heart rate
- •Trophoblastic Disease
- •Complete hydatidiform mole
- •Partial hydatidiform mole
- •Invasive hydatidiform mole
- •Choriocarcinoma
- •Ectopic Pregnancy
- •Early Anomalies
- •Standardization of Transvaginal and Transabdominal Imaging in Gynaecology
- •Imaging in Medicine
- •References
- •5. Normal fetal anatomy at 18–22 weeks
- •Introduction
- •Scan Guidelines
- •Normal Fetal Anatomy
- •Brain/Calvarium
- •Transthalamic view
- •Transventricular view
- •Heart
- •Transcerebellar view
- •Face and Neck
- •Spine
- •Lungs and Thorax
- •Abdomen
- •Anterior Abdominal Wall
- •Urinary Tract
- •Genitalia
- •Skeleton and Extremities
- •Conclusion
- •References
- •6. Amniotic fluid and placental localization
- •Amniotic Fluid
- •Amniotic Fluid Physiology
- •Fetal urinary production
- •Lung fluid
- •Flow across the chorionic plate
- •Amniotic Fluid Volume
- •Methods of assessment
- •Normal amniotic fluid volume values
- •Abnormal amniotic fluid volumes
- •Oligohydramnios
- •Polyhydramnios
- •Conclusions
- •Placenta Localization
- •Embryology
- •Functional anatomy
- •Development of the placenta as evaluated by ultrasound technology
- •Indications for the Location of the Placenta
- •Various locations of the placenta
- •Placenta praevia
- •Suggested management protocol for suspected placenta praevia
- •Placental Morphology
- •Conclusion
- •References
- •7. Assessment of the placenta and umbilical cord
- •Introduction
- •Major Structural Abnormalities of the Placenta
- •Congenital Abnormalities
- •Abnormalities of placentation
- •Placenta extrachorialis
- •Placenta accreta
- •Placental tumours
- •Mesenchymal tumours
- •Gestational trophoblastic tumours (GTD)
- •Secondary Abnormalities
- •Vascular abnormalities
- •Thrombosis and infarcts
- •Haematomas
- •Major Structural Abnormalities of the Umbilical Cord
- •Congenital Abnormalities
- •Abnormalities of the cord insertion
- •Single umbilical artery (SUA) syndrome
- •Cord tumours
- •Secondary Abnormalities
- •Vascular abnormalities
- •Haematomas and thrombosis
- •Vascular abnormalities
- •Abnormal cord position
- •References
- •8. Examining the cervix by transvaginal ultrasound
- •Introduction
- •Transvaginal Ultrasound of the Cervix Predicts Preterm Delivery
- •Measurement Technique
- •Transvaginal Ultrasound of the Cervix in the Clinical Judgement of Preterm Labour
- •Treatment of Cervical Incompetence
- •Prophylactic Cerclage or Transvaginal Follow-Up of the Cervix
- •Prophylactic Treatment with Progesterone in Pregnant Women with Short Cervix
- •Conclusion
- •References
- •9. Fetal biometry, estimation of gestational age, assessment of fetal growth
- •Principles of Fetal Biometry
- •Aims of Fetal Biometry
- •The Reference Values
- •Patient Selection and Study Design
- •Longitudinal and Cross-Sectional Studies
- •Sample Size
- •Displaying Data and Curve Fitting
- •Linear regression analysis
- •Curvilinear regression analysis
- •The coefficients of correlation
- •The F test
- •Prediction of Date and Size
- •The Confidence Limits
- •Dating
- •Menstrual, Conceptual and Gestational Age
- •Errors of Measurements
- •The Accuracy of Dating
- •Biometric Parameters
- •Gestational Sac
- •Crown–Rump Length
- •Head Measures
- •Abdominal Size
- •Limbs
- •Other Measurements and Dating
- •Data Report
- •Fetal Weight Estimation
- •Biometric Ratios
- •Other Parameters
