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Prof. M.C.Bansal.
MBBS;MS. FICOG. MICOG.
Founder Principal & Controller,
Jhalawar Medical college , Jalawar.
Ex.Principal&Controller;
Mahatma Gandhi Medical College,sitapura ,
Jaipur.
DR. RIDHI KATHURIA
PG 2ND year
DEPTT OF OBS & GYN
NIMS MEDICAL COLLEGE & HOSPITAL
JAIPUR
WHAT IS MEDICAL IMAGING?
MEDICAL IMAGING is the technique and process
used to create images of the human body (or parts and
function thereof) for clinical purposes (medical
procedures seeking to reveal, diagnose, or
examine disease) or medical science (including the
study of normal anatomy and physiology).
1. Ultrasonography.
2. X-Ray.
3. Hysterography.
4. Hysteroscopy.
5. CT Scan
6. MRI.
7. PET.
 Uses High-frequency broadband sound
waves.
 >20,000 Hz, i.e. 2 KHz.
 Reflected by tissues upto varying degrees
depending on the tissue content, type,
consistency.
 Receiving echoes.
 Converting the echoes into electric signals.
 Interpreting and displaying those signals
 Can be snapshot or in real time.
ULTRASONOGRAPHY
 Can be directed in a beam
Obeys the laws of reflection and refraction
Reflected by objects of quite small size
Can be converted to analogue or digital signals for image production
No radiation exposure
Non Invasive
Fast
Relatively inexpensive.
Ultrasound waves;
o Travels poorly through gas
o The amount reflected depends on the
degree of acoustic mismatch
o The piezoelectric crystals are quite delicate
The ultrasound beam & the receipt of echoes is achieved by
PIEZOELECTRIC CRYSTALS
 Mounted in an array on a probe.
 The probe can be fixed or oscillating.
 The wave of sound can be focused to a point of interest.
 The image is displayed on an oscilloscope or TV
screen.
The image will be formed by-
1) Direction of echo.
2) Strength of echo.
3) Time taken for the echo to return.
 These 3 characteristics determine which pixels on the
screen will light up & with what intensity.
DIAGNOSTICULTRASOUND a. Typically involves frequencies of 2 – 15
mHz
b. Lower frequencies will give greater
penetration
c. And thereby one can see further
d. Higher frequencies allow to see more
detail
e. But the penetration is less
f. And very high frequencies have the
potential for adverse biological effects
Hand held Probes.
Contain the Piezoelectrical
Crystals.
Of varying types depending
on shape, usage, desired
structure/area to be
visualised.
LINEAR
PROBE
A Linear Array of Crystals
Produces parallel sound waves
And a rectangular image
Good for surface structures
CURVED
PROBE
A Curved Array of Crystals
Will fit curved surfaces of the body
The density of scan decreases
proportionally to the distance from the
transducer
SECTOR
PROBE
Produces a fan-like image
Can fit into narrow spaces
Has poor near-field resolution
TRANS
VAGINAL
PROBE
A Sector Array of Crystals
Used to scan by placing it within the
vaginal opening.
More detailed view of the structures.
Special emphasis for follicular monitering.
Ultrasound is no substitute for a good history & a thorough
clinical (general & specific systemic) examination .
ALWAYS do an abdominal scan before using the vaginal
probe.
The trick is to build up a 3-dimensional picture in your
mind using real-time imaging
TRANS ABDOMINAL
 Full bladder
 Panaromic view
 For large masses
 Abdominal organs
 Lymphnodes
TRANS VAGINAL
 Empty bladder
 In gynecology diseases
 Uterus , ovaries, follicles
 Pouch of Douglas
TRANS PERINEAL
Pelvic floor muscles
TRANS RECTAL
 Pubo-Rectalis Muscle
 Anal Sphincter
NORMALAPPEARANCES
TRANSVERSE SECTION OF
THE STRUCTURES, JUST
ABOVE THE PUBIC
SYMPHYSIS.
(OVARIES SEEN CLEARLY
AS HERE, MAY NOT BE
POSSIBLE IN ALL CASES)
TRANS VAGINAL SCANNING
ANTEVERTED UTERUS:- Fundus
faces the same direction as bladder
RETROVERTED UTERUS:- Fundus faces
the opposite direction as bladder
Normal Appearance
NORMAL MEASUREMENTS
Size - 7.5 x 5.0 x 2.5cm
Length - Fundus to Cervix(7.5-8.0cm)
Depth - Antero-posterior(4.5-5.0cm)
Width - Coronal view (2.5-3.0cm)
Myometrium –
Homogenous
Hypoechogenic
Endometrium-
Changes during menstrual cycle
1-4 mm after menses
8-10 mm at ovulation(tri laminar)
When evaluating a suspected uterine mass, the practitioner
should identify the appropriate anatomical structures.
The initial step is to identify the bladder anteriorly and the
rectosigmoid posteriorly.
The position of the uterus depends on the distension of the
bladder and rectosigmoid.
The normal uterus appears sonographically as a uniform
structure.
