Gadgil Nisha, McClugage Samuel G, Aldave Guillermo, Bauer David F, Weiner Howard L, Huisman Thierry A G M, Sanz-Cortes Magdalena, Belfort Michael A, Emrick Lisa, Clark Gary, Joyeux Luc, Whitehead William E
1Department of Neurosurgery, Baylor College of Medicine/Texas Children's Hospital, Houston.
2Edward B. Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston.
J Neurosurg Pediatr. 2022 Jul 22;30(3):342-348. doi: 10.3171/2022.6.PEDS22102. Print 2022 Sep 1.
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.
胎儿后颅膨出(脑脊膜膨出和脑膨出)的宫内修复手术是基于胎儿手术可防止孕期神经组织渐进性疝出及脑损伤这一前提进行的。然而,孕期,尤其是从产前诊断到产后,神经组织渐进性疝出的程度尚不清楚。本研究的目的是描述胎儿颅膨出患者的自然病史,重点关注渐进性疝出的发生率。
作者对2006年至2021年间转诊至其中心的所有胎儿后颅膨出患者进行了一项回顾性队列研究。所有患者均接受了产前和产后MRI检查。渐进性疝出(主要结局)定义为颅膨出内神经组织绝对体积增加>5%或关键结构新疝入颅膨出。计算全脑和颅膨出体积,以确定从产前到产后MRI的疝出进展情况。在1岁时收集有关脑积水、癫痫和发育迟缓(次要结局)的信息。
20例患者符合所有研究标准。10例患者(50%;95%CI 0.27 - 0.73)从产前到产后MRI显示有渐进性疝出。3例有渐进性疝出的患者产前诊断为脑脊膜膨出,产后诊断为脑膨出。2例无进展的患者产前诊断为脑脊膜膨出,出生时已消退并闭锁。产前小脑扁桃体疝(p = 0.03)和产前小头畸形(p = 0.05)均为渐进性疝出的预测因素。在本研究中,脑积水(44%)、癫痫(44%)和发育迟缓(63%)的发生率与渐进性疝出的发生无关。
在本研究中,渐进性疝出并非罕见事件(50%)。胎儿小脑扁桃体疝和胎儿小头畸形与渐进性疝出的发生有关。这些结果支持进一步研究宫内渐进性疝出发生的原因,以及宫内渐进性脑疝在决定临床结局方面是否起重要作用。