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By: PGI Kathleen Kaye A. Luceñara
Molar Pregnancy: “A sour and grapy encounter…”
IMPART
ARRIVEPRESENT
IDENTIFY DISCUSS
EXAMINE
Present a complete history and physical examination of the case
Arrive at a sound admitting impression and final diagnosis
Identify relevant differential diagnoses
Discuss the case comprehensively
Examine the management of the case
Impart updates and insights relevant to the case
General Information
• EV• 25 years old• Single• Filipino• Catholic• Office Worker• From Sto Tomas• Admitted: 1/21/15
Chief Complaint
Amenorrhea
7 w
ks P
TA
Amenorrhea Mild nausea and vomiting Vaginal spotting• Pregnancy Test - POSITIVE• No consult done at this time
4 d
ays
PTA
FIRST PRENATAL check up • USD done revealed:
ULTRASOUND RESULT
Cervix 2.7 x 2.4 cm Normal
Uterus 6.0 x 4.9 x 5 x 4cm
Normal size anteverted with no myometrial lesions
Endometrium 3.14 cmThickened and Hyperechoic with
multiple cystic spaces suggestive of molar gestation. No evidence of
gestational sac development
Right OvaryLeft Ovary
1.6 x 1.3 cm2.3 x 1.5 cm Normal in size and echotexture
Adnexae No lesions
Others (-) Free fluid in the cul-de-sac
Final Impression:Normal anteverted uterusThickened endometriumNormal ovariesT/C Molar Pregnancy
2 da
ys P
TA
Sought second opinion, USD was repeated with the following results:
ULTRASOUND RESULT
Cervix 3.41 x 2.53 x 2.33cm Normal
Uterus 7.27 x 6.13 x 5.48 Normal size anteverted
Right OvaryLeft Ovary
2.54 x 1.13 x 1.022.49 x 1.80 x 1.76
NormalNormal w/ corpus luteum
OthersWithin endometrial cavity are multiple cystic
structures of varying sizes. No fetus noted in this scan
Final Impression:Molar PregnancyNormal Ovaries BilateralWith corpus luteum, left ovary
ADMITTED• Scheduled for suction
curettage
OBSTETRIC HISTORYPRIMIGRAVID (G1P0)
LMP: Nov. 5, 2014 x 3-4 days x 2PPDPMP: Oct. 2, 2014 x 3-4 days x 2PPDEDC: Sept. 12, 2014AOG: 11 weeksMenarche: 14 years old Subsequently: 28-30-day cycles x 3-4 days
x 2 PPD; (+) Dysmenorrhea
No known allergies to food or drugs
Non – Diabetic Non-Asthmatic Non-Hypertensive
PAST MEDICAL HISTORY
PERSONAL-SOCIAL HISTORY
Office worker
Smoker
Alcoholic-beverage drinkerc
FAMILY HISTORY
Unremarkable
REVIEW OF SYSTEMS
GENERAL SKIN EENT RESPIR CARDIO
Weight Loss Rashes Dysphagia Cough
Colds
Palpitations
URINARY GYNECOLOGIC MUSCULO- HEMA- GASTRO
Dysuria
Hematuria
Discharges Joint Pains Bleeding Gums
Epistaxis
Abdominal Pain
Changes in BM
Unremarkable
PHYSICAL EXAMINATION
General
Awake Conscious and responsive Not in respiratory distress
Vital SignsT :36.9°CRR :19 cpm CR :79 bpmBP :120/70 mmHgWeight :56.5 KgHeight : 5’4”BMI : 21.26 (Normal)
Skin
I: • No pallor • No mottling• No discolorations or rashes
P: Good skin turgor, warm to touch
Head
I: • Round with smooth skull
contour
P: No nodules noted
Eye
I: • Anicteric Sclera• Pink palpebral conjunctiva
Ears
I: • Symmetrical, aligned with the
outer canthus of the eye
P: Elastic with good recoil
Nose
I: • Symmetrical and straight• No nasal flaring noted• Nasal septum is in midline
Mouth and Throat
I: • Lips are pink and moist• Oral mucosa is moist• Tongue moist and in midline • Tonsillopharyngeal area is not
hyperemic with no exudates
Neck
I: • Neck is midline• Non-distended veins• No anterior neck masses
P: Lymph nodes are not palpable and not tender
ChestI: With symmetrical chest expansion and no retractions noted
P: Lung fields are resonant upon percussion
P: With symmetrical chest expansion
A: No crackles on both mid-lower lung fields
Cardiovascular
I: With adynamic precordium
A:• Regular cardiac rate and rhythm• PMI at 5th ICS 7cm from the
midsternum• No murmurs• With full pulsation of peripheral
pulses
Abdomen
• Flabby• Soft and undistended• No tenderness • Uterus palpated at the level of
the symphysis pubis