 CONGENITAL ANOMALIES
Bicornuate uterus
Sepatate uterus
Didelphous uterus
 MYOMAS
Irregular uterine contour
Hypo/iso/hyper echoic masses
Size, number, location
 ADENOMYOSIS
Enlarged uterus
Asymmetric thickening of
myometrium
Heterogeneous echotexture
ENDOMETRIALABNORMALITIES
 ABNORMAL UTERINE BLEEDING
Polyps
Submucosal fibroid
 POSTMENOPAUSAL BLEEDING
Endo thickness- >5mm needs evaluation
 ENDOMETRIAL CANCER
Myometrial invasion
 TAMOXIFEN THERAPY
Thick endometrium
Subendometrial stromal vacuolation
 MISSING IUCD
Bright echogenic
Penetration to myometrium
Translocation to peritoneal cavity
BICORNUATE UTERUS
DIDELPHUS UTERUS
F < 2cm –
Incomplete/P
artial Septum
F > 2cm –
Complete
Septum
FIBROID UTERUS
With pregnancy a myoma can be seen
better as the anechoic amniotic fluid
provides a good window.
Also as seen, cystic ill defined areas are
suggesting ‘Red Degeneration Of
Pregnancy’.
Calcific changes may also be seen as
‘RING CALCIFICATIONS’ seen
as bright line encircling the mass
POOR VASCULARITY OF THE MASS FURTHER
CONFIRMS THE DIAGNOSIS OF A FIBROID.
SUB-MUCOUS
FIBROID
The fibroid impinges
within the uterine
cavity.
SUB SEROSAL
FIBROID
The fibroid stalk may
twist on itself.
Get detached from
the original area of
attachment.
Hence, becoming a
WANDERING
FIBROID.
LIPOLEIOMYOMA
Brightness is due the fat (fatty
degeneration) content of the mass.
A common benign condition
that often co-exists with
endometriosis and fibroids,
often described as endometriosis
within the uterus itself .
Endometrial tissue exists within
the muscle of the uterus. During
menstruation this degenerates
and the blood cannot escape the
uterine muscle causing pain;
some blood may finally escape
resulting in abnormal p.v.
spotting
• MAY BE NORMAL
• Diffuse uterine enlargement with no alteration in echo-
texture or uterine contour, often reported as a “bulky
uterus”
• Asymmetrically thickened uterus, usually posteriorly
• Poorly defined focal area of hypoechoic or hyperechoic
texture within the myometrium, representing a focal
adenomyoma (can be multiple)
• Cystic hyperplasia of the endometrium
• Myometrial cysts
DIFFUSE ADENOMYOSIS
The loss of endometrial myometrial
junction when seen on images is
characteristic.
Cystic appearance with
thickened endometrium
• Deposition of calcium in
abnormal tissues, without
abnormal blood calcium levels.
• It may occur as a part of ageing
process, or may follow an
instrumentation or procedure like
curettage
• Bright echogenic lesion with
posterior shadowing is suggestive
of calcification.
• The shadowing is due to complete
reflection of the waves when they strike the
lesion.
IUCD PENETRATING THE
MYOMETRIAL WALL
Normal fallopian tubes
not seen, in a routine
scan.
Pathological tubes seen
as dilated, truncated
structures.
• PID
• Tuberculosis
• Chlamydia/Gonorrhoea
infection
• Traumatic
• Cryptomenorrhoea
• Ectopic Pregnancy
• Tubal Carcinoma
• Endometriosis
Ciliae of the inner lining (endosalpinx) of the fallopian tube
beat towards the uterus, tubal fluid is normally discharged
via the fimbriated end into the peritoneal cavity from
where it is cleared.
If the fimbriated end of the tube becomes agglutinated, the
resulting obstruction does not allow the tubal fluid to pass;
it accumulates and reverts its flow downstream, into the
uterus, or production is curtailed by damage to the
endosalpinx.
TUBAL PHIMOSIS refers to a
situation where the tubal end is
partially occluded, in this case
fertility is impeded, and the risk
of an ectopic pregnancy is
increased.
Thick
echogenic
homogenous
material
filling the
lumen is s/o
blood
Echogenic debris seen within the lumen is s/o pus.
NORMAL APPEARANCE
Position
The normal ovary in the resting (menstrual) phase is moderately
echogenic, well marginated and located at the lateral edge of the
broad ligament.
Because it is mobile, it may be found from the pelvic cul-de-sac to
the lower abdomen ( often displaced superiorly by distended
urinary bladder, coming to lie anterior and lateral to the iliac
vessels).
Despite this variability, it is typically found lateral to the fundus of
the uterus.
PREMENARCHAL (Vol. = 0-8 ml)
Ovaries are small, and often show a uniform moderately echogenic solid structure.
It is typical to note scattered antral follicles (small 3-6 mm cysts) during the years 9-13
preceding menarche.
Follicles in younger patients however are not necessarily evidence of endocrine
dysfunction.
Size of premenarchal ovaries is quite variable, making conclusions based on size
alone unreliable.
PUBERTY THROUGH MIDDLE AGE (Vol. = 0-18 ml)
Solid background with scattered antral follicles (3-6 mm cysts).
This pattern is punctuated by the regular cyclic development of graafian follicles.