- •Evaluation of Fetal Growth
- •Definition
- •Unsolved Problems
- •Screening and Diagnostic Strategies
- •Fetal Growth Restriction
- •Macrosomia
- •Fetal Biometry, Anomalies and Syndromes
- •Conclusion
- •References
- •10. Prenatal diagnosis of fetal anomalies
- •An Introduction to Congenital Anomalies
- •Central Nervous System Anomalies
- •Neural Tube Defects
- •Ventriculomegaly
- •Holoprosencephaly
- •Agenesis of the Corpus Callosum
- •Dandy–Walker Complex
- •Microcephaly
- •Destructive Cerebral Lesions
- •Choroid Plexus cysts
- •Craniofacial Anomalies
- •Facial Clefts
- •Ocular and Orbital Defects
- •Cardiac Anomalies
- •Atrial and Ventricular Septal Defects
- •Atrioventricular septal defects
- •Heterotaxy
- •Univentricular Heart
- •Aortic Stenosis
- •Coarctation, Tubular Hypoplasia and Interruption of the Aortic Arch
- •Hypoplastic Left Heart Syndrome
- •Pulmonary Stenosis and Pulmonary Atresia
- •Conotruncal Malformations
- •Ebstein's Anomaly and Tricuspid Valve Dysplasia
- •Echogenic Foci
- •Cardiac Dysrhythmias
- •Thoracic Anomalies
- •Hyperechogenic and Cystic Lungs
- •Pleural effusions
- •Diaphragmatic Hernia
- •Anomalies of the Abdominal Wall and Gastrointestinal Tract
- •Omphalocele
- •Gastroschisis
- •Body Stalk Anomaly
- •Bladder Exstrophy and Cloacal Exstrophy
- •Oesophageal Atresia
- •Duodenal Atresia
- •Intestinal Obstruction
- •Echogenic Bowel
- •Meconium Peritonitis
- •Abdominal Cysts
- •Anomalies of the Kidneys and Urinary Tract
- •Renal Agenesis
- •Cystic Kidneys
- •Urinary Tract Enlargement
- •Skeletal Anomalies
- •Fetal Tumours
- •Hydrops Fetalis
- •Chromosomal Defects
- •Ultrasound Findings with Chromosomal Aberrations
- •Individual Risk Assessment of Chromosomal Aberrations by the use of Midtrimester Ultrasound
- •Absent or hypoplastic nasal bone (<2.5 mm)
- •Nuchal oedema or fold more than 6mm
- •Hyperechogenic bowel
- •Short femur
- •Echogenic foci in the heart
- •Choroid plexus cysts
- •Mild hydronephrosis
- •Accuracy of Ultrasound in the Detection of Fetal Anomalies
- •Conclusion
- •Note
- •References
- •11. Evaluation of fetal and uteroplacental blood flow
- •Introduction
- •Uterine Artery Doppler
- •Umbilical Artery Doppler
- •Middle Cerebral Artery Doppler
- •MCA in Fetal Growth Restriction
- •MCA in Fetal Anaemia
- •Ductus Venosus
- •Umbilical Vein
- •Doppler in Twin Pregnancies
- •References
- •12. Invasive procedures in obstetrics
- •Introduction
- •Counselling
- •Training
- •The Procedures
- •Asepsis
- •Chorionic Villous Sampling
- •Chorionic villus sampling in multiple gestations
- •Safety
- •Amniocentesis
- •Safety
- •Amniocentesis in multiple gestations
- •Fetal Blood Sampling
- •Technique
- •Complications
- •Intrauterine Fetal Blood Transfusion
- •Complications
- •Fetal Shunts
- •Techniques
- •Complications
- •Delivery and shunt removal
- •Outcome
- •Diagnostic and Operative Fetoscopy
- •Pregnancy Reduction in Multifetal Pregnancies
- •Technique
- •Selective Fetocide for Fetal Abnormality
- •Conclusion
- •References
- •13. Multiple pregnancies
- •Introduction
- •First-Trimester Ultrasound
- •Pregnancy Dating
- •Number of Fetuses
- •Chorionicity and Amnionicity
- •Nuchal Translucency
- •Invasive Diagnostic Procedures
- •Growth Discrepancy and Fetal Monitoring
- •Malformations and Fetal Demise
- •Twin–Twin Transfusion Syndrome
- •Twin Reversed Arterial Perfusion
