OB Case Presentation
Download
Report
Transcript OB Case Presentation
OB CASE PRESENTATION
Tan, Irene Carmelle S.
GENERAL DATA
M.A. is a 32 year old, G3P2 (2012), married,
Filipino, Catholic, currently residing in Antipolo
was admitted in QMMC
Chief complaint
vaginal bleeding
HISTORY OF PRESENT PREGNANCY
LMP: January 9,2011
EDC: October 16, 2011
AOG: 14 2/7 weeks AOG by UTZ
HISTORY OF PRESENT PREGNANCY
2months PTC
the patient did not have her menstrual period
No pregnancy test was done.
1 month PTC
having hypogastric pain which was described as
squeezing and rated as 7/10 severity
pain lasted for 10-30mins
took Mefenamic acid once
pain was accompanied by vaginal bleeding which
was described as red droplet
She went to the center and consulted.
Pregnancy test was done and the result was
positive.
No intervention was done.
Few weeks PTC
hypogastric pain and bleeding persisted and the
volume of blood expelled was greater than before
She now consulted a lying in and ultrasound was
done.
Result showed that the patient has hydatidiform
mole which prompted the patient to be admitted
in QMMC.
Obstetric history
G 3P2 (2012)
Year
birth
of Place
Method of Complicat
delivery ion
1st
2006
pregnancy
QMMC
NSD
None
2nd
2007
pregnancy
House
NSD
None
3rd
2011
pregnancy
QMMC
Suction
none
and
curettage
PAST MEDICAL HISTORY
denied of having Diabetes Mellitus, hypertension,
asthma, pulmonary tuberculosis, allergies, renal
diseases, goiter, cancer and other illness
patient did not undergo any surgeries
no history of blood transfusion, accidents or
childhood illness
FAMILY HISTORY
Father: (-) hypertension, diabetes mellitus,
cardiovascular disease, asthma, stroke
Mother: (+) hypertension, (-) diabetes mellitus,
cardiovascular disease, asthma, stroke
PERSONAL AND SOCIAL HISTORY
Works as a masseuse
Non-smoker and an occasional alcoholic
beverage drinker
No illicit drug use
Her husband is a cigarette vendor
They have been together for 3 years.
SEXUAL HISTORY
First sexual intercourse →18 y/o.
The patient and her current partner are
monogamous.
She has no history of sexually transmitted
diseases.
Unremrkable ROS and PE
CONTRACEPTIVE HISTORY
used intrauterine device from 2008-2010
stopped using intrauterine device because she
wanted to get pregnant again
DIAGNOSIS
Admitting diagnosis
G3P2 (2002) Molar pregnancy 14 2/7 weeks AOG
by UTZ
Post-op diagnosis
G3P2 (2012) Molar pregnancy 14 2/7 weeks AOG
by UTZ
COURSE IN THE WARD
Medications given:
Ampicillin 1g TIV every 6 hrs
Hyoscine N-Butyl Bromide 1 amp every 4 hrs
Ranitidine 50mg IV
Cefalexin 500mg every 8hrs x 7 days
Methergin 1 tab 3x/day for 3 days
Oxytocin 10%
Ascorbic acid 1 tab once a day
Ferrous sulfate 1 tab once a day
Mefenamic acid 500mg 1 tab per needed
Blood chemistry
Urinalysis
RBC
2.94 x10 /L
↓
Color
Yellow
Hemoglobin
84 g/L
↓
Transparency
Slightly hazy
Hematocrit
0.26 %
↓
Reaction
6.5
MCV
87.1/ L
Specific gravity
1.020
MCH
28.6 pg
WBC
0-1
MCHC
32.9 %
RBC
15-20
Platelet
adequate
Epithelial cells
few
WBC
25.6 x10 /L
↑
Bacteria
Few
Neutrophil
0.837
↑
Mucus threads
moderate
Albumin
Negative
Prothrombin time
10.8 sec
Sugar
Negative
PT INR
0.90
Ketones
Negative
APTT
39.2 sec
BUN
2.71 mmol/L
Creatinine
57.87 umol/L
AST
22 U/L
ALT
32 U/L
Sodium
133
Potassium
3.5
Chloride
101
TSH
0.026
FT4
16.55
B HCG
361,601
↓
↑
↓
↓
↑
The patient was tranfused one unit of packed
RBC
HYDATIDIFORM MOLE
Characterized by presence of avascular cystic villi
89.6 % of all trophoblastic disease
TYPES :
Partial Mole : presence of some normal villi with
anucleated RBCs
Complete Mole : complete absence of normal villi
has three morphologic characteristics:
(1) a mass of vesicles (distended villi) that appear
as large, grapelike dilations
(2) a loss of fetal blood vessels, which are either
diminished or absent from the villi
(3) hyperplasia of the syncytiotrophoblast and
cytotrophoblast
EPIDEMIOLOGY
United States→the rate is estimated to be
approximately one in 1500 to 2000 pregnancies
and in one in 600 therapeutic abortions
(Berkowitz and associates and Eifel and
associates )
rates from Southeast Asia are 5 to 15 times
higher with much larger variations, and rates up
to 13 per 1000 have been reported by Altieri and
colleagues.