POST-MENOPAUSAL (Vol. = 0-8 ml)
Solid background, antral follicles may persist 4 -5 years following clinical menopause.
Ovarian size is smaller.
Uterus Cervix & Vagina
Endometrium
Small Multifollicular Ovary Unilocular Ovary
1. Because of the ovary has a variable, usually oval shape,
size is best expressed as an estimated volume.
Volume (ml.) = Length (cm) x Width (cm) x Depth (cm) x 0.52
2. The Ratio of larger to smaller ovary should normally be
less then 2:1.
Age (yrs) Volume (ml) Mean (ml)
0-10 0.2 - 4.9 1.7
11-20 1.7 - 18.5 7.8
21-30 2.6 - 23.0 10.2
31-40 2.6 - 20.7 9.5
41-50 2.1 - 20.9 9.0
51-60 1.6 - 14.2 6.2
61-70 1.0 - 15.0 6.0
Values ; 95% confidence level
Introduction:
• Although the hormonal background of follicular development is among the
more complex endocrine events, the resulting sequence of gross
morphologic changes visualized by ultrasound is a simple sequence of
enlarging cysts.
• Using measures of size, number, and temporal progression, ultrasound can
verify normal sequences, or in many cases, diagnose ovulation failure by
recording at what point follicular development is arrested.
Normal Development:
• The resting ovary contain a women's full complement of potential follicles.
• The resting primordial follicles are too small to be seen grossly or on a scan.
Follicular
Phase
Initial follicular development occurs
during the proliferative (follicular)
phase of the menstrual cycle,
approximately days 1-14 counting from
the first day of menstrual flow, and
ends with ovulation.
During the follicular phase, a small
subset of the primordial follicles are
stimulated to develop, and
accumulate follicular fluid, with
enlargement ultimately visible by
ultrasound.
Developing Follicles are
first seen by ultrasound
as a group of 4-8 antral
follicles 3-5mm size by
day 6-7 .
By Ultrasound, early antral follicles are 2-4mm in size. Developing
follicles range between 5-10 mm.
The dominant (selected) follicle will continue to grow, reaching
10mm on day 8-9 and reaching final mature size of 18-24 mm, on day
14 prior to ovulation.
Typically subordinate (non-dominant follicles) reach 10 mm and then
become atretic.
Follicles 11 mm or larger are
usually dominate follicles.
Secretory (Luteal) Phase
On about day 14, the mature follicle expels
the oocyte.
In most cases, loss of fluid associated with
expulsion of the oocyte results in
disappearance or substantial decrease in
size of the mature follicle.
This abrupt change in size represents the
Ultrasound sign of ovulation.
Free Fluid seen in POD, is also arbitrarily
taken as a sign of ovulation
In the 1st scan, the star marked follicle is the selected
dominant follicle.
It is seen approaching the margin of the ovarian cortex
& also is the largest of all others.
The defect in the follicle heals in 2-5 days.
The wall thickens as cells are "luteinized"( lining cells enlarge and fill with lipid),
and in most cases, the antrum fills with blood to form a "Corpus Hemorrhagicum”.
The follicle becomes a "Corpus Luteum", contributing hormone secretion,
particularly progesterone to support the Secretory Phase.
On ultrasound, the corpus luteum reappears in in several forms.
• 1/3 are a typical cyst of similar size to the mature follicle or larger.
• 1/3 are more echogenic, forming a nearly "solid" ultrasound appearance.
• 1/3 are not apparent at ultrasound examination.
If pregnancy occurs, HCG secreted by the trophoblast maintains the
corpus luteum through the 10 week of gestation.
If pregnancy does not occur, the Corpus Luteum usually disappears
within a day or two of the onset of menses.
Because almost all functional ovarian cysts disappear by
the 5th day of the subsequent cycle, concerns regarding
neoplastic origin of unusually large functional of cysts
can usually be dispelled by demonstrating their
disappearance by 3-5 days into the next cycle.
For the same reason, screening for early
ovarian tumors must be done during the first 5
days of the cycle to avoid needless confusion
with physiologic cysts.
Sporadic Anovulatory
Mechanisms
Chronic Ovulation Failure
•FOLLICULAR ATRESIA
•EMPTY FOLLICLE
SYNDROME
•LEUTINIZED UNRUPTURED
FOLLICLE SYNDROME
• HYPER-GONADOTROPISM
• HYPO-GONADOTROPISM
• POLY CYSTIC OVARIAN
DISEASE/SYNDROME
FOLLICULAR ATRESIA
In these cycles, the proliferative
maturing effects of E2 (estrogen)
are not properly synchronized
with the the LH (luteinizing
hormone).
The resulting follicle does not
reach full size or ovulate.
Ultrasound shows a dominate
follicle which does not reach full
mature size (16-24mm.) and
become rapidly
atresic. This is the morphologic
pattern most frequently observed
in patients taking oral
contraceptives.
EMPTY FOLLICLE
SYNDROME
Follicular development is
grossly normal, but aspiration
or natural ovulation does not
produce an oocyte.
Failure to demonstrate a
cumulus oophorus with a
mature follicle on very high
resolution ultrasound may be
seen.
However visualization of the
cumulus is difficult under
optimal conditions, the
accuracy of ultrasound
in demonstrating the
syndrome in probably low.