Internal Examination
I: inserts two fingers with ease
C: soft but closed
U: slightly enlarged
A: not enlarged, no tenderness
D: no discharge
Extremities
I: • Grossly normal muscle size and tone • No gross deformities or contractures
P: • CRT < 3s • Pulses are strong and not easily
obliterated by pressure
Neuro
General• No cranial nerve deficits• No sensory or motor deficits
125
SALIENT FEATURES (HISTORY)
2Primigravid
3Amenorrhea for 11 weeks
4
5USD: Endometrium is hyperechoic,
thickened w/ cystic spaces
6USD: No gestational sac
7No vaginal Spotting
9Unremarkable Family Hx
5 10
Unremarkable ROS
Minimal Nausea & Vomiting
Positive PT
1Uterus palpable at the level of
the symphisis pubis
SALIENT FEATURES (PE)
2IE: slightly enlarged uterus
3IE: no tenderness
4
5
IE: unremarkable adnexae
IE: no discharge
IMPRESSION
Hydatidiform Mole, G1P0
DIFFERENTIALS
Amenorrhea and (+) PT
Pregnancy Gestational Trophoblastic DiseasePregnancy
DIFFERENTIALS
Pregnancy
Ectopic Pregnancy
Normal Pregnancy
ECTOPIC PREGNANCYImplantation of the blastocyst anywhere outside the uterus, 96% of the time in the
FALLOPIAN TUBE
RULE-IN RULE- OUT Amenorrhea for 11 weeks No abdominal pain or tenderness
Positive pregnancy test No vaginal bleeding or spotting
Absence of gestational sac the uterus
No adnexal abnormalities via USD
Mild nausea and vomiting No adnexal or cervical motion tenderness noted on IE
DIFFERENTIALS
Pregnancy
Ectopic Pregnancy
Normal Pregnancy
NORMAL PREGNANCYRULE-IN RULE- OUT
Amenorrhea for 11 weeks No gestational sac or fetus noted
via USD Positive pregnancy test
Mild nausea and vomiting
DIFFERENTIALS
Amenorrhea and (+) PT
Pregnancy MolarGestational Trophoblastic Disease
Gestational Trophoblastic Disease
Gestational Trophoblastic Disease
RULE-IN RULE- OUT Amenorrhea for 11 weeks
Cannot be ruled out
Positive pregnancy test
Absence of gestational sac the uterus with thickened and hyerechoic endometrium with cystic spaces.
Mild nausea and vomiting
Abnormal trophoblast proliferation: hydatidiform moles and non-molar
trophoblastic neoplasms
DAY
0 Admitted to ROOM OF CHOICE Placed on diet as tolerated then
placed on Nothing per orem after midnight
Vital signs monitored Scheduled for suction curettage Evening Primrose 2 soft gels
inserted per vagina every 6 hours Misoprostol one tab inserted per
vagina 3 hours prior to OR
DAY
0 LABS:
• Complete Blood Count• Blood typing• Pregnancy Test•Beta HcG (Quanitative)
COMPLETE BLOOD COUNTHemoglobin 124
RBC 4.13
Leukocytes 9.9
Neutrophil 0.81
Lymphocytes 0.15
Monocyte 0.04
Hematocrit 0.40
Thrombocytes 314
BLOOD TYPE O +
Pregnancy TestPositive
Serum HcG (Quanti)>1,500 mIU/mL
(Normal: 75,300mIU/mL)
DAY
1 OPERATIVE TECHNIQUE:1. Induction via spinal anesthesia2. Placed on dorsal lithotomy 3. Asepsis/antisepsis was done4. Sterile Drapes applied at lower
extremities5. Bladder was emptied6. Pelvic Examination was done7. Sims vaginal retractor was
applied at posterior vaginal wall
DAY
1 OPERATIVE TECHNIQUE:8. Anterior lip of cervix was grasped
with tenaculum9. Suction cannula was introduced
through the cervix all the way to the fundus
10. Approx. 100cc of vesicular tissues admixed with blood were suctioned
11. Sharp curette was applied after suctioning
DAY
1 OPERATIVE TECHNIQUE:
12. Perineal Washing done13. Specimen was sent for histopath14. End of procedure
OPERATIVE FINDINGS
Cervix is pink and smooth. Uterus was slightly enlarged. Vesicular Tissues admixed
with blood approximately 100 mL were suctioned
Day 1 (Immediately Post-Op)KEY EVENTS PROBLEM MANAGEMENT
(+) minimal vaginal bleeding
No complains of pain
Stable Vital Signs
Molar Pregnancy, G1P0, S/P Suction
and Sharp Curettage
Monitored at the PACU
Meds:1. Cefalexin
500mg/tab three times daily
2.Methergin 1 tab every 4 hours x 6 doses
3.Mefenamic acid 500mg every 6 hours x 1 day
