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Case Presentation: Partial molar Pregnancy

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Title: Case Presentation: Partial molar Pregnancy


1
Case Presentation Partial molar Pregnancy
  • Dr Haseena Hamdani
  • Avicenna Medical Centre

2
Introduction
  • Case Report of Partial molar pregnancy.
  • Brief discussion about partial molar pregnancy.
  • Role of Diagnostics in Management.

3
Case Report
  • Asian woman
  • 27years old
  • Nulliparous
  • Consanguineous marriage
  • Combined oral pills for puberty menorrhagia

4
First visit
  • Presenting Symptoms
  • Amenorrhoea 6 weeks
  • Clinical Examination
  • Urine pregnancy test positive
  • PV examination Bulky soft uterus

5
Follow up visit after 4 weeks
  • Presenting Symptoms
  • Amenorrhea 10 weeks
  • Abdominal USG-
  • Gestational sac present.
  • Ill defined fetal echo present.
  • Cardiac pulsation not seen.
  • Few small cisterns in part of placenta

6
Second follow up visit after three days
  • Serum Beta HCG levels-
  • 125,000mIU/ ml,
  • 138,000mIU/ml after 48 hrs.
  • Repeat USG
  • Same findings

7
Second follow up visit
  • Clinical impression
  • ? Partial mole
  • Plan
  • suction evacuation followed by histological
    analysis.
  • Follow up by serum HCG estimation.

8
Treatment
  • Suction Evacuation done.
  • Curetted material sent for Histo-pathology.

9
Histo-pathology report
  • Findings
  • Fetal tissue with fetal vessels present.
  • Hydropic degeneration of chorionic villi
  • Trophoblastic hyperplasia seen at few places.
  • Conclusion
  • ? Missed abortion with hydropic degeneration of
    placenta
  • ? Partial mole ( Correlate clinically).
  • Advice serum HCG level after 4 weeks

10
Post-evacuation follow up
  • Irregular scanty bleeding P/V for 3weeks
  • HCG levels
  • After 4 weeks-543mIU/ml
  • After 6 weeks- 58.73mIU/ml
  • After 8 weeks- 11.67mIU/ml
  • After 10 weeks- 3.16mIU/ml

11
Post-evacuation follow up
  • Advice
  • use combined oral pills for next 6 months,
  • follow up for HCG levels every month for 6
    months.

12
Brief Discussion
  • Gestational trophoblastic Diseases.
  • Molar pregnancy
  • Complete molar pregnancy
  • Partial molar Pregnancy
  • Invasive Mole
  • Chorio-carcinoma
  • Placental-site trophoblastic tumor

13
Characteristics of GTD
  • Arise from fetal chorion
  • Secrete HCG
  • Good response to chemotherapy
  • Variable Malignant Potential

14
Gestational Trophoblastic Diseases
  • Incidence
  • Asians 1 in 200- 300
  • Africans 1 in 800
  • Caucasians 1 in 2000
  • Maximum in Indonesia, Japan, and Philippine

15
Predisposing factors
  • Race
  • Deficiency of Protein or carotene
  • Age- Higher towards the beginning, or end of
    childbearing age.
  • HLA-B locus antigen compatibility with Husband
  • Smoking
  • Oral contraceptives for more than 5years
  • H/O infertility

16
Partial Mole
  • Differs from Complete mole
  • Morphology
  • Clinical picture
  • Pathogenesis
  • Genetics
  • Synonyms-Triploidy, partial hydatidiform mole,
    partial molar pregnancy.
  • Undiagnosed
  • Unreported

17
  • Partial Mole is common, but unawared,
    underdiagnosed, and underreported.

18
Importance of Diagnosis
  • 4-12 develop in persistent gestational
    trophoblastic diseases, and require chemotherapy.
  • Recurrence -3
  • Chorio-carcinoma-1

19
Pathogenesis
  • Two sperms fertilize a single ovum,
  • Development of certain or all fetal parts
  • Triploid karyotype of 69XXX, 69XXY, OR 69XYY.
  • Diploid or tetraploid karyotype may exist.