Under routine study, these
cycles are likely to appear
normal.
LEUTINIZED
UNRUPTURED FOLLICLE
SYNDROME
In this syndrome, an
apparently normal mature
luteinized follicle fails to
rupture and ovulate. It
goes on to behave as a
luteinized follicle.
The syndrome can be
recognized as a follicle
which fails to collapse in
association with the
expected LH peak.
Ultrasound findings cant
be taken as conclusive.
HYPER-GONADOTROPISM
Primary ovarian failure leads to small
ovaries and low secretion of estrogen.
The anestrogenic state leads
to lack of feedback on gonadotrophin
secretion and Hypergonadotropism.
Causes include primary failure,
autoimmune damage, and chromosomal
mosaicism.
Ultrasound shows small or absent
ovaries without follicles.
Except in autoimmune causes, this
group of patients do not respond to
treatment.
HYPO-GONADOTROPISM
FSH and LH levels are found to be low,
and evaluation for pituitary tumor is
indicated.
Ovarian function is often normal and
may be recovered through correction of
pituitary problems, or exogenous FSH
and HCG (LH replacement).
Due to inadequate stimulation, these
patients also have low
estrogen levels.
On ultrasound, these patients
ovaries may be "normal", but
are more often enlarged
( > 6ml), and tend to have an
increased number of small
incompletely developed
follicles (>11) and no
dominant size follicles.
The stroma in the central part
of the ovary is usually
abundant and hyperechoic.
Doppler blood flow has been
reported to be faster in PCOS.
• May show features of polycystic ovaries
– Bilateral enlarged ovaries with multiple small follicles : 50%
• Increased ovarian size (> 10 cc)
• 12 or more follicles measuring 2 - 9 mm
• Follicles of similar size
• Peripheral location of follicles : which can give a String Of Pearl
Appearance
• Hyperechoic central stroma
• Ovarian outline may be slightly irregular
• Hypo-echoic ovary without individual cysts : 25%
• Normal ovaries : 25%
• Endometrium – may appear as proliferative
Ovarian
Hyperstimulation
Syndrome (OHSS)
is a complication
from some forms
of fertility
medication.
Ovarian hyperstimulation syndrome is particularly associated with injection of a
hormone called human chorionic gonadotropin (hCG) which is used for inducing
final oocyte maturation and/or triggering oocyte release.
The risk is further increased by multiple doses of hCG after ovulation and if the
procedure results in pregnancy.
Using a GnRH agonist instead of hCG for inducing final oocyte maturation and/or
release results in an elimination of the risk of ovarian hyperstimulation syndrome,
but a slight decrease of the delivery rate of approximately 6%
Based upon the clinical manifestation and imaging findings, OHSS
can be classified into
• Mild OHSS : Characterised by bilateral multicystic ovarian
enlargement;
• Moderate OHSS : If there is associated ascites and abdominal
distension;
• Severe OHSS : Characterised by hypovolemia,
haemoconcentration, thrombosis, oliguria, pleural and
pericardial effusion.
Typically shows bilateral
symmetric enlargement of
ovaries (often > 12 cm) with
multiple cysts of varying sizes,
giving the classic
WHEEL - SPOKE
APPEARANCE.
Associated ascites, pleural + /
pericardial effusion (which is
due to capillary leak) may also
be present.
• Ultrasound is the preferred imaging
modality. Typically an ovarian dermoid is
seen as a cystic adnexal mass with some
mural components. Most lesions are
unilocular.
• Rokintansky Nodule / Dermoid Plug
• Diffusely or partially echogenic mass with
posterior attenuation owing to sebaceous
material and hair within the cyst cavity : TIP
OF THE ICEBERG Sign
• Echogenic, shadowing calcific or dental
(tooth) components
• Presence of fluid-fluid levels
• Multiple thin, echogenic bands caused by
hair in the cyst cavity : DOT & DASH
PATTERN.
Sebaceous material/hair/
calcified material within the
cyst.
Acoustic mismatch
Attenuation of the rays
passing through the above
contents.
Behind these structures, all
appears dark (sono-opaque)
Rokitansky nodule or Dermoid plug refers to a
solid protuberence projecting from an ovarian
cyst in the context of a mature teratoma.
It often contains calcific, dental, adipose, hair
and / or sebaceous components
• A Theca Lutein Cyst is a type of
bilateral functional ovarian cyst filled
with clear, straw-colored fluid.
• To be classified a functional cyst, the
mass must reach a diameter of at least
three centimeters.
• These cysts originate when abnromally
high Beta-HCG are elevated, which can
occur due to multifetal gestations or
molar pregnancies.
B/L THECA CYSTS
CORPUS LUTEAL (CL) cyst is a
type of functional ovarian cyst which
results when a corpus luteum fails to
regress following the release of
an ovum.
Such a cyst is complicated further by
hemorrhage occurring within the cyst.
When associated with pregnancy, it
is the most common pelvic mass
encountered within the
1st trimester.
Colour Doppler shows either no vascularity
within the cyst or at times show low resistance
blood flow around the cyst
Ectopic Endometrium
when present within
the ovaries, proliferates
under the influence of
hormones, during the
normal cycles.
