- Case report
- Open Access
When a vesicular placenta meets a live fetus: case report of twin pregnancy with a partial hydatidiform mole
BMC Pregnancy and Childbirth volume 21, Article number: 694 (2021)
Hydatidiform moles exhibit a distinctive gross appearance of multiple vesicles in the placenta. The advances in cytogenetic technologies have helped uncover novel entities of hydatidiform moles and enabled elaborate diagnoses. However, management of a vesicular placenta with a coexistent live fetus poses a bigger challenge beyond hydatidiform moles.
A 33-year-old woman was referred to our department for suspected hydatidiform mole coexistent with a live fetus at 24 weeks’ gestation. The patient had conceived through double embryo transplantation, and first-trimester ultrasonography displayed a single sac. Mid-trimester imaging findings of normal placenta parenchyma admixed with multiple vesicles and a single amniotic cavity with a fetus led to suspicion of a singleton partial molar pregnancy. After confirmation of a normal diploid by amniocentesis and close surveillance, the patient delivered a healthy neonate. Preliminary microscopic examination of the placenta failed to clarify the diagnosis until fluorescence in situ hybridization showed a majority of XXY sex chromosomes. The patient developed suspected choriocarcinoma and achieved remission for 5 months after chemotherapy, but relapsed with suspected intermediate trophoblastic tumor.
We report a rare case of twin pregnancy comprising a partial mole and a normal fetus that resembled a singleton partial molar pregnancy. Individualized care is important in conditions where a vesicular placenta coexists with a fetus. We strongly recommend ancillary examinations in addition to traditional morphologic assessment in such cases.
Due to the distinctive gross appearance, hydatidiform moles (molar pregnancies) have been described since the fourth century BC . The incidence of hydatidiform moles varies in different ethnic groups, with an estimated incidence of 2.43–13 per 1000 pregnancies in Asians and 0.5–1.84 in Caucasians [2, 3]. Since the late 1970s, hydatidiform moles have been classified as complete and partial hydatidiform moles based on the genetic and histopathologic features . Classically, complete moles are androgenetic diploid, and partial moles are diandric monogynic triploid. The ratio of partial to complete moles is approximately 1.5–1.8 [5, 6]. In recent years, familial biparental complete moles, mosaic complete moles, and tetraploid partial moles have been reported . In 1991, placental mesenchymal dysplasia (PMD) was proposed as a novel pathological entity resembling hydatidiform moles . The estimated incidence of PMD was reported to be two per 10,000 pregnancies, but this is probably an underestimate . Features of PMD are analogous to those of partial moles and may include cystic placenta, elevated human chorionic gonadotropin (HCG) levels, fetal abnormalities, and preeclampsia .
Coexistence of a vesicular placenta with a fetus is a rarer phenomenon which encompasses four categories: dizygotic twin pregnancy involving a fetus and a coexistent complete or partial mole; singleton pregnancy of a partial mole with a malformed triploid fetus; a mosaic complete or partial mole with a mosaic fetus, or a mosaic mole with an euploid fetus (confined placental mosaicism, CPM); and PMD [10,11,12,13,14,15,16,17]. Intriguingly, the reported incidence of twin pregnancy with a complete mole is one per 10,000–100,000 pregnancies [18, 19], whilst twin pregnancies with a partial mole are even rare , which is possibly due to the high first-trimester miscarriage rate for partial moles . A mosaic complete or partial mole with a fetus is the rarest entity, as reported in a few articles [12,13,14,15,16]. Apart from a possibly malformed fetus, the other potential complications of hydatidiform mole coexisting with a fetus include vaginal bleeding, hyperthyroidism, preeclampsia, fetal death, fetal growth restriction (FGR), preterm birth, hyperemesis, fetal-maternal hemorrhage, and gestational trophoblastic neoplasia (GTN) [13, 14, 21]. The above four categories of coexisting vesicular placenta with fetus have similar presentations but different prognosis. Therefore, prenatal diagnosis and management in these cases is not straightforward owing to the possibility of a healthy fetus.
We report a case of suspected singleton partial mole with a structurally and karyotypically normal fetus. Postnatal placental morphological examination failed to provide a precise diagnosis in the first place. Thus, we investigated the case and performed a literature review of the diagnosis and management of vesicular placenta with a fetus.