T :36.0 to 36.4RR :19 to 20PR :80s to 90sBP :100-110/60-80
Day 2 (1st Post-Op Day)KEY EVENTS PROBLEM MANAGEMENT
(+) minimal vaginal bleeding
No complains of pain
Stable Vital Signs Repeat Serum Beta
HcG
Molar Pregnancy, G1P0, S/P Suction
and Sharp Curettage
Cleared for discharge with Take-home
Meds:1. Cefalexin
500mg/tab three times daily x 6 days
2. Methergin 1 tab TID x 3 days
3.MVT 1 cap OD x 1 monthT :36.0 to 36.4
RR :19 to 20PR :80s to 90sBP :100-110/60-80
Serum HcG (Quanti)106,155 mIU/mL
FINAL DIAGNOSIS
Hydatidiform Mole, G1P0 (0010)
Hydatidiform MoleExcessively edematous immature
placentas, which include the following:
1. Complete H. Mole2. Partial H. Mole3. Invasive Mole
MALIGNANT: marked penetration, destruction
of myometrium and ability to metastasize
Epidemiology and Risk Factors
• 13 in every 1000 pregnancy • Ethnicity: Asians, Hispanics and American
Indiants• Age: adolescents and women (36 – 40y.o.) women (older than 40) • History of a previous mole: previous complete mole – 1.5% risk previous partial mole – 2.7 % two molar pregnancies – 23%
Pathology
Partial vs Complete
Beta-HcG
• Hormone produced by the syncytiotrophoblast of the placenta
• Homologues: LH, TSH and FSH• Doubling Time: 48 - 72 hours• Half life: 24 – 36 hours normal
after 5 to 7 days• Associated with morning sickness
Beta-HcG
• First detected: 11 days after conception and about 12 – 14 days after conception by a urine test
• Peak: 8 to 11 weeks of pregnancy
• Nadir: 16 weeks of pregnancy
Clinical Manifestations• Amenorrhea• Irregular bleeding• Uterus large for gestational age• Significant nausea and vomiting • Theca lutein cysts, Elevated FT4 and
decreased TSH• Severe pre-eclampsia and eclampsia
Clinical ManifestationsIn the advent of sonography, majority of molar
pregnancies today are recognized EARLY
• Diagnosis after 1 to 2 months of amenorrhea• Diagnosed at a mean AOG of 10 weeks• 41% of women with molar pregnancy are
asymptomatic
DIAGNOSISSonographyMainstay of diagnosisCOMPLETE MOLE:Echogenic uterine mass
with anechoic cystic spaces without a fetus or amniotic sac
“SNOWSTORM” appearance
DIAGNOSISSonography
PARTIAL MOLE:Thickened multicystic
placenta with fetus
The overall sensitivity and positive predictive value for the ultrasound diagnosis of hydatidiform mole was 44% and 48% (Kirk et al., 2007)
DIAGNOSISSerum HcG
commonly elevated above expected for
gestational age
MANAGEMENT• Screen for complications• Termination of molar pregnancy• Recommended: Suction curettage• Preoperative cervical dilatation with an osmotic
agent is recommended if the cervix is minimally dilated
Post-evacuation Surveillance
POST-EVACUATION SURVEILLANCE
Reliable contraceptionReview pathology reportSerial serum beta HcG measurements
UNDETECTABLE: 7 weeks (partial); 9 weeks (Complete)
Plateauing or Increasing levels: suspect GTN 15 – 20% risk for complete moles1% – 5% risk for partial moles
UPDATE
GOAL: To systematically review the evidence for the effectiveness and safety of P-Chem to prevent GTN in women with a molar pregnancy.
OUTCOME: The time to diagnosis was longer in the P-Chem group than the control group (2 studies, 33 participants; mean difference (MD) 28.72; 95% CI 13.19 to 44.24; P = 0.0003) and the P-Chem group required more courses to cure subsequent GTN (1 poor-quality study, 14 participants; MD 1.10; 95% CI 0.52 to 1.68; P = 0.0002).
Fu et al. (2012)
UPDATE
CONCLUSION: P-Chem may reduce the risk of progression to GTN in women with CMs who are at a high risk of malignant transformation; however, current evidence in favour of P-Chem is limited by the poor methodological quality and small size of the included studies. As P-Chem may increase drug resistance, delay treatment of GTN and expose women unnecessarily to toxic side effects, this practice cannot currently be recommended.
Kumar et al. (2015)
Thank you!