Seen here, is the
classical GROUND
GLASS
APPEARANCE
Transabdominal ultrasound shows a
multiloculated right ovarian endometrioma
with low level echoes
Imaging in obstetrics & gynaecology (part 1- Gynaecological scans in benign conditions)

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Imaging in obstetrics & gynaecology (part 1- Gynaecological scans in benign conditions)

  • 1. Prof. M.C.Bansal. MBBS;MS. FICOG. MICOG. Founder Principal & Controller, Jhalawar Medical college , Jalawar. Ex.Principal&Controller; Mahatma Gandhi Medical College,sitapura , Jaipur. DR. RIDHI KATHURIA PG 2ND year DEPTT OF OBS & GYN NIMS MEDICAL COLLEGE & HOSPITAL JAIPUR
  • 2. WHAT IS MEDICAL IMAGING? MEDICAL IMAGING is the technique and process used to create images of the human body (or parts and function thereof) for clinical purposes (medical procedures seeking to reveal, diagnose, or examine disease) or medical science (including the study of normal anatomy and physiology).
  • 3. 1. Ultrasonography. 2. X-Ray. 3. Hysterography. 4. Hysteroscopy. 5. CT Scan 6. MRI. 7. PET.
  • 4.  Uses High-frequency broadband sound waves.  >20,000 Hz, i.e. 2 KHz.  Reflected by tissues upto varying degrees depending on the tissue content, type, consistency.  Receiving echoes.  Converting the echoes into electric signals.  Interpreting and displaying those signals  Can be snapshot or in real time. ULTRASONOGRAPHY
  • 5.  Can be directed in a beam Obeys the laws of reflection and refraction Reflected by objects of quite small size Can be converted to analogue or digital signals for image production No radiation exposure Non Invasive Fast Relatively inexpensive.
  • 6. Ultrasound waves; o Travels poorly through gas o The amount reflected depends on the degree of acoustic mismatch o The piezoelectric crystals are quite delicate
  • 7. The ultrasound beam & the receipt of echoes is achieved by PIEZOELECTRIC CRYSTALS  Mounted in an array on a probe.  The probe can be fixed or oscillating.  The wave of sound can be focused to a point of interest.  The image is displayed on an oscilloscope or TV screen. The image will be formed by- 1) Direction of echo. 2) Strength of echo. 3) Time taken for the echo to return.  These 3 characteristics determine which pixels on the screen will light up & with what intensity.
  • 8. DIAGNOSTICULTRASOUND a. Typically involves frequencies of 2 – 15 mHz b. Lower frequencies will give greater penetration c. And thereby one can see further d. Higher frequencies allow to see more detail e. But the penetration is less f. And very high frequencies have the potential for adverse biological effects
  • 9. Hand held Probes. Contain the Piezoelectrical Crystals. Of varying types depending on shape, usage, desired structure/area to be visualised.
  • 10.
  • 11. LINEAR PROBE A Linear Array of Crystals Produces parallel sound waves And a rectangular image Good for surface structures
  • 12. CURVED PROBE A Curved Array of Crystals Will fit curved surfaces of the body The density of scan decreases proportionally to the distance from the transducer
  • 13. SECTOR PROBE Produces a fan-like image Can fit into narrow spaces Has poor near-field resolution
  • 14. TRANS VAGINAL PROBE A Sector Array of Crystals Used to scan by placing it within the vaginal opening. More detailed view of the structures. Special emphasis for follicular monitering.
  • 15.
  • 16. Ultrasound is no substitute for a good history & a thorough clinical (general & specific systemic) examination . ALWAYS do an abdominal scan before using the vaginal probe. The trick is to build up a 3-dimensional picture in your mind using real-time imaging
  • 17. TRANS ABDOMINAL  Full bladder  Panaromic view  For large masses  Abdominal organs  Lymphnodes TRANS VAGINAL  Empty bladder  In gynecology diseases  Uterus , ovaries, follicles  Pouch of Douglas TRANS PERINEAL Pelvic floor muscles TRANS RECTAL  Pubo-Rectalis Muscle  Anal Sphincter
  • 18. NORMALAPPEARANCES TRANSVERSE SECTION OF THE STRUCTURES, JUST ABOVE THE PUBIC SYMPHYSIS. (OVARIES SEEN CLEARLY AS HERE, MAY NOT BE POSSIBLE IN ALL CASES)
  • 19.
  • 20. TRANS VAGINAL SCANNING ANTEVERTED UTERUS:- Fundus faces the same direction as bladder RETROVERTED UTERUS:- Fundus faces the opposite direction as bladder
  • 21.
  • 22.
  • 24. NORMAL MEASUREMENTS Size - 7.5 x 5.0 x 2.5cm Length - Fundus to Cervix(7.5-8.0cm) Depth - Antero-posterior(4.5-5.0cm) Width - Coronal view (2.5-3.0cm) Myometrium – Homogenous Hypoechogenic Endometrium- Changes during menstrual cycle 1-4 mm after menses 8-10 mm at ovulation(tri laminar)
  • 25. When evaluating a suspected uterine mass, the practitioner should identify the appropriate anatomical structures. The initial step is to identify the bladder anteriorly and the rectosigmoid posteriorly. The position of the uterus depends on the distension of the bladder and rectosigmoid. The normal uterus appears sonographically as a uniform structure.