A 33-year-old woman, gravida 2 para 0, was referred to our fetal medicine department for a suspected hydatidiform mole coexistent with a live fetus at 24 weeks’ gestation. Her first pregnancy was a miscarriage around 5 weeks’ gestation conceived by in vitro fertilization (IVF) a year ago. She had no family history of twin pregnancy or hydatidiform mole. She had conceived through transfer of 2 day-5 embryos following IVF although the indication for double rather than single embryo transfer was obscure.
Several ultrasound examinations performed during the first trimester displayed a single sac containing a fetus with no signs of placental abnormalities. Her thyroid hormone levels were normal, but her first trimester hCG and prenatal genetic screening results were not available. At the time of her visit, the gestational age was 24 weeks. She had no vaginal spotting and her blood pressure was normal. Her serum β-human chorionic gonadotropin (β-hCG) level was 105,851 IU/L. Ultrasound evaluation revealed a structurally normal fetus with an intraplacental multicystic mass measuring 154 mm × 53 mm; no theca lutein cysts were observed. Magnetic resonance imaging (MRI) showed a placenta with a normally-appearing portion abutted by multicystic mass with high signal on T2-weighted images at the right anterior wall (Fig. 1). The 151 mm × 139 mm × 67 mm multicystic mass was partly admixed with the normal placenta and partly bulged between the normal placenta and the amniotic sac. There were no signs of aneurismal or varicose dilation of fetal chorionic vessels. Her chest X-ray was normal.
Amniocentesis revealed a 46, XX karyotype without pathological copy number variants. At this point the working diagnosis was twin pregnancy with a partial mole or CPM with a partial mole, coexisting with a normal fetus. The patient was counselled regarding the potential maternal and fetal risks associated with pregnancies with hydatidiform moles, following which the patient decided to continue the pregnancy. She was monitored closely. Serial ultrasonographic evaluation of the conceptus performed once every 2 or 3 weeks showed a normally-growing fetus and a persistent and slightly-diminishing multicystic mass measuring 110 mm × 106 mm × 24 mm at 37 weeks’ gestation.
She remained asymptomatic with normal blood pressure. Her serum β-hCG levels peaked around 105,000 IU/L at 25–26 weeks’ gestation and gradually declined to 17,483 IU/L at delivery (Fig. 2). At 402/7 weeks’ gestation, ultrasound examination showed a fetus with an estimated weight of 2745 g (5.4th percentile for the gestational age according to the NICHD fetal growth curve for Asians ) and a deepest vertical amniotic fluid pocket of 11 mm. Considering the oligohydramnios and the risk of potential metastasis of trophoblastic cells by uterine contractions during vaginal delivery, cesarean section was performed and a female neonate was delivered without any complications. The Apgar scores at 1 and 5 min were 9 and 10, respectively. The neonate weighed 2840 g (8th percentile for gestational age) and had no gross anomalies. Macroscopic examination of the placenta showed an adjacent mass (10 cm × 7 cm × 1 cm) of multiple cysts of varying sizes (Fig. 3). The mass was partly intermediate between the normal-looking placental parenchyma and chorionic membranes. Thin parenchyma was also noted on the area of chorionic plate near the mass.
Histopathological examination of the normal part of the main placenta revealed features of a normal mature placenta. The cystic mass showed large, hydropic villi, circumferential trophoblastic hyperplasia (Fig. 4a), which was partly necrotic. Histopathological classification (complete or partial mole) was inconclusive. DNA was extracted from a few rinsed macroscopic vesicles, and samples of normal placenta, amniotic fluid, and parental peripheral blood. Twenty short tandem repeat (STR) loci were tested using AmpFlSTR-Identifiler-PCR kit according to the manufacturer’s instructions (Thermo Fisher Scientific). The amniotic fluid and normal placenta DNA showed the same balanced biallelic profiles of both paternal and maternal contributions, with no additional suspicious peaks. However, the vesicular tissue exhibited predominantly all maternal alleles at all loci with pretty small peaks of homozygous or heterozygous paternal alleles at a few loci, which was probably attributable to the contamination of maternal decidua and necrosis of molar tissue.