- •Monoamniotic Twins
- •Higher-Order Multiple Pregnancies
- •References
- •14. Three-dimensional and four-dimensional ultrasound application in prenatal diagnosis
- •Introduction
- •Volume Acquisition
- •Static 3D
- •Real-Time 3D or 4D Ultrasound
- •Spatial and Temporal Image Correlation
- •Volume Data Display
- •Single Plane of Choice, Multiplanar Orthogonal Planes or Multiple Tomographic Parallel Slices
- •Surface Mode Rendering
- •Maximum Mode Rendering
- •Minimum Mode Rendering
- •Inversion Mode Rendering
- •Glass Body Mode Rendering
- •Volume Calculation
- •Conclusion
- •References
- •15. Fetal movement patterns and behavioural states
- •Introduction
- •Methodology
- •The Emergence of Fetal Movement Patterns
- •Body Movements in Normal Pregnancy
- •Fetal Breathing in Normal Pregnancy
- •Normal Development of Fetal Behavioural States
- •Altered Brain or Muscular Development
- •Intrauterine Growth Retardation (IUGR)
- •Maternal Diabetes
- •Preterm Contractions and/or Rupture of Membranes
- •Drugs, Medication, Stress and Fetal Stimulation
- •Conclusion
- •References
- •16. Normal gynaecological anatomy (uterus, tubes, ovaries)
- •Introduction
- •Normal Ultrasound Morphology of the Cervix Uteri
- •Normal Ultrasound Morphology of the Uterus in Women of Fertile Age
- •Normal Ultrasound Morphology of the Ovaries in Women of Fertile Age
- •Normal Ultrasound Morphology of the Uterus and Ovaries in Postmenopausal Women
- •Normal Ultrasound Morphology of the Uterus and Ovaries in Menopausal Transition
- •Normal Uterine and Ovarian Vascularization as Assessed by Doppler Ultrasound Technique
- •The Tubes
- •The Pouch of Douglas
- •Hydrosonography
- •Hystero-Contrast Salpingosonography (HyCoSy)
- •Acknowledgements
- •References
- •17. Gynaecological pathology: the uterus
- •Introduction
- •Congenital Uterine Anomalies
- •Uterine Fibroids
- •Uterine Sarcoma
- •Adenomyosis
- •Endometrial Polyps
- •Endometrial Hyperplasia and Malignancy
- •Conclusion
- •References
- •18. Gynaecological pathology: tubes and ovaries
- •Ovaries
- •Benign and Malignant Ovarian Cysts: General Considerations
- •Tumour Size
- •Tumour Structure
- •Cyst Wall and Septal Wall Thickness
- •Echo-Dense Foci and Acoustic Shadowing
- •Echogenicity
- •Morphology Scoring Systems
- •Benign and Malignant Neoplasms of the Ovary
- •Dysfunctional ovarian cysts
- •Follicle cysts
- •Corpus luteum cysts
- •Thecalutein cysts
- •Endometriosis
- •Epithelial ovarian tumours
- •Serous ovarian tumours
- •Mucinous ovarian tumours
- •Fibromas and fibrothecomas
- •Germ cell tumours
- •Adnexal Torsion
- •Tubes
- •Non-Infectious Diseases of the Fallopian Tubes
- •Tubal pregnancy
- •Fallopian tube carcinoma
- •Hydrosalpinx
- •Infectious Diseases of the Fallopian Tubes
- •Note
- •References
- •19. Doppler ultrasonography in gynaecology
- •Introduction
- •Adnexal Masses
- •Other Pelvic Pathology
- •In Vitro Fertilization
- •References
- •20. Medico-legal implications of ultrasound imaging in obstetrics and gynaecology
- •Introduction
- •The Legal Process
- •The Trial Process
- •Reducing the Risk of Litigation
- •Never undertake a type of scan with which you are not entirely familiar (unless in a learning environment)
- •Record sample images (and be able to retrieve them)
- •Always act professionally and responsibly
- •Be aware of the common traps (and avoid them!)
