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产前诊断脑裂畸形的胎儿磁共振成像表现、病因及结局

Fetal MRI Findings, Etiology, and Outcome in Prenatally Diagnosed Schizencephaly.

作者信息

George Elizabeth, Vassar Rachel, Yu Yolanda, Norton Mary E, Gano Dawn, Glenn Orit A

机构信息

From the Department of Radiology and Biomedical Imaging (E.G., O.A.G), University of California, San Francisco, California

Department of Neurology (R.V. D.G.), University of California, San Francisco, California.

出版信息

AJNR Am J Neuroradiol. 2025 Apr 2;46(4):800-807. doi: 10.3174/ajnr.A8523.

Abstract

BACKGROUND AND PURPOSE

Schizencephaly is a rare brain anomaly that is increasingly detected in utero. There are limited data on the etiology and outcomes in fetal schizencephaly to guide work-up and counseling. We aimed to determine the associated imaging findings, etiology, and outcomes in schizencephaly detected in utero.

MATERIALS AND METHODS

This retrospective cohort study included 22 fetuses with a total of 34 schizencephaly defects identified by keyword search of fetal MRI reports from 1996 to 2022 followed by image review. Follow-up fetal and postnatal imaging, when available, was reviewed. Data on demographics, etiology, and outcomes were extracted from the electronic