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The Role of Fetal MRI for Suspected Anomalies of the Posterior Fossa - 24/03/21

Doi : 10.1016/j.pediatrneurol.2021.01.002 
Sarah D. Schlatterer, MD, PhD a, b, c, , Laura Sanapo, MD, MSHS, RDMS d, e, Adre J. du Plessis, MBChB, MPH a, b, c, Matthew T. Whitehead, MD f, g, Sarah B. Mulkey, MD, PhD a, b, c
a Prenatal Pediatrics Institute, Children’s National Hospital, Washington, District of Columbia 
b Department of Neurology, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia 
c Department of Pediatrics, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia 
d Women’s Medicine Collaborative-Division of Research, The Miriam Hospital, Providence, Rhode Island 
e Department of Medicine, The Warren Alpert Medical School of Brown University, Providence, Rhode Island 
f Department of Neuroradiology, Children’s National Hospital, Washington, District of Columbia 
g Department of Radiology, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia 

Communications should be addressed to: Dr. Schlatterer; Prenatal Pediatrics Institute; Children’s National Hospital; 111 Michigan Ave NW, Suite 3118; Washington, DC, 20010.Prenatal Pediatrics InstituteChildren’s National Hospital111 Michigan Ave NWSuite 3118WashingtonDC20010

Abstract

Background

Posterior fossa anomalies can be diagnostic dilemmas during the fetal period. The prognosis for different diagnoses of the posterior fossa varies widely. We investigated whether fetal magnetic resonance imaging (MRI) and prenatal neurology consultation led to an alternate prognosis for fetuses referred due to concern for a fetal posterior fossa anomaly and concordance between pre- and postnatal diagnoses.

Methods

This is a retrospective study of cases referred to the Prenatal Pediatrics Institute at Children’s National Hospital from January 2012 to June 2018 due to concern for posterior fossa anomaly. Each encounter was scored for change in prognosis based upon clinical and fetal MRI report. Postnatal imaging was compared with prenatal imaging when available.

Results

In total, 180 cases were referred for fetal posterior fossa anomalies based on outside obstetric ultrasound and had both fetal MRI and a neurology consultation. Fetal MRI and neurology consultation resulted in a change in fetal prognosis in 70% of cases. The most common referral diagnosis in our cohort was Dandy-Walker continuum, but it was not often confirmed by fetal MRI. In complex cases, posterior fossa diagnosis and prognosis determined by fetal MRI impacted choices regarding pregnancy management. Postnatal imaging was obtained in 57 (47%) live-born infants. Fetal and postnatal prognoses were similar in 60%.

Conclusions

Fetal diagnosis affects pregnancy management decisions. The fetal-postnatal imaging agreement of 60% highlights the conundrum of balancing the timing of fetal MRI to provide the most accurate diagnosis of the posterior fossa abnormalities in time to make pregnancy management decisions.

Le texte complet de cet article est disponible en PDF.

Keywords : Congenital brain abnormality, Posterior fossa, Fetal neurology, Dandy-Walker malformation, Blake pouch cyst, Prenatal imaging, Vermis hypoplasia


Plan


 Author Contributions: Dr. Schlatterer designed the study, acquired and analyzed data, scored cases for prognosis, and drafted the manuscript. Dr. Sanapo participated in study design, discussion, and manuscript revision. Dr. du Plessis participated in conception and study design. Dr. Whitehead reviewed MRI images and participated in study design and manuscript revision. Dr. Mulkey designed the study, scored cases for prognosis, and drafted the manuscript with Dr. Schlatterer.
 Conflicts of Interest: The authors have no conflicts of interest to report.


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Vol 117

P. 10-18 - avril 2021 Retour au numéro
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