Role of prenatal magnetic resonance imaging in fetuses with isolated anomalies of corpus callosum: multinational study

Filomena Giulia Sileo, Gianluigi Pilu, Daniela Prayer, Giuseppe Rizzo, Asma Khalil, Lucia Managanaro, Paolo Volpe, Tim Van Mieghem, Emma Bertucci, José Morales Roselló, Fabio Facchinetti, Daniele Di Mascio, Tamara Stampalija, Danilo Buca, Sara Tinari, Ludovica Oronzi, Giada Ercolani, Alice D’Amico, Adele D'Amico, Barbara MatarrelliChiara Cerra, Ilaria Fantasia, Lucia Pasquini, Giulia Masini, Claudiana Olivieri, Tullio Ghi, Tiziana Frusca, Andrea Dall’Asta, Silvia Visentin, Erich Cosmi, Ignazio D’Errico, Cecilia Villalain, Olivia Mendez Quintero, Antonella Giancotti, Valentina D’Ambrosio, Amanda Antonelli, Massimo Caulo, Valentina Panar, Marco De Santis, Ilenia Mappa, Federico Prefumo, Lorenzo Pinelli, Gabriela Loscalzo, Gabriella Bracalente, Giada Bracalente, Marco Liberati, Elisa Filippi, Elena Trincia, Petra Pateisky, Herbert Kiss, Joana Curado, Marta Almeida, Antonia Santos, Alberto Galindo, Francesco D’Antonio, Francesco D'Antonio

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Objective: To assess the performance of fetal magnetic resonance imaging (MRI) in detecting associated anomalies in fetuses diagnosed with isolated corpus callosal (CC) anomaly on multiplanar ultrasound evaluation of the fetal brain (neurosonography). Methods: This was a multicenter, retrospective cohort study involving 14 fetal medicine centers in Italy, UK, Portugal, Canada, Austria and Spain. Inclusion criteria were fetuses with an apparently isolated CC anomaly, defined as an anomaly of the CC and no other additional central nervous system (CNS) or extra-CNS abnormality detected on expert ultrasound, including multiplanar neurosonography; normal karyotype; maternal age ≥ 18 years; and gestational age at diagnosis ≥ 18 weeks. The primary outcome was the rate of additional CNS abnormalities detected exclusively on fetal MRI within 2 weeks following neurosonography. The secondary outcomes were the rate of additional abnormalities according to the type of CC abnormality (complete (cACC) or partial (pACC) agenesis of the CC) and the rate of additional anomalies detected only on postnatal imaging or at postmortem examination. Results: A total of 269 fetuses with a sonographic prenatal diagnosis of apparently isolated CC anomalies (207 with cACC and 62 with pACC) were included in the analysis. Additional structural anomalies of the CNS were detected exclusively on prenatal MRI in 11.2% (30/269) of cases, with malformations of cortical development representing the most common type of anomaly. When stratifying the analysis according to the type of CC anomaly, the rate of associated anomalies detected exclusively on MRI was 11.6% (24/207) in cACC cases and 9.7% (6/62) in pACC cases. On multivariate logistic regression analysis, only maternal body mass index was associated independently with the likelihood of detecting associated anomalies on MRI (odds ratio, 1.07 (95% CI, 1.01–1.14); P = 0.03). Associated anomalies were detected exclusively after delivery and were missed on both types of prenatal imaging in 3.9% (8/205) of fetuses with prenatal diagnosis of isolated anomaly of the CC. Conclusion: In fetuses with isolated anomaly of the CC diagnosed on antenatal neurosonography, MRI can identify a small proportion of additional anomalies, mainly malformations of cortical development, which are not detected on ultrasound. © 2021 International Society of Ultrasound in Obstetrics and Gynecology.
Lingua originaleEnglish
pagine (da-a)26-33
Numero di pagine8
RivistaUltrasound in Obstetrics and Gynecology
Volume58
DOI
Stato di pubblicazionePubblicato - 2021

Keywords

  • MRI
  • central nervous system
  • corpus callosum
  • prenatal diagnosis
  • fetal ultrasound
  • neurosonography
  • fetal magnetic resonance imaging

Fingerprint

Entra nei temi di ricerca di 'Role of prenatal magnetic resonance imaging in fetuses with isolated anomalies of corpus callosum: multinational study'. Insieme formano una fingerprint unica.

Cita questo