- •If the scan is suboptimal, say so and explain why
- •Ensure the equipment is appropriate
- •Defending a Claim
- •Recording Images
- •Documentation
- •Conclusion
- •21. Ethics and patient information
- •Introduction
- •Ethics, Medical Ethics and Ethical Principles
- •The Principle of Beneficence
- •The Principle of Respect for Autonomy
- •The Interaction of Beneficence and Respect for Autonomy in Clinical Judgement and Practice
- •The Ethical Concept of the Fetus as a Patient
- •The viable fetal patient
- •The previable fetal patient
- •Clinical Topics
- •Competence and Referral in Ultrasound Examination
- •Routine Ultrasound Screening and Risk Assessment of Pregnant Women
- •Disclosure of Results of Ultrasound Examinations
- •Confidentiality of Findings
- •Conclusion
- •References
- •Test yourself – questions and answers
- •Chapter 2 Biological Effects and Safety Aspects
- •Chapter 4 Investigation of Early Pregnancy
- •Chapter 5 Normal Fetal Anatomy at 18–22 Weeks
- •Chapter 6 Amniotic Fluid and Placental Localization
- •Chapter 10 Prenatal Diagnosis of Fetal Anomalies
- •Chapter 12 Invasive Procedures in Obstetrics
- •Chapter 13 Multiple Pregnancies
- •Chapter 17 Gynaecological Pathology: The Uterus
- •Chapter 19 Doppler Ultrasonography in Gynaecology
- •Chapter 21 Ethics and Patient Information
- •Answers
- •Index

✩✩✩✩✩✩✩✩✩✩✩ ✩
to about 350 mL at 42 weeks of gestation. Oligohydramnios may also develop
in association with drug therapies such as indometacin treatment in premature labour. Decreased renal perfusion may be the underlying mechanism for
this. Another cause of oligohydramnios is premature rupture of the membranes
(PROM), which occurs in approximately 10% of all pregnancies and is associated with increased perinatal mortality and morbidity due to premature labour,
chronic fetal distress or infection. When severe oligohydramnios develops before
20–25 weeks of gestation, there is a high association with fetal pulmonary hypoplasia, fetal facial compression and abnormal position/contractures of hands/feet
(oligohydramnion sequence).
Polyhydramnios
Polyhydramnios is defined as a deepest fluid pocket of more than 8 cm or an
amniotic fluid index of at least 25 cm or more. Its incidence has been reported
to range from 0.4% to 3.3%. Chronic polyhydramnios which develops gradually
over weeks or months is more common than acute polyhydramnios.
The aetiology of polyhydramnios is diverse and includes fetal congenital anomalies, notably neural tube defects and neuromuscular defects preventing adequate
swallowing, on the one hand, and gastrointestinal obstruction resulting in fluid
congestion on the other. Nearly one in five pregnancies with chronic polyhydramnios has been associated with fetal anomalies. Other abnormal maternal and
fetal conditions associated with polyhydramnios are maternal diabetes mellitus,
macrosomia, multiple pregnancy and non-immune fetal hydrops. Also, lesions
of the umbilical cord and placenta have been associated with polyhydramnios.
However, in approximately two-thirds of pregnancies with polyhydramnios, no
specific cause can be established. Idiopathic polyhydramnios12 does not seem to
be less associated with adverse perinatal outcomes than polyhydramnios in which
one of the above fetal or maternal conditions has been identified. Polyhydramnios
in itself may create obstetric problems such as premature labour, postpartum
haemorrhage and PROM resulting in prolapsed cord.
Amniotic fluid and placental localization
CONCLUSIONS
Various pathways determine production and absorption of amniotic fluid, amongst
which are fetal swallowing, fetal urinary production, fetal lung fluid excretion,
fluid transfer through the chorionic plate and to a minor extent fluid excretion by
the fetal salivary glands. Normal amniotic fluid volumes display a wide distribution with a marked increase up to about 34 weeks and a gradual reduction thereafter. Determination of amniotic fluid volume includes single deepest pocket and
amniotic fluid index measurement. Abnormal amniotic fluid volumes include
both oligohydramnios and polyhydramnios. Whereas oligohydramnios is mostly
associated with fetal pathology, polyhydramnios may be due to abnormal fetal or
maternal conditions or may be idiopathic. The predictive value of amniotic fluid
index and single deepest amniotic fluid pocket for oligo- and polyhydramnios
appears to be limited.
113

✩ ✩✩✩✩✩✩✩✩✩✩✩
Chorion
frondosum
Decidua
basalis
Decidua
parietalis
Decidua
capsularis
Chorion laeve
Measurement of the vertical diameter in each of the four quadrants of the
uterus is undertaken. The numbers are added up to calculate the amniotic fluid
index.
PLACENTA LOCALIZATION
The introduction of ultrasound technology represented a unique step forward in
our ability to make a diagnosis regarding the human placenta. Rapidly, it became
clear that the new technology had far more advantages than x-ray, thermography
and scintigraphy in the ability to locate the placenta, and it left the old techniques
obsolete. Even the particularly difficult problem of defining the exact delineation
of the border in cases where placenta praevia was suspected is now of historical
interest only as a consequence of high-resolution ultrasound and the transvaginal
scanning approach.
