Mrs. LPS, aged 31 years, married for 4 ½ years came to us on 11/7/2005 for primary infertility. She was a known case of poly cystic ovarian syndrome with menstrual cycles only on induction. Her ultrasound and diagnostic hysterolaparoscopy revealed a normal uterus with enlarged sclero cystic ovaries and bilateral patent tubes. The husband’s semen analysis was also normal.

The patient conceived in the first cycle of clomiphene citrate therapy with IUI. Her b-HCG level on the 32nd day was 3026.4mIU/ml (4/9/2006). The first transvaginal sonographic examination on the 40th day revealed triplet pregnancy. This underwent a natural reduction to twins at 7-8 weeks of gestation. During her routine antenatal scan with us at 11-12 weeks of gestation, there was a suspicion of a coexistent molar pregnancy with bilateral enlarged theca lutein cysts and she was referred to Mediscan (centre for sonology and fetal therapy) for a second opinion. They confirmed the presence of twin viable fetuses with molar pregnancy (Trichorionic Triamniotic triplets) in the third sac.

Due to a unfortunate previous experience with termination of ICSI twin pregnancy owing to complications, published in our newsletter earlier, we were anxious not to lose the otherwise normal appearing and viable twin pregnancy.

 
Her initial blood investigations were all normal and she did not have any history of hyperemesis or bleeding per vaginum as was with our previous case. At a follow up scan at 16 weeks it was noted that a separate cleavage plane existed between the placenta of fetus A and the mole and so it was confirmed to be a molar degeneration of the Fetus C. Thus we opted to continue the pregnancy until any expected complications arose. She then underwent stringent monitoring and regular antenatal check up.

At 30 weeks of gestation both fetuses were found to have asymmetric growth restriction with normal doppler study and a gradual increase in the volume of molar pregnancy as well. She was already on prophylactic therapy of antioxidants and amino acid infusion to combat it. She underwent an elective caesarean section on 19/03/2007 at 34 weeks of pregnancy owing to increasing volume of mole and fetal doppler changes, and delivered a boy and girl weighing 1.36kg and 1.24kg respectively. Intraoperatively there was no complication with regards to bleeding or evacuation of the molar products. Both mother and babies did well on discharge. The patient was followed up after delivery and her b-HCG values consistently reduced and was less than 1.0mIU/ml after 3 months of child birth.

In this case we did not have to perform any genetic testing of the coexisting viable fetuses as the mole was a separate entity by itself (trichorionic triamniotic). Literature review reports several cases of multiple gestation with molar pregnancies and varied outcomes. The dilemma with regards to termination may be overcome by careful analysis of the patient's physical condition, presence of known complications such as hyperemesis, thyrotoxicosis, hemorrhage and development of pregnancy induced hypertension. Serial ultrasound monitoring itself not only clinches diagnosis but also gives a volume of information on disease progression.
 
     
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