To rule out familial recurrent complete mole owing to the patient’s history of an early miscarriage and a molar pregnancy, Sanger sequencing of NLRP7 (19q13.42) and KHDC3L (6q13) were performed on genomic DNA extracted from the patient’s blood, which showed no mutations. Immunohistochemical staining for p57KIP2 expression in the molar tissue showed focal positivity in the villi (Fig. 4b). Finally, fluorescence in situ hybridization (FISH) for the X and Y chromosomes on the slide of molar tissue was performed. Two hundred cells were scored and XXY was observed in 88% of cells (Fig. 4c). The rest were XXXYY (7%) and XYY (5%), which was considered interference by syncytiotrophoblast and loss of nuclear components due to slicing. Until this point, a partial mole was ascertained despite lack of genetic test results and we favored the diagnosis of a twin pregnancy over CPM due to the relatively clear margin of the molar lesion from the normal placenta and normal chromosomes of the fetus.
The patient’s serum β-hCG was maintained around 100 IU/L 3 months postpartum; thus, she was diagnosed with GTN and underwent four courses of single-agent chemotherapy using dactinomycin. However, she did not follow medical advice to receive the subsequent courses. One year later, chest computed tomography showed several lung nodules suggestive of pulmonary metastases. Core needle biopsy of lung nodules revealed a large area of coagulative necrosis and a small cluster of tumor cells with marked atypia. Immunostaining for CK and beta-hCG were positive and 50% of tumor cells stained positive for p53. The initial diagnosis was reported as metastatic trophoblastic tumor. However, due to the small amount of tumor cells, we were not able to further classify or perform genotyping of lung biopsy.
The patient was diagnosed as choriocarcinoma and received multiagent regimens of EMA/CO (etoposide, methotrexate, actinomycin D, cyclophosphamide and vincristine [oncovin]). Her β-hCG levels returned to normal after six treatment cycles. She received another three cycles and was in remission for 5 months; however, she relapsed showing mild elevation of β-hCG level and increase in lung nodules but no uterine mass was observed. The attending gynecologist suspected intermediate trophoblastic tumor due to the relatively low levels of β-hCG and her insensitivity to chemotherapy. She was scheduled to undergo partial pulmonary lobectomy. Her child is developing normally at 29 months.
Discussion and conclusions
We report a rare case of twin pregnancy with a partial mole and a coexisting normal fetus. Comprehensive evaluation and close monitoring of the pregnancy led to delivery of a healthy baby. The biggest challenge of this case was the diagnosis. During the gestational period, we were uncertain whether it was a twin pregnancy consisting of a hydatidiform mole and a fetus or a singleton pregnancy of CPM associated with a mole. Prenatal imaging showed intermixing of the multicystic mass with the normal placenta, leading to suspicion of a singleton partial mole. On macroscopic examination of specimen, the mass exhibited a morphology that was partly intermediate between the normal placental parenchyma and chorionic membranes, which was consistent with the prenatal images. However, on gross examination, the molar mass was found to have abutted into the normal placenta (rather than intermixed) and there was a clear boundary between the two elements. In a recent review the percentage of mosaicism in CPM placenta biopsies was 32.5–100% (IQR), with a median of 100% . Thus, the fact that STR of normal placenta DNA showed balanced biparental profiles favored the diagnosis of a twin pregnancy rather than CPM . Early ultrasonography showed a single sac probably because a subtle molar mass is hard to discern by ultrasound if it accompanies a well-developed placenta . Prenatal images with an intermixing pattern could be explained by reduction of tumor size in prenatal imaging and corresponding decrease in serum β-hCG. A focal area of thin chorionic plate in the normal placenta adjacent to the mass possibly represented recession of the mole. Previous reports of twin pregnancies with a hydatidiform mole stated a clear boundary between normal placenta and molar tissue . Such a growing pattern of a hydatidiform mole into another normal placenta has not been described before.