EMBRYOLOGY
Ultrasound in obstetrics and gynaecology
The placenta is regarded as an organ of fetal origin as it develops solely from
the outer cell layer of the blastocyst, the trophoblast. The contact with the uterine endometrium and the trophoblast induces a proliferation of the trophoblast.
Some of the trophoblast cells lose their cell membrane and form a syncytium, the
so-called syncytioblast. This process stimulates a decidual reaction in the endometrium that causes the stroma to become thicker and highly vascularized, then
called decidua. A thin capsule of the decidua called decidua capsularis covers the
part of the embryo which is protruding into the endometrial cavity. The decidua
at the embryonic pole develops into the decidua basalis, which takes part in the
formation of the future placenta. During early development, the vessels supporting the decidua capsularis regress and the smooth chorion or chorion laeve develops.6 The vessels supporting the decidua basalis are retained and the leafy chorion
or chorion frondosum is developed and the growth process of the placenta, which
takes most of the remaining time of the pregnancy, then commences (Fig. 6.2).
114
Fig. 6.2 Status of the chorion and the decidua at approximately 8 weeks' gestational age.

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Functional anatomy
The human placenta is the interface between the circulations of the mother and
fetus for the exchange of nutrients, respiratory gases and waste products.3 The
physiological mechanism of the transfer of specific substances is complicated and
remains a field for advanced research. This is in contrast to other organ systems
where such a mechanism is mostly understood.
The human placenta has approximately 120 cotyledons that together comprise the functional unit of the organ. Each of these cotyledons has a primary
villus stem which arises from the chorionic plate and is supplied by the primary
branches of the fetal vessels. Further down the vascular tree, these branches form
the secondary and tertiary stem where the vascular exchange takes place. From
the maternal side, the pulsative blood flow from the spiral arteries enters the
intercotyledonary space and flushes the maternal side of the vascular space all
the way up to the chorionic plate. Between the cotyledons, the blood filters into
venous channels and returns to the decidual plate. There is complete separation
between the fetal and the maternal blood and all exchange of nutrients and blood
gases takes place through the vasculosyncytial membranes separating the two
circulatory systems.
Development of the placenta as evaluated by ultrasound technology
During weeks 8–12 the development of the placenta may be followed and the
chorion frondosum (placenta) may be easily differentiated from the chorion laeve
(chorion) (Fig. 6.3). From week 12 onwards it becomes possible to differentiate
between the placenta, the basal plate facing the maternal side of the placenta and
the chorionic plate facing the fetus. The placenta grows as pregnancy progresses,
allowing easy identification.
Amniotic fluid and placental localization
INDICATIONS FOR THE LOCATION OF THE PLACENTA
First-trimester invasive procedures such as abdominal or transvaginal
•
chorion villus biopsy
Transabdominal amniocentesis in the second trimester and other invasive
•
procedures performed any time later in the pregnancy
Bleeding in the second and third trimesters
•
Evaluation of the placenta and its location and relation to the uterine wall
•
in cases of suspected placental abruption
Routine fetal examination performed at 18–20 weeks
•
Prior to external version of the fetus in late pregnancy.
•
The most common indication for location of the placenta is during systematic
evaluation of the uterus and the intrauterine contents during the second-trimester fetal examination or ‘routine fetal examination’ as it is frequently called. The
fetal examination is best initiated by the inverted U-movement of the transducer
starting at the symphysis, slowly moving the transducer in a transverse plane on
one side of the uterus to the top of the uterus and then down to the symphysis
115

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Fig. 6.3 Pregnancy at 10 weeks' gestational age. The placenta and the chorion are clearly imaged,
as is the amniotic sac surrounding the fetus. The amnion has not yet fused with the chorion.
on the contralateral side. During this procedure the placenta may be located and
other important features such as the viability of the fetus, the position and the
Ultrasound in obstetrics and gynaecology
number of fetuses may be established.
In early pregnancy, i.e. before the 18–20-week routine fetal examination, there
is no reason to register the location of the placenta except for those indicated
above.