  • 26.  CONGENITAL ANOMALIES Bicornuate uterus Sepatate uterus Didelphous uterus  MYOMAS Irregular uterine contour Hypo/iso/hyper echoic masses Size, number, location  ADENOMYOSIS Enlarged uterus Asymmetric thickening of myometrium Heterogeneous echotexture
  • 27. ENDOMETRIALABNORMALITIES  ABNORMAL UTERINE BLEEDING Polyps Submucosal fibroid  POSTMENOPAUSAL BLEEDING Endo thickness- >5mm needs evaluation  ENDOMETRIAL CANCER Myometrial invasion  TAMOXIFEN THERAPY Thick endometrium Subendometrial stromal vacuolation  MISSING IUCD Bright echogenic Penetration to myometrium Translocation to peritoneal cavity
  • 28.
  • 31. F < 2cm – Incomplete/P artial Septum F > 2cm – Complete Septum
  • 33.
  • 34. With pregnancy a myoma can be seen better as the anechoic amniotic fluid provides a good window. Also as seen, cystic ill defined areas are suggesting ‘Red Degeneration Of Pregnancy’. Calcific changes may also be seen as ‘RING CALCIFICATIONS’ seen as bright line encircling the mass
  • 35. POOR VASCULARITY OF THE MASS FURTHER CONFIRMS THE DIAGNOSIS OF A FIBROID.
  • 38. The fibroid stalk may twist on itself. Get detached from the original area of attachment. Hence, becoming a WANDERING FIBROID.
  • 39. LIPOLEIOMYOMA Brightness is due the fat (fatty degeneration) content of the mass.
  • 40. A common benign condition that often co-exists with endometriosis and fibroids, often described as endometriosis within the uterus itself . Endometrial tissue exists within the muscle of the uterus. During menstruation this degenerates and the blood cannot escape the uterine muscle causing pain; some blood may finally escape resulting in abnormal p.v. spotting
  • 41. • MAY BE NORMAL • Diffuse uterine enlargement with no alteration in echo- texture or uterine contour, often reported as a “bulky uterus” • Asymmetrically thickened uterus, usually posteriorly • Poorly defined focal area of hypoechoic or hyperechoic texture within the myometrium, representing a focal adenomyoma (can be multiple) • Cystic hyperplasia of the endometrium • Myometrial cysts
  • 42. DIFFUSE ADENOMYOSIS The loss of endometrial myometrial junction when seen on images is characteristic. Cystic appearance with thickened endometrium
  • 43.
  • 44. • Deposition of calcium in abnormal tissues, without abnormal blood calcium levels. • It may occur as a part of ageing process, or may follow an instrumentation or procedure like curettage • Bright echogenic lesion with posterior shadowing is suggestive of calcification. • The shadowing is due to complete reflection of the waves when they strike the lesion.
  • 45.
  • 46.
  • 47.
  • 49.
  • 50.
  • 51.
  • 52. Normal fallopian tubes not seen, in a routine scan. Pathological tubes seen as dilated, truncated structures.
  • 53. • PID • Tuberculosis • Chlamydia/Gonorrhoea infection • Traumatic • Cryptomenorrhoea • Ectopic Pregnancy • Tubal Carcinoma • Endometriosis Ciliae of the inner lining (endosalpinx) of the fallopian tube beat towards the uterus, tubal fluid is normally discharged via the fimbriated end into the peritoneal cavity from where it is cleared. If the fimbriated end of the tube becomes agglutinated, the resulting obstruction does not allow the tubal fluid to pass; it accumulates and reverts its flow downstream, into the uterus, or production is curtailed by damage to the endosalpinx.
  • 54. TUBAL PHIMOSIS refers to a situation where the tubal end is partially occluded, in this case fertility is impeded, and the risk of an ectopic pregnancy is increased.
  • 55.
  • 56.
  • 58. Echogenic debris seen within the lumen is s/o pus.
  • 59.
  • 61. Position The normal ovary in the resting (menstrual) phase is moderately echogenic, well marginated and located at the lateral edge of the broad ligament. Because it is mobile, it may be found from the pelvic cul-de-sac to the lower abdomen ( often displaced superiorly by distended urinary bladder, coming to lie anterior and lateral to the iliac vessels). Despite this variability, it is typically found lateral to the fundus of the uterus.
  • 62. PREMENARCHAL (Vol. = 0-8 ml) Ovaries are small, and often show a uniform moderately echogenic solid structure. It is typical to note scattered antral follicles (small 3-6 mm cysts) during the years 9-13 preceding menarche. Follicles in younger patients however are not necessarily evidence of endocrine dysfunction. Size of premenarchal ovaries is quite variable, making conclusions based on size alone unreliable. PUBERTY THROUGH MIDDLE AGE (Vol. = 0-18 ml) Solid background with scattered antral follicles (3-6 mm cysts). This pattern is punctuated by the regular cyclic development of graafian follicles. POST-MENOPAUSAL (Vol. = 0-8 ml) Solid background, antral follicles may persist 4 -5 years following clinical menopause. Ovarian size is smaller.
