IMAGING FOR RESIDENTS – QUIZ
Year : 2020 | Volume
: 28 | Issue : 4 | Page : 275--277
Abnormal fetal profile at first-trimester ultrasound scan complicated by severe polyhydramnios at the second half of pregnancy
Ana Portela Carvalho, Catarina Estevinho, Maria Coelho, Juliana Rocha, Carla Marinho, Graça Rodrigues
Department of Obstetrics and Gynaecology, Centro Hospitalar do Tâmega e Sousa, Penafiel, Porto, Portugal
Correspondence Address:
Dr. Ana Portela Carvalho
Department of Obstetrics and Gynaecology, Centro Hospitalar do Tâmega e Sousa, Avenida do Hospital Padre Américo, No. 210, 4564-007, Penafiel, Porto
Portugal
How to cite this article:
Carvalho AP, Estevinho C, Coelho M, Rocha J, Marinho C, Rodrigues G. Abnormal fetal profile at first-trimester ultrasound scan complicated by severe polyhydramnios at the second half of pregnancy.J Med Ultrasound 2020;28:275-277
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How to cite this URL:
Carvalho AP, Estevinho C, Coelho M, Rocha J, Marinho C, Rodrigues G. Abnormal fetal profile at first-trimester ultrasound scan complicated by severe polyhydramnios at the second half of pregnancy. J Med Ultrasound [serial online] 2020 [cited 2023 Apr 1 ];28:275-277
Available from: http://www.jmuonline.org/text.asp?2020/28/4/275/276969 |
Full Text
Section 1 – Quiz
Case Description
A 37-year-old pregnant woman, multigravida (G3P1), was referred to our outpatient clinic at 9 weeks of gestation. The first pregnancy was uneventful, and in the second pregnancy, the couple decided for medical termination of pregnancy at 16 weeks of gestation because of prenatal cytogenetic diagnosis of trisomy 21.
In the third pregnancy, the first-trimester ultrasound revealed a fetus with a crown-rump length of 63.4 mm (gestational age of 12 weeks and 6 days) and a nuchal translucency of 1.70 mm (below the 95th centile), normal Doppler of ductus venosus, no tricuspid regurgitation, and present nasal bones. There was, however, a suspicion for fetal micrognathia [Figure 1] and [Figure 2]. Remaining morphology of the fetus was considered normal at this stage. The placenta was anterior, the umbilical cord had three vessels, and the amniotic fluid volume was normal. First trimester combined screening had reduced risk for aneuploidies: trisomy 21 (1:6260) and trisomies 18 and 13 (1:100,000) with pregnancy-associated plasma protein-A = 1.26 MoM and free beta-human chorionic gonadotropin = 1.50 MoM. Performance of invasive testing was offered, but the couple refused.{Figure 1}{Figure 2}
At the mid-trimester ultrasound scan, performed at 20 weeks and 5 days of gestation, the fetus had cephalic presentation, normal amniotic fluid index, and a right anterolateral placenta, with no relation with internal cervical os. Biometric parameters were adequate for gestational age. The skull configuration and intracranial structures were normal. Fetal facial profile was abnormal, suggesting mandibular hypoplasia and glossoptosis [Figure 3] and [Figure 4]. Nasal bones measured 7.5 mm (above the 5th centile) and morphology of the upper lip was considered normal [Figure 5]. Stomach bubble was visible. There were no spinal, thoracic, cardiac, abdominal, genitourinary, or limb abnormalities, and the fetus had normal masculine genitalia. Taking into consideration the persistent suspicion of microretrognathia, prenatal counseling was made again, and an amniocentesis was proposed to the couple that refused it.{Figure 3}{Figure 4}{Figure 5}
No other sonographic anomalies were identified until the third trimester. Screening for gestational diabetes was negative, and there was no evidence for maternal TORCH (Toxoplasmosis, Other [syphilis, varicella-zoster, parvovirus B19], Rubella, Cytomegalovirus, and Herpes infections) seroconversion or isoimmunization. Detailed fetal echocardiography was normal.
At 32 weeks and 5 days, ultrasound revealed a mild polyhydramnios with an amniotic fluid index of 24.5 cm and a deepest pocket of 8.9 cm. Estimated fetal weight was 2347 g, corresponding to the 82nd centile. Fetal Doppler and biophysical profile were normal.
Polyhydramnios was progressively increasing in severity. At 36 weeks, the fetus had an amniotic fluid index of 35.2 cm (deepest pool of 10.3 cm [Figure 6]) and an estimated fetal weight of 2942 g (61st centile). Fetal Doppler and biophysical profile were normal. Detailed review of fetal anatomy highlighted a prominent upper lip and receding chin in the mid-sagittal view of the face [Figure 7],[Figure 8],[Figure 9]. The patient was then hospitalized because of discomfort and dyspnea. A controlled induction of labor was initiated at 37 weeks. An emergent C-section was performed because of placental abruption after spontaneous membrane rupture. A male newborn weighing 2760 g and with Apgar index 5/7/8 was delivered and presented signs of airway obstruction. After birth, the newborn was evaluated by Pediatrics Surgery, Plastic Surgery, and Otorhinolaryngology. A complete soft palate cleft and glossoptosis were visualized in addition to the micrognathia prenatally diagnosed and no other morphologic anomalies were detected. The newborn karyotype and array comparative genomic hybridization were normal.{Figure 6}{Figure 7}{Figure 8}{Figure 9}
What Is the Diagnosis?
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
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Conflicts of interest
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