116
Various locations of the placenta
In the second trimester, the chorionic plate or the fetal surface of the placenta
is usually seen as a white line. The placenta is usually relatively echogenic, with
equally distributed, fine-grained echoes through the full extent of the organ. The
basal plate is not always easy to distinguish but the uterine tissue, which is about
1.5 cm thick, appears slightly darker in its fine-grained echo setting compared to
the placenta, making the delineation between the placenta and the uterine tissue possible (Fig. 6.4). Normally, the placenta is located in the fundal area on the
left or right lateral side, the posterior or the anterior side (Fig. 6.5) or a combination thereof. The most important clinically useful distinction of the location is
Fig. 6.4 Placenta located on the anterior wall. The uterine wall, the basal plate of the
placenta facing the uterus and the chorionic plate facing the fetus are clearly seen.

✩✩✩✩✩✩✩✩✩✩✩ ✩
Fig. 6.5 Placenta located on the anterior wall including a velamentous insertion of the cord.
Amniotic fluid and placental localization
the relation between the lower portions of the placenta and the internal os of the
uterus (Fig. 6.6). Attempts should be made to demonstrate the lower portion of
the placenta and the internal os on the same image. Care must be taken to distinguish between Braxton Hicks contractions and the placenta. The contraction
appears darker and less echogenic (Fig. 6.7).
The final location of the placenta may require additional sagittal and parasagittal scans. It is not difficult to locate the placenta except when it is on the lower
posterior wall. The overview might be difficult due to extremities or a larger presenting part of the fetus casting a shadow on the deeper portion of the image.
Scanning from the right or left side of the uterus or scanning transvaginally can
help overcome the problem.
Fig. 6.6 The placenta is located on the posterior wall, covering the internal os of the cervical
canal. The placental edge is marked with +.
117

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Fig. 6.7 The placenta is located on the posterior wall. A local contraction of the uterus
behind the placenta can clearly be distinguished, making the placenta seem to be protruding
into the amniotic fluid.
Placenta praevia
The placenta may cover the internal uterine os (see Fig. 6.6). When this is the
case, an exact delineation of the location of the placenta and a specific manage-
Ultrasound in obstetrics and gynaecology
ment protocol are required. If more than 2.5 cm of the placenta covers the internal os, it is characterized as placenta praevia. A transvaginal scan may assist in
providing a more detailed location of the lower portion of the placenta. In addition to the detailed relation to the internal os, it is important to describe the main
location of the placenta. Particular attention is required when the placenta covers
the internal os and a major part of the placenta is located in the lower anterior
portion of the uterus, which may interfere with a surgical approach to deliver the
fetus.
118
Suggested management protocol for suspected placenta praevia
Management when the placental edge related to the internal os at 18–20 weeks is:
=1 cm from internal os. No further scans. Placenta praevia is unlikely.
•
<1 cm from or <2.5 cm overlying the internal os. Repeat scan at 35 weeks
•
(or earlier in case of bleeding).
2.5 cm overlying the internal os. Most likely placenta praevia at term. Plan for
•
a caesarean section at 38 weeks following verification of placental location.
PLACENTAL MORPHOLOGY
Sometimes small sonolucent areas may be located within the regular fine-grained
texture of the placenta, usually towards the basal plate (Fig. 6.8). They are usu-
ally referred to as placental lakes and represent areas without any fetal villi which
consist of slowly moving blood. They have no clinical significance.
Placental cysts may be located close to the chorionic plate. They are superfi-
cial vessels seen in cross-section or as longitudinal tubes. They have no clinical
significance.
The placental texture changes during the course of a pregnancy. These mor-
phological changes have not been proven to have any clinical implications16 but
15

✩✩✩✩✩✩✩✩✩✩✩ ✩
Fig. 6.8 Anterior placenta with a placental lake.
it is useful to have knowledge of the described changes, which are part of the
gradual ageing process of the placenta.
Grannum, who classified them into grades 0, I, II and III, has described these
changes, called placental grading, in detail.5 Grade 0 represents the normal finegrained homogenic placenta. Grade I presents with multiple echogenic areas,
grade II has echogenic areas towards the base and comma-like indentions in the
chorionic plate. Grade III has, in addition to grade II, cystic areas within the placenta and echogenic irregular areas beneath the chorionic plate.
Amniotic fluid and placental localization
CONCLUSION
The placenta is regarded as an organ of fetal origin as it develops from the trophoblast. It is the interface between the maternal and fetal circulation. The
human placenta has approximately 120 cotyledons, each of which derives its
vascular supply from the fetus. The development of the placenta may be followed from week 8 onwards. By week 12, distinction of the placenta, with the
basal plate facing the uterus and the chorionic plate facing the fetus, is possible.