  • 63. Uterus Cervix & Vagina Endometrium
  • 64. Small Multifollicular Ovary Unilocular Ovary
  • 65.
  • 66. 1. Because of the ovary has a variable, usually oval shape, size is best expressed as an estimated volume. Volume (ml.) = Length (cm) x Width (cm) x Depth (cm) x 0.52 2. The Ratio of larger to smaller ovary should normally be less then 2:1. Age (yrs) Volume (ml) Mean (ml) 0-10 0.2 - 4.9 1.7 11-20 1.7 - 18.5 7.8 21-30 2.6 - 23.0 10.2 31-40 2.6 - 20.7 9.5 41-50 2.1 - 20.9 9.0 51-60 1.6 - 14.2 6.2 61-70 1.0 - 15.0 6.0 Values ; 95% confidence level
  • 67. Introduction: • Although the hormonal background of follicular development is among the more complex endocrine events, the resulting sequence of gross morphologic changes visualized by ultrasound is a simple sequence of enlarging cysts. • Using measures of size, number, and temporal progression, ultrasound can verify normal sequences, or in many cases, diagnose ovulation failure by recording at what point follicular development is arrested.
  • 68. Normal Development: • The resting ovary contain a women's full complement of potential follicles. • The resting primordial follicles are too small to be seen grossly or on a scan.
  • 69. Follicular Phase Initial follicular development occurs during the proliferative (follicular) phase of the menstrual cycle, approximately days 1-14 counting from the first day of menstrual flow, and ends with ovulation. During the follicular phase, a small subset of the primordial follicles are stimulated to develop, and accumulate follicular fluid, with enlargement ultimately visible by ultrasound. Developing Follicles are first seen by ultrasound as a group of 4-8 antral follicles 3-5mm size by day 6-7 .
  • 70. By Ultrasound, early antral follicles are 2-4mm in size. Developing follicles range between 5-10 mm. The dominant (selected) follicle will continue to grow, reaching 10mm on day 8-9 and reaching final mature size of 18-24 mm, on day 14 prior to ovulation. Typically subordinate (non-dominant follicles) reach 10 mm and then become atretic. Follicles 11 mm or larger are usually dominate follicles.
  • 71. Secretory (Luteal) Phase On about day 14, the mature follicle expels the oocyte. In most cases, loss of fluid associated with expulsion of the oocyte results in disappearance or substantial decrease in size of the mature follicle. This abrupt change in size represents the Ultrasound sign of ovulation. Free Fluid seen in POD, is also arbitrarily taken as a sign of ovulation In the 1st scan, the star marked follicle is the selected dominant follicle. It is seen approaching the margin of the ovarian cortex & also is the largest of all others.
  • 72. The defect in the follicle heals in 2-5 days. The wall thickens as cells are "luteinized"( lining cells enlarge and fill with lipid), and in most cases, the antrum fills with blood to form a "Corpus Hemorrhagicum”. The follicle becomes a "Corpus Luteum", contributing hormone secretion, particularly progesterone to support the Secretory Phase. On ultrasound, the corpus luteum reappears in in several forms. • 1/3 are a typical cyst of similar size to the mature follicle or larger. • 1/3 are more echogenic, forming a nearly "solid" ultrasound appearance. • 1/3 are not apparent at ultrasound examination. If pregnancy occurs, HCG secreted by the trophoblast maintains the corpus luteum through the 10 week of gestation. If pregnancy does not occur, the Corpus Luteum usually disappears within a day or two of the onset of menses.
  • 73. Because almost all functional ovarian cysts disappear by the 5th day of the subsequent cycle, concerns regarding neoplastic origin of unusually large functional of cysts can usually be dispelled by demonstrating their disappearance by 3-5 days into the next cycle. For the same reason, screening for early ovarian tumors must be done during the first 5 days of the cycle to avoid needless confusion with physiologic cysts.
  • 74. Sporadic Anovulatory Mechanisms Chronic Ovulation Failure •FOLLICULAR ATRESIA •EMPTY FOLLICLE SYNDROME •LEUTINIZED UNRUPTURED FOLLICLE SYNDROME • HYPER-GONADOTROPISM • HYPO-GONADOTROPISM • POLY CYSTIC OVARIAN DISEASE/SYNDROME
  • 75. FOLLICULAR ATRESIA In these cycles, the proliferative maturing effects of E2 (estrogen) are not properly synchronized with the the LH (luteinizing hormone). The resulting follicle does not reach full size or ovulate. Ultrasound shows a dominate follicle which does not reach full mature size (16-24mm.) and become rapidly atresic. This is the morphologic pattern most frequently observed in patients taking oral contraceptives. EMPTY FOLLICLE SYNDROME Follicular development is grossly normal, but aspiration or natural ovulation does not produce an oocyte. Failure to demonstrate a cumulus oophorus with a mature follicle on very high resolution ultrasound may be seen. However visualization of the cumulus is difficult under optimal conditions, the accuracy of ultrasound in demonstrating the syndrome in probably low. Under routine study, these cycles are likely to appear normal. LEUTINIZED UNRUPTURED FOLLICLE SYNDROME In this syndrome, an apparently normal mature luteinized follicle fails to rupture and ovulate. It goes on to behave as a luteinized follicle. The syndrome can be recognized as a follicle which fails to collapse in association with the expected LH peak. Ultrasound findings cant be taken as conclusive.