RISK FACTORS
Risk increases with age, greatest risk >40 y/o
Increase risk in <20 y/o
History of hydatidiform mole →increases risk 2040x
Previous recurrent spontaneous abortion
Lower socioeconomic status as well as in
underdeveloped areas → poor nutrition
Mexicans and Filipinos appear to have elevated
rates compared with Japanese and Chinese.
feature
Complete mole
Incomplete mole
Fetal or embryonic
tissue
Absent
Present
Hydatidiform
Diffuse
swelling of embryonic
villi
Focal
Trophoblastic
hyperplasia
Diffuse
Focal
Trophoblastic
stromal inclusions
Absent
Present
Genetic percentage
Paternal
Bipaternal
Karyotype
46XX; 46XY
69XXY; 69XYY
Persistent human
chorionic
gonadotropin
20% of cases
0.5% of cases
COMPLETE MOLE
No fetus or normal
villi present
Trophoblastic
proliferation
Marked villous
hydrops
Absence of blood
vessels in villi
Bunch of grapes
appearance
PARTIAL MOLE
Fetus and some
normal villi are
present
Focal villous hydrops
Blood vessels and
RBCs present
Gross fetal parts
present
COMPLETE MOLE
Clinical Presentation : 1st or early 2nd trimester
Large for date uterus (50 % of cases)
Contents expelled earlier (~10-16 weeks)
Early onset of Preeclampsia
β-HCG titer is higher than partial mole
UTZ : no fetal parts
↑ risk of Choriocarcinoma
PARTIAL MOLE
Clinical Presentation : 2nd trimester
Normal or Small for date uterus
Contents are expelled later (~10-26 weeks)
Normal symptoms of pregnancy
β-HCG titer is lower than complete mole
UTZ : (+) fetal components
Lower risk of Choriocarcinoma
SIGNS AND SYMPTOMS
Vaginal bleeding
Hypogastric pain
Amenorrhea
Enlargement of Abdomen
Others:
86
14.2
8.5
3.9
%
No FHT by Doppler after 12 weeks
Hyperemesis gravidarum
Sxs of preeclampsia
Sxs of hyperthyroidism
Lung , liver , brain involvement
DIAGNOSIS
Clinical Symptoms
UTZ : “ snow-storm appearance”/ honeycomb
pattern
β - HCG titers :
>100,000 IU/l on 100th day from LMP
* Normal Pregnancy HCG goes down
on the 60th-70th day from LMP
UTZ : SNOWSTORM OR HONEYCOMB
PATTERN
Metastasis
Common sites: lungs, liver, brain
Other tests to request:
CXR : Rule out lung metastasis; “canon-ball”
exudates
SGPT/SGOT : rule out liver metastasis
Baseline liver function prior
to chemotherapy
BUN/Creatinine : Baseline kidney function prior
to chemotherapy
CBC
FIGO-WHO scoring system (2002)
score
0
1
2
4
Age
<39
>39
--
--
Antecedent
pregnancy
H. Mole
Abortion
Term
--
Months from
index
pregnancy
<4 mos
4-6
7-12
>12
Pretreatment
HCG
<1000
1000-10,000
10,000-100,000
>100,000
Largest tumor
size
<3cm
3-5cm
>5cm
--
Site of
metastasis
--
Spleen, kidney
GI
Brain, liver
Number of
metastasis
0
1-4
5-6
>8
Previous
chemotherapy
--
--
Single agent
2 or more
drugs
TREATMENT
Termination of Molar Pregnancy
Evacuation by Suction Curettage
IV oxytocin given
Low incidence of uterine perforation
and embolization
Fertility is preserved
Replacement of blood loss
Treatment of infection
Prophylactic chemotherapy
Can be given before or after
evacuation or hysterectomy
*Methotrexate
*Actinomycin
Low risk→score of 0-6
methotrexate combined w/ folinic acid
High risk → score of >7
combination of
etoposide/methotrexate/dactinomycin and
cyclophosphamide/vincristine
INDICATIONS FOR INITIATING CHEMOTHERAPY
FOLLOWING MOLAR PREGNANCY
Brain, liver, GI or lung mets >2cm on chest X-ray
Histological evidence of choriocarcinoma
Heavy vaginal bleeding or GI intraperitoneal
bleeding
Pulmonary, vulvar or vaginal metastases unless
the HCG level is falling
Rising HCG in 2 consecutive serum samples
HCG > 20,000 iu/l > 4weeks after evacuation
HCG plateau in 3 consecutive serum samples
Raised HCG level 6 months after evacuation
FOLLOW UP
β-HCG titers q weekly until negative (less than 5
mIu/ml) for 3 consecutive determinations then q
1-3 months until 1 year
CXR q 3 months x 1 year
* for early detection of lung mets
Prevent pregnancy for 1 year
* combination OCPs
METHOTREXATE
Pulse MTX : 40 mg/m² IM weekly
MTX with Folinic Acid Rescue
Day 1 , 3 , 5 , 7 :
MTX 1.0 mg/kg/day IM or IV
Day 2 , 4 , 6 , 8 :
Folinic Acid 0.1 mg/kg/day
ACTINOMYCIN D
5 Day Actinomycin D :
12 μg/kg IV daily x 5 days
CBC,platelet count,SGOT daily
(+) response : retreat at the same dose
(-) response : add 2 μg/kg to the initial
dose or switch to MTX
Pulse Actinomycin D : 1.25 mg/m² q 2 weeks
PROGNOSIS
Good Prognosis
duration < 4 months
pre-evacuation β-HCG titers < 100,000 Iu/L
β-HCG undetectable in 4 weeks
Histologic type :
Partial mole is better than Complete mole
Risk of developing a 2nd molar pregnancy is 1 – 3
%
Thank you