In utero progression of cephaloceles: prenatal to postnatal analysis.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY
Maria A Punchak, Sanjana R Salwi, Sierra D Land, Sarah Hamimi, Tom A Reynolds, Jordan W Swanson, Jesse A Taylor, Christina Paidas Teefey, Juliana S Gebb, Nahla Khalek, Shelly Soni, Julie S Moldenhauer, N Scott Adzick, Gregory G Heuer, Tracy M Flanders
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Abstract

Objective: The natural history of cephaloceles is not well understood. The goal of this study was to better understand the natural history of fetal cephaloceles from prenatal diagnosis to the postnatal period.

Methods: Between January 2013 and April 2023, all patients evaluated with a cephalocele at the Center for Fetal Diagnosis and Treatment were identified. All patients underwent prenatal and postnatal MRI. Demographic and imaging covariates were obtained from the electronic medical record. Volumetric analyses were performed to determine the percentage of neural tissue within the cephalocele. Progressive herniation was defined as an increase in cephalocele absolute neural tissue volume ≥ 5% or new herniation of an additional intracranial structure into the cephalocele.

Results: A total of 25 patients met the inclusion criteria. Of these patients, 6 (24%) exhibited progressive cephalocele herniation from the prenatal to postnatal MRI. The median sac volume was 2.2 mL (mean 6.2 mL, range 0.3-40.5 mL). The median change in brain volume in the patients with cephalocele progression was a decrease of 1.5% (mean -7.3%, range -36.4% to 3.1%). Cephalocele sac volume at the time of fetal imaging was predictive of progressive herniation, which persisted on multivariate analysis when controlling for gestational age, sex, and percentage of herniated neural tissue. While 44% of the patients had ventriculomegaly, 56% ultimately required permanent CSF diversion.

Conclusions: Progressive neural herniation from the fetal to postnatal period is not commonly seen in fetal cephaloceles. Sac volume is associated with an increased risk of progressive herniation into the cephalocele.

胎儿畸形的宫内进展:产前产后分析。
目的:脑积水的自然史尚不清楚。本研究的目的是为了更好地了解胎儿头膨出的自然历史,从产前诊断到产后。方法:在2013年1月至2023年4月期间,在胎儿诊断和治疗中心确定了所有被评估为头膨出的患者。所有患者均进行了产前和产后MRI检查。从电子病历中获得人口统计学和影像学协变量。进行体积分析以确定脑膨出内神经组织的百分比。进行性疝被定义为头膨出绝对神经组织体积增加≥5%或新的颅内结构突出到头膨出。结果:25例患者符合纳入标准。在这些患者中,6例(24%)从产前到产后MRI表现为进行性脑膨出。囊体积中位数为2.2 mL(平均6.2 mL,范围0.3-40.5 mL)。头膨出进展患者的中位脑容量变化减少1.5%(平均-7.3%,范围-36.4%至3.1%)。胎儿成像时的头膨出囊体积可预测进行性疝,在控制胎龄、性别和疝出神经组织百分比的多变量分析中,这一预测仍然存在。44%的患者有脑室肿大,56%的患者最终需要永久性脑脊液分流。结论:从胎儿期到产后的进行性神经疝在胎儿头膨出中并不常见。囊体积与进行性疝入头膨出的风险增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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