Based on a review of literature, we summarized all conditions wherein a vesicular placenta may coexist with a fetus. These include: (1) dizygotic twin pregnancy with a fetus and a coexistent complete or partial mole; (2) singleton pregnancy of a partial mole with a malformed triploid fetus; (3) a mosaic complete or partial mole with a mosaic fetus, or a mosaic mole with an euploid fetus (CPM); (4) PMD [10,11,12,13,14,15,16,17]. Genetically, karyotypes of complete moles are 46, XX (90%) or 46, XY (10%) ; karyotypes of partial moles are 69, XXY, 69, XXX, or 69, XYY (70, 27, 3%) . A mosaic complete or partial mole with a mosaic fetus, or a mosaic mole with a euploid fetus (CPM) is the rarest type which can be confirmed by molecular genotyping [14,15,16]. PMD is sometimes associated with Beckwith-Wiedemann syndrome (BWS) and androgenetic/biparental mosaicism .
In literature review, we identified a few common misconceptions about hydatidiform moles. First, diploid partial moles probably do not exist due to the lack of underlying genetic pathogenesis, but were reported in some case reports [3, 15]. Second, evidence of a fetus in a partial mole could be either an amniotic sac containing a fetus or nucleated red blood cells in villous capillaries - the latter phenomenon is less known [28, 29]. Last but not least, although histologic differentiation of hydropic villi has been described numerously, quite a few studies have demonstrated significant interobserver and intra-observer variability in the diagnosis of hydatidiform moles, hydropic abortion, and PMD based solely on traditional hematoxylin-eosin-stained morphologic assessment, even by specialized pathological experts [30,31,32,33]. For example, Malgorzata G et al. reported termination of an initially-diagnosed twin pregnancy with a complete mole and a coexistent fetus based on histopathological assessment; however, they made a final diagnosis of twin with a partial mole by p57KIP2 immunostaining reassessment . Therefore, pathological diagnosis may not be the gold standard in molar cases .
Researchers have advocated selective use of ancillary techniques such as p57KIP2 immunostaining, FISH, STR genotyping (microsatellite genotyping) or SNP-based microarray analysis to refine the diagnosis [6, 30, 35, 36]. P57KIP2 is a protein encoded by the imprinted maternally expressed gene CDKN1C located on chromosome 11p15.5; thus p57KIP2 immunostaining is negative in androgenetic complete moles and diandric triploid partial moles with loss of maternal chromosome 11 , while it is positive in different groups of certain cells under other circumstances (biparental complete moles, mosaic complete moles, complete moles with a retaining maternal chromosome 11 , partial moles, PMD, non-molar products of conception) . Focally-positive p57KIP2 immunostaining observed in our case can be interpreted as positive, as has been clarified in previous studies . FISH with a set of chromosome enumeration probes (CEP) for chromosomes X, Y and other autosomes is another efficient means for arriving at a definitive diagnosis, or literally a critical one as demonstrated in our case.
Molecular genotyping determines the parental source and ratios of polymorphic alleles by comparing villous and parental DNA patterns and is suggested as an ultimate method for diagnosis . In the present case, STR results of molar tissue displayed predominantly two maternal alleles, which we reckon was attributable to contamination by maternal decidua and necrosis of tumor cells. Such contamination has been reported in previous placenta research studies and is sometimes inevitable [38, 39]. This can be avoided if DNA is extracted from serial sections with verification of villous in one hematoxylin-eosin-stained section . In addition, washing the specimen with sterile saline rather than any other liquid better preserves the DNA contents. There is still a shortage of ancillary examinations, especially genetic testing, in cases with a vesicular placenta [15, 35, 41,42,43,44]. Thus, ancillary examinations should be recommended for a refined diagnosis.
If prenatal ultrasound detects a vesicular placenta coexisting with a fetus, patients should be referred to a fetal medicine unit. In this setting, patient evaluation should cover basic checkups, especially maternal serum HCG and alpha-fetoprotein (AFP) levels, thyroid hormones, blood pressure, and ultrasound. Meticulous ultrasound evaluation of fetal anatomical structures, placenta, and adnexa should be performed. If the molar placenta is clearly separated from the normal placenta, a diagnosis of twin pregnancy can be made (proposed scheme shown in Fig. 5); if there is one vesicular placenta, there is low specificity of ultrasound diagnosis, as was observed in the present case. In addition, an invasive prenatal diagnosis (metaphase chromosome analysis and chromosomal microarray analysis) should be performed to confirm the fetal karyotype. Maternal cell-free DNA screening is an additional investigation to analyze placental genetic components or a potential alternative to invasive prenatal testing .
