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New insights in cerebral findings associated with fetal myelomeningocele: a retrospective cohort study in a single tertiary centre

Authors :
Catherine Garel
Juliette Garel
Paul Maurice
Ferdinand Dhombres
Lucie Guilbaud
Stéphanie Friszer
Emeline Maisonneuve
H. Ducou Le Pointe
J.-M. Jouannic
Eléonore Blondiaux
Service de Médecine Fœtale [CHU Trousseau]
CHU Trousseau [APHP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Source :
BJOG: An International Journal of Obstetrics and Gynaecology, BJOG: An International Journal of Obstetrics and Gynaecology, Wiley, 2021, 128 (2), pp.376-383. ⟨10.1111/1471-0528.16185⟩
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

Abstract

International audience; Objective: To investigate cerebral anomalies other than Chiari type 2 malformation in fetuses with myelomeningocele (MMC).Design: A retrospective cohort study in a single tertiary centre.Setting: A review of associated cerebral anomalies in cases with prenatal diagnosis of myelomeningocele.Population: Seventy cases of fetal myelomeningocele.Methods: Ultrasound and MRI images were blindly reviewed. Postnatal imaging and results of the postmortem results were also reviewed. The association between cerebral anomalies and the following ultrasound findings was measured: level of the defect, ventriculomegaly, microcephaly and fetal talipes.Main outcome measures: A microcephaly was observed in 32/70 cases (46%) and a ventriculomegaly was observed in 39/70 cases (56%). Other cerebral anomalies were diagnosed in 47/70 (67%).Results: Other cerebral anomalies were represented by 42/70 cases with abnormal CC (60%), 8/70 cases with perinodular heterotopia (PNH; 11%), 2/70 cases with abnormal gyration (3%). MRI performed only in fetal surgery cases confirmed the ulltrasound findings in all cases and provided additional findings in two cases (PNH). Risk ratios of fetal cerebral anomalies associated with MMC did not reach significance for microcephaly, ventriculomegaly, talipes or the level of the defect There was an overall good correlation between pre- and postnatal findings with a Kappa value of 0.79 [95% CI 0.57-1] and 82% agreement.Conclusion: Fetal brain anomalies other than Chiari type 2 malformation are frequently observed in fetuses with myelomeningocele, predominantly represented by CC anomalies. Whether these associated cerebral anomalies have an impact on selecting cases eligible for fetal surgery needs further evaluation.Tweetable abstract: Fetal cerebral anomalies other than Chiari type 2 malformation, microcephaly, and ventriculomegaly may be associated with MMC in up to 67% of the cases.

Details

Language :
English
ISSN :
14700328 and 14710528
Database :
OpenAIRE
Journal :
BJOG: An International Journal of Obstetrics and Gynaecology, BJOG: An International Journal of Obstetrics and Gynaecology, Wiley, 2021, 128 (2), pp.376-383. ⟨10.1111/1471-0528.16185⟩
Accession number :
edsair.doi.dedup.....98a319ef4da7652fff48436f05c26639
Full Text :
https://doi.org/10.1111/1471-0528.16185⟩