Natural history of posterior fetal cephaloceles and incidence of progressive cephalocele herniation.

congenital fetal surgery occipital encephalocele

Journal

Journal of neurosurgery. Pediatrics
ISSN: 1933-0715
Titre abrégé: J Neurosurg Pediatr
Pays: United States
ID NLM: 101463759

Informations de publication

Date de publication:
22 Jul 2022
Historique:
received: 22 03 2022
accepted: 16 06 2022
entrez: 28 7 2022
pubmed: 29 7 2022
medline: 29 7 2022
Statut: aheadofprint

Résumé

In utero repair of fetal posterior cephaloceles (meningocele and encephalocele) is being performed based on the premise that fetal surgery prevents progressive herniation of neural tissue and brain damage during pregnancy. However, the extent to which progressive herniation occurs during pregnancy, specifically from prenatal diagnosis to after delivery, is not well known. The objective of this study was to describe the natural history of patients with fetal cephaloceles focusing on the incidence of progressive herniation. The authors conducted a retrospective cohort study of all patients referred to their center for posterior fetal cephalocele between 2006 and 2021. All patients underwent prenatal and postnatal MRI. Progressive herniation (primary outcome) was defined as an increase in the absolute volume of neural tissue within the cephalocele of > 5% or new herniation of a critical structure into the cephalocele. Total brain and cephalocele volumes were calculated to determine herniation progression from prenatal to postnatal MRI. Information on the presence of hydrocephalus, epilepsy, and developmental delay (secondary outcomes) was collected at 1 year of age. Twenty patients met all study criteria. Ten patients (50%; 95% CI 0.27-0.73) demonstrated progressive herniation from prenatal to postnatal MRI. Three patients with progressive herniation were diagnosed with a meningocele prenatally and had an encephalocele postnatally. Two patients without progression had meningocele identified prenatally that regressed and became atretic by birth. Both prenatal hindbrain herniation (p = 0.03) and prenatal microcephaly (p = 0.05) were predictive of progressive herniation. The rates of hydrocephalus (44%), epilepsy (44%), and developmental delay (63%) were not associated with the occurrence of progressive herniation in this study. In this study, progressive herniation was not a rare event (50%). Fetal hindbrain herniation and fetal microcephaly were associated with the occurrence of progressive herniation. These results support further investigations into why progressive herniation occurs in utero and if progressive cerebral herniation in utero plays a significant role in determining clinical outcome.

Identifiants

pubmed: 35901680
doi: 10.3171/2022.6.PEDS22102
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Auteurs

Nisha Gadgil (N)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.

Samuel G McClugage (SG)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.

Guillermo Aldave (G)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.

David F Bauer (DF)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.

Howard L Weiner (HL)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.

Thierry A G M Huisman (TAGM)

2Edward B. Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston.

Magdalena Sanz-Cortes (M)

3Department of Obstetrics and Gynecology, Baylor College of Medicine and Texas Children's Hospital Pavilion for Women, Houston.

Michael A Belfort (MA)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.
3Department of Obstetrics and Gynecology, Baylor College of Medicine and Texas Children's Hospital Pavilion for Women, Houston.

Lisa Emrick (L)

4Department of Pediatric Neurology, Baylor College of Medicine, Houston; and.

Gary Clark (G)

4Department of Pediatric Neurology, Baylor College of Medicine, Houston; and.

Luc Joyeux (L)

5Department of Pediatric Surgery, Texas Children's Hospital and Baylor College of Medicine, Houston, Texas.

William E Whitehead (WE)

1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.

Classifications MeSH