Even with normal fetal testing results, patients should be fully informed of the pros and cons of continuing the pregnancy. According to a recent meta-analysis of twin pregnancies with a complete mole and coexistent normal fetus, there are 50% chances of a live birth if the pregnancy is continued; the incidence of complications is 70.5% for vaginal bleeding, 40.1% for intrauterine fetal death, 39% for preterm births, 34% for GTN, 23.3% for hyperthyroidism and 14.3% for preeclampsia . Other possible complications of hydatidiform moles are fetal growth restriction, hyperemesis, theca lutein cyst, and fetal-maternal hemorrhage [12, 20]. The risk of GTN does not increase with advancing gestational age , but opinions vary regarding the risk of GTN following a twin pregnancy with a hydatidiform mole versus that after a singleton complete mole. Some have reported similar risk while others have reported a higher risk for the former [20, 47]. Mosaic complete or partial moles probably share these complications with common hydatidiform moles. In a systematic review of cases of PMD, preterm delivery, FGR, and intrauterine fetal death affected 52, 33 and 13% of PMD patients .
In the absence of any severe complication necessitating termination of pregnancy and if the patient opts for expectant management, close prenatal monitoring for potential complications and serial ultrasound examinations should be carried out. If there are severe complications or patient chooses to terminate, the methods for pregnancy termination depend on the gestational age. Suction curettage with ultrasound guidance is recommended in early pregnancy. Plans for second-trimester termination should be made according to the patient’s condition and local guidelines. There is no clear consensus on the risks of GTN following different abortion or delivery methods; however, some argue against medical abortion and vaginal delivery due to potential risk of metastasis of trophoblastic cells by uterine contractions [7, 41, 42, 48]. Thus, cesarean section is recommended to deliver a viable fetus. For patients with a hydatidiform mole, regular follow-up should be followed as per guidelines [7, 49].
A strength of our report is that this is the first recorded case of twin pregnancy with a partial mole, with the two placentas displaying an intermixed pattern. We find that there is still room for refined diagnosis in obstetrical molar cases. A limitation of our report is that we could not obtain a satisfactory genotyping result of the molar tissue. Given the limited evidence in our case and the literature, further studies are required to focus on the diagnosis and molecular genotyping in cases of vesicular placenta coexisting with a fetus, genetic basis of PMD, the risk of GTN following a twin pregnancy with hydatidiform mole compared with the risk following a singleton mole, and the risk of GTN following different modes of pregnancy termination or delivery.
In conclusion, this report describes a rare case of a twin pregnancy comprising a partial mole that presented as a singleton mole in prenatal imaging. Coexistence of a vesicular placenta with a fetus is a complex scenario which is tricky to manage. A comprehensive evaluation of maternal-fetal state, including prenatal imaging, fetal genetic testing, and maternal complication screening is required to individualize the management. Selective use of p57KIP2 immunohistochemical staining, FISH, or DNA genotyping is strongly recommended to refine diagnosis in addition to placental routine microscopic evaluation.
Availability of data and materials
The datasets of the current study are not publicly available due to protection of the patient’s privacy but are available from the corresponding author on reasonable request.
Placental mesenchymal dysplasia
Human chorionic gonadotropin
Confined placental mosaicism
Fetal growth restriction
Gestational trophoblastic neoplasia
In vitro fertilization
Magnetic resonance imaging
Short tandem repeat
Fluorescence in situ hybridization
Etoposide, methotrexate, actinomycin D, cyclophosphamide, vincristine [oncovin]
Small for gestational age
Chromosome enumeration probes
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Partial financial support was received from the National Natural Science Foundation of China (Grant number 81741015) and the Natural Science Foundation of Guangdong Province (Grant number 2018A030313832).
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The study was approved by the Ethics Committee of the First Affiliated Hospital of Sun Yat-Sen University (Approval number: 226).
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Lin, M., Chen, J., Liao, B. et al. When a vesicular placenta meets a live fetus: case report of twin pregnancy with a partial hydatidiform mole. BMC Pregnancy Childbirth 21, 694 (2021). https://doi.org/10.1186/s12884-021-04160-2
- Twin pregnancy
- Hydatidiform mole
- Placental mesenchymal dysplasia
- Case report