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Published in: Child's Nervous System 7/2020

01-07-2020 | Magnetic Resonance Imaging | Original Article

Brain abnormalities in myelomeningocele patients

Authors: Bárbara Albuquerque Morais, Davi Jorge Fontoura Solla, Vitor Nagai Yamaki, Suely Fazio Ferraciolli, Cesar Augusto P.F. Alves, Daniel Dante Cardeal, Hamilton Matushita, Manoel Jacobsen Teixeira

Published in: Child's Nervous System | Issue 7/2020

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Abstract

Background

Myelomeningocele (MMC) is often related to hydrocephalus and Chiari malformation (CM) type 2; however, other brain abnormalities have been reported in this population. In order to better understand and quantify other forebrain abnormalities, we analyzed magnetic resonance imaging (MRI) of MMC patients treated in utero or postnatal.

Methods

Between January 2014 and March 2017, 59 MMC were treated in our hospital. Thirty-seven patients (32 postnatal and 5 intrautero repair) had brain MRI and were enrolled at the study. MRI was analyzed by two experienced neuroradiologists to identify the supra and infratentorial brain abnormalities.

Results

A wide range of brain abnormalities was consistently identified in MMC patients. As expected, the most common were hydrocephalus (94.5%) and CM type II (89.1%). Of note, we found high incidence of corpus callosum abnormalities (86.4%), mostly represented by dysplasia (46%).

Conclusions

The data are consistent with the concept that brain abnormalities related to MMC can be both infratentorial and supratentorial, cortical, and subcortical. More studies are needed to correlate these forebrain abnormalities to long-term functional outcome and their prognostic value for these patients.
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Metadata
Title
Brain abnormalities in myelomeningocele patients
Authors
Bárbara Albuquerque Morais
Davi Jorge Fontoura Solla
Vitor Nagai Yamaki
Suely Fazio Ferraciolli
Cesar Augusto P.F. Alves
Daniel Dante Cardeal
Hamilton Matushita
Manoel Jacobsen Teixeira
Publication date
01-07-2020
Publisher
Springer Berlin Heidelberg
Published in
Child's Nervous System / Issue 7/2020
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-019-04386-8

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