  • 76. HYPER-GONADOTROPISM Primary ovarian failure leads to small ovaries and low secretion of estrogen. The anestrogenic state leads to lack of feedback on gonadotrophin secretion and Hypergonadotropism. Causes include primary failure, autoimmune damage, and chromosomal mosaicism. Ultrasound shows small or absent ovaries without follicles. Except in autoimmune causes, this group of patients do not respond to treatment. HYPO-GONADOTROPISM FSH and LH levels are found to be low, and evaluation for pituitary tumor is indicated. Ovarian function is often normal and may be recovered through correction of pituitary problems, or exogenous FSH and HCG (LH replacement). Due to inadequate stimulation, these patients also have low estrogen levels.
  • 77. On ultrasound, these patients ovaries may be "normal", but are more often enlarged ( > 6ml), and tend to have an increased number of small incompletely developed follicles (>11) and no dominant size follicles. The stroma in the central part of the ovary is usually abundant and hyperechoic. Doppler blood flow has been reported to be faster in PCOS.
  • 78.
  • 79.
  • 80.
  • 81. • May show features of polycystic ovaries – Bilateral enlarged ovaries with multiple small follicles : 50% • Increased ovarian size (> 10 cc) • 12 or more follicles measuring 2 - 9 mm • Follicles of similar size • Peripheral location of follicles : which can give a String Of Pearl Appearance • Hyperechoic central stroma • Ovarian outline may be slightly irregular • Hypo-echoic ovary without individual cysts : 25% • Normal ovaries : 25% • Endometrium – may appear as proliferative
  • 82. Ovarian Hyperstimulation Syndrome (OHSS) is a complication from some forms of fertility medication.
  • 83. Ovarian hyperstimulation syndrome is particularly associated with injection of a hormone called human chorionic gonadotropin (hCG) which is used for inducing final oocyte maturation and/or triggering oocyte release. The risk is further increased by multiple doses of hCG after ovulation and if the procedure results in pregnancy. Using a GnRH agonist instead of hCG for inducing final oocyte maturation and/or release results in an elimination of the risk of ovarian hyperstimulation syndrome, but a slight decrease of the delivery rate of approximately 6%
  • 84. Based upon the clinical manifestation and imaging findings, OHSS can be classified into • Mild OHSS : Characterised by bilateral multicystic ovarian enlargement; • Moderate OHSS : If there is associated ascites and abdominal distension; • Severe OHSS : Characterised by hypovolemia, haemoconcentration, thrombosis, oliguria, pleural and pericardial effusion.
  • 85. Typically shows bilateral symmetric enlargement of ovaries (often > 12 cm) with multiple cysts of varying sizes, giving the classic WHEEL - SPOKE APPEARANCE. Associated ascites, pleural + / pericardial effusion (which is due to capillary leak) may also be present.
  • 86.
  • 87. • Ultrasound is the preferred imaging modality. Typically an ovarian dermoid is seen as a cystic adnexal mass with some mural components. Most lesions are unilocular. • Rokintansky Nodule / Dermoid Plug • Diffusely or partially echogenic mass with posterior attenuation owing to sebaceous material and hair within the cyst cavity : TIP OF THE ICEBERG Sign • Echogenic, shadowing calcific or dental (tooth) components • Presence of fluid-fluid levels • Multiple thin, echogenic bands caused by hair in the cyst cavity : DOT & DASH PATTERN.
  • 88. Sebaceous material/hair/ calcified material within the cyst. Acoustic mismatch Attenuation of the rays passing through the above contents. Behind these structures, all appears dark (sono-opaque)
  • 89. Rokitansky nodule or Dermoid plug refers to a solid protuberence projecting from an ovarian cyst in the context of a mature teratoma. It often contains calcific, dental, adipose, hair and / or sebaceous components
  • 90. • A Theca Lutein Cyst is a type of bilateral functional ovarian cyst filled with clear, straw-colored fluid. • To be classified a functional cyst, the mass must reach a diameter of at least three centimeters. • These cysts originate when abnromally high Beta-HCG are elevated, which can occur due to multifetal gestations or molar pregnancies.
  • 92. CORPUS LUTEAL (CL) cyst is a type of functional ovarian cyst which results when a corpus luteum fails to regress following the release of an ovum. Such a cyst is complicated further by hemorrhage occurring within the cyst. When associated with pregnancy, it is the most common pelvic mass encountered within the 1st trimester.
  • 93. Colour Doppler shows either no vascularity within the cyst or at times show low resistance blood flow around the cyst
  • 94. Ectopic Endometrium when present within the ovaries, proliferates under the influence of hormones, during the normal cycles. Seen here, is the classical GROUND GLASS APPEARANCE
  • 95. Transabdominal ultrasound shows a multiloculated right ovarian endometrioma with low level echoes

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