The indications for localization of the placenta are in connection with intrauterine invasive procedures, with bleeding in the second trimester, as part of the
routine second-trimester scan and prior to external version in late pregnancy.
The distinction of the relation of the inner cervical os and the placental edge is
important. A management protocol for placenta praevia must be followed.
References
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understanding the regulation of amniotic
fluid: water and solute fluxes in and
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Placenta 1995;16:1–18
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120

7
Assessment of the placenta and umbilical cord
Eric Jauniaux
ABSTRACT
With improvement of ultrasound equipment, obstetricians are now able to
examine the placenta and the cord in detail before delivery and to investigate the
placental circulations in vivo. Over the last two decades ultrasound has gained an
important role in the prenatal diagnosis and management of:
first- and second-trimester intrauterine haematomas which are associated
with premature rupture of the membranes and preterm onset of labour
placenta accreta which is characterized by myometrial invasion by villi
tissue and occurs when the decidua basalis is partially or completely
absent
vascular chorioangiomas which are associated with an increased incidence of
polyhydramnios and fetal growth retardation
complete and partial hydatidiform mole which can both be associated with
persisting gestational trophoblastic tumours
vascular placental lesions such as large thrombosis and infarcts which are
usually found during the third trimester and are associated with fetal
growth restriction
the absence of one umbilical artery which is found in association with many
fetal anatomical defects and which when isolated leads to poor fetal growth
in about 20% of the cases
abnormal cord insertion and position which can be associated with severe
obstetric complications.
These findings demonstrate that the differential diagnosis of placental and cord
abnormalities is now possible in utero and that placental examination should be
part of all routine ultrasound examinations.
KEYWORDS
Placenta, trophoblast, tumour, umbilical cord.
121

INTRODUCTION
Before the development of ultrasound imaging, morphological examination of the
placenta and the cord was only of epidemiological value and was therefore of little
influence on pregnancy management. With the advent of modern ultrasound equipment, it is now possible to examine the placenta and the cord in detail from the
beginning of the first trimester. A gestational sac of 2–3 mm can be detected as early
as 4 weeks and 1 or 2 days menstrual age. In fact, the term ‘gestational sac’ refers to
the chorionic cavity and the rim of placental villi and underlying decidual proliferation, which is the first evidence of a pregnancy.
Determining placental position in utero was one of the first aims of ultrasound examination in the 1960s. Visualization and localization of the placenta
by ultrasound became rapidly superior to all other imaging techniques such as
radiographic placentography or scintigraphy and is now an essential part of routine prenatal examinations. The ultrasound features of most placental or cord
vascular lesions may undergo major changes within a few days. When a placental
or cord abnormality, which could be associated with perinatal complications, is
Ultrasound in obstetrics and gynaecology
suspected, serial sonographic examinations should be performed.
The information which can now be obtained by high-resolution ultrasound
or Doppler techniques places additional demands on the clinician who requires
more extensive knowledge of the anatomy and physiology of the vascular circulatory changes that occur during pregnancy.
differential diagnoses and pathophysiology of the principal abnormalities of the
placenta and the umbilical cord will be presented.
1–30
In this chapter, the sonographic
122
MAJOR STRUCTURAL ABNORMALITIES OF THE PLACENTA
In describing placental lesions, ultrasonographers have used many inaccurate and
misleading expressions. This is probably due to the fact that little attempt has
been made to compare ultrasound and pathological findings. One should always
refer to the histopathological terminology to categorize these lesions and evaluate
their clinical significance.
CONGENITAL ABNORMALITIES
Abnormalities of placentation
Placenta extrachorialis
This is a common abnormality, found in about 25% of all placentas, and characterized by a transition of membranous to villous chorion at a distance from the
placental edge.9 Insertion of the membranes within the placental margin results in
placental tissue not covered by the chorionic plate (extrachorialis) and in a smaller
than normal amniotic cavity.9 Two forms can be distinguished: the circummarginate placentas and the circumvallate. Only the latter has clinical significance because
the abnormal insertion of membrane contains amnion, chorion and decidual tissue.
As the uterine wall stretches during the second half of gestation, the placenta cannot adapt and there is tearing of membranes from the edge of the chorionic plate
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