Position of the choroid plexus of the fourth ventricle in first‐ and second‐trimester fetuses: a novel approach to early diagnosis of cystic posterior fossa anomalies

ABSTRACT Objective To describe the sonographic appearance and position of the choroid plexus of the fourth ventricle (4V‐CP) between 12 and 21 weeks' gestation in normal fetuses and in fetuses with Dandy–Walker malformation (DWM) or Blake's pouch cyst (BPC). Methods The study population co...

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Veröffentlicht in:Ultrasound in obstetrics & gynecology 2021-10, Vol.58 (4), p.568-575
Hauptverfasser: Volpe, P., De Robertis, V., Volpe, G., Boito, S., Fanelli, T., Olivieri, C., Votino, C., Persico, N.
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Sprache:eng
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Zusammenfassung:ABSTRACT Objective To describe the sonographic appearance and position of the choroid plexus of the fourth ventricle (4V‐CP) between 12 and 21 weeks' gestation in normal fetuses and in fetuses with Dandy–Walker malformation (DWM) or Blake's pouch cyst (BPC). Methods The study population comprised 90 prospectively recruited normal singleton pregnancies and 41 pregnancies identified retrospectively from our institutional database that had a suspected posterior fossa anomaly at 12–13 weeks' gestation based on the ultrasound finding of abnormal hindbrain spaces. In all cases the final diagnosis was confirmed by prenatal and/or postnatal magnetic resonance imaging or postmortem examination. All pregnancies underwent a detailed ultrasound assessment, including a dedicated examination of the posterior fossa, at 12–13 weeks, 15–16 weeks and 20–21 weeks of gestation. Two‐dimensional ultrasound images of the midsagittal and coronal views of the brain through the posterior fontanelle and three‐dimensional volume datasets were obtained. Multiplanar orthogonal image correlation with volume contrast imaging was used as the reference visualization mode. Two independent operators, blinded to the fetal outcome, were asked to classify the 4V‐CP as visible or not visible in both normal and abnormal cases, and to assess if the 4V‐CP was positioned inside or outside the cyst in fetuses with DWM and BPC. Results Of the 41 fetuses with apparently isolated cystic posterior fossa anomaly in the first trimester, eight were diagnosed with DWM, 29 were diagnosed with BPC and four were found to be normal in the second trimester. The position of the 4V‐CP differed between DWM, BPC and normal cases in the first‐ and second‐trimester ultrasound examinations. In particular, in normal fetuses, no cyst was present and, in the midsagittal and coronal planes of the posterior fossa, the 4V‐CP appeared as an echogenic oval‐shaped structure located inside the 4V apparently attached to the cerebellar vermis. In fetuses with DWM, the 4V‐CP was not visible in the midsagittal view because it was displaced inferolaterally by the cyst. In contrast, in the coronal view of the posterior brain, the 4V‐CP was visualized in all cases with DWM at 12–13 weeks, with a moderate decrease in the visualization rate at 15–16 weeks (87.5%) and at 20–21 weeks (75%). In the coronal view, the 4V‐CP was classified as being outside the cyst in all DWM cases at 12–13 weeks and in 87.5% and 75% of cases at 15–16 and 20–21
ISSN:0960-7692
1469-0705
DOI:10.1002/uog.23651