20
Pathogenesis
69xxx
69xxy
46xxy
69xyy
21
Diagnostics in management
  • Tumor markers
  • Serum HCG
  • Alpha feto-protein.
  • Others like PAPP, Pregnancy specific protein,
    CA125
  • Ultrasound examination.
  • Histo-pathological Analysis.
  • Genetic Karyotyping, Flow cytometry, ploidy
    analysis etc.

22
Diagnostic Challenges
  • Clinical presentation is like normal pregnancy
    before 12 weeks.
  • HCG levels may be normal or slightly raised.
  • USG is usually confusing, specially in first
    trimester.
  • Histology is also not conclusive most of the time.

23
Clinical presentation
  • Symptoms of missed, anembryonic or incomplete
    abortion
  • Usually asymptomatic, but may present with
    hyperemesis gravidarum or pre-eclampsia

24
Human chorionic Gonadotropin
  • Secreted by active trophoblast of the placenta.
  • Detected in the blood 7-9 days after ovulation.
  • A concentration of 100mIU/ml is reached 2 days
    after the date of an expected menses.
  • Peak level of HCG ( app. 100,000mIU/ml ) - 10
    weeks of gestations
  • Declining and remaining at app 10,000-
    20,000mIU//ml by 12-14 weeks of gestation.

25
Rate of HCG rise
Below 1200 IU/L Doubles every 48-72hrs
From 1200 to 6000IU/L Doubles every 72-96 hrs
Above 6000IU/L Doubles every 4 days
26
Diagnostic Implications of Serum HCG levels
  • Single HCG value Not very informative
  • rate of increase in HCG levels varies as a
    pregnancy progresses.
  • Normal HCG values vary up to 20 times between
    different pregnancies,
  • An HCG that does not double every two to three
    days does not necessarily indicate a problem with
    the pregnancy.
  • Some normal pregnancies will have quite low
    levels of HCG, and result in perfect babies.

27
Challenges USG
  • As the vesicular degeneration is only partial,
    and delayed, USG findings are not clear as in
    complete mole.
  • Gestational sac is not measured routinely.
  • High resolution Transvaginal USG, and doppler
    flow study is not available widely.

28
Correlation between HCG level, and sonography
findings
  • Serum HCG levels 1800 IU/L-Gestational sac should
    be visible by USG
  • Serum HCG levels 5000IU/L-Cardiac pulsation
    should be visible.
  • More than 5000 IU/L rules out Ectopic pregnancy.

29
Serum HCG levels
From conception From Lmp IU/L
7days 3weeks 0to5
14days 28days 3to426
21days 35days 18 to 7,340
28days 42days 1080 to56,500
35-42days 49-56days 7,650 to 229,000
43-64days 57-78days 25,700 to 288,200
57-78days 79-100days 13,300 to 253,000
17-24weeks 2nd trimester 4060 to 65,400
After several days postpartum Non-pregnant levels

30
Diagnostic criteria by USG
  • Enlarged and cystic placenta with ill-defined
    fetal echoes, surrounded by a strongly refringent
    ring.
  • Transverse diameter is 1.5 times more than of AP
    diameter.

31
Ultrasonographic D/D
  • Hydropic degeneration of placenta
  • Complete mole with co-existent fetus
  • Leiomyoma of uterus
  • Retained products of conception
  • Choriocarcinoma
  • Missed Abortion
  • Blighted ovum
  • Ectopic pregnancy

32
Hydropic Degeneration of placenta
  • sonographic similarity of a hydropic placenta
    with marked swelling of the villi to molar
    tissue.
  • Vesicles, cysts, fetal remains, and an abnormal
    placenta can be seen.
  • The clinical history of the patient -diabetes,
    isoimmunization, and intragestational infection -
    should be considered
  • Beta HCG Generally lower

33
Hydatidiform Mole with co-existent foetus
  • Echogenic Intra-uterine tissue that is
    interspersed with numerous punctuated
    sonolucencies.
  • 8-12 weeks -Homogenously echogenic intraluminal
    tissue ( Max. Diam of villi 2mm) with separate
    normal placenta, and fetus.
  • 18-20 weeks Cystic spaces ( Max. diam. Of villi
    10mm). Molar tissue can cover normal placenta,
    thus difficult to differentiate from partial mole.

34
Uterine Leiomyoma
  • Areas of Hyaline degeneration can simulate the
    appearance of hemorrhage within mole.
  • Whorled internal consistency distinctly different
    than Vesicular pattern in mole.
  • Lack the cystic appearance of mole.

35
RPOC with Hemorrhage
  • Tissues of mixed echogenicity.
  • No gestational sac
  • Vesicular pattern will not be there.
  • Low levels of HCG.

36
Choriocarcinoma
  • No Villi
  • Well-circumscribed echogenic lesion in myometrium

37
Missed Abortions
  • Echo-refringent and non-homogeneous chorionic
    tissue remains either located inside the cavity
    or attached to the uterine wall.
  • Low or negative hCG levels.

38
Blighted ovum
  • The perfect interior delimitation of the
    embryonic sac.
  • No evidence of any embryo

39
Ectopic pregnancy
  • Pseudovesicles and a pseudosac
  • The combined use of quantitative determinations
    of hCG and vaginal ultrasound may resolve this
    uncertainty. 

40
Histopathology
  • Two populations of villi
  • Enlarged villi ( gt or 3-4mm) with central
    captivation
  • Irregular villi with geographic, scalloped border
    with trophoblastic inclusions
  • Trophoblast hyperplasia, usually focal.

41
Differential histopathology diagnosis
  • Beckwith-wiedeman syndrome
  • Twin gestation with complete mole, and
    co-existent fetus
  • Early complete hydatidiform mole
  • Hydropic spontaneous abortion
  • Placental Angiomatous malformation

42
Cytoflowmetry
  • Study of DNA content of curetted material.
  • Confirmation of Diagnosis specially when cofusion
    in diagnosis, or unnatural behaviour.
  • For Scientific reports
  • For research purpose.

43
Serum HCG levels after non trophoblastic Abortions
  • Should fall to undetectable level by 3 weeks.
  • Below 5mIUm/l - negative,
  • Above 25mIU/ml -positive.

44
HCG Levels after trophoblastic abortions
  • Greater than 500mIU/ml frequently by 3 weeks and
    usually by 6 weeks.
  • HCG titer should fall to a non-detectable level
    by 15 weeks.

45
HCG levels -Management
  • Indications of chemotherapy
  • Serum hCGgt 20, 000 IU/L at gt4 weeks.
  • Rising hCG. i.e. 2 consecutive rising serum
    samples.
  • hCG plateau. i.e. 3 consecutive serum samples not
    rising or falling significantly.
  • hCG still abnormal at 6 months post evacuation.

46
Conclusion
  • Partial Mole is a common, but under-diagnosed
    gestational trophoblastic disease.
  • combine use of serum HCG and ultrasonography in
    early pregnancy leads to suspicion of partial
    mole, and histology can confirm the diagnosis.
  • Early diagnosis, and use of prophylactic
    chemotherapy if indicated can prevent the
    development of chorio-carcinoma

47
Complete molar pregnancy,
48
USG-Normal Pregnancy
  • Double Decidual Sign
  • Intradecidual Sign

49
Blighted Ovum
  • The perfect interior delimitation of the
    embryonic sac.
  • No evidence of any embryo

50
Dr Haseena HamdaniAvicenna Medical
ClinicMedswana House, Machel Drive,
Gaboroneemail hhamdani_at_rediffmail.comPh No.
267- 3188808Cell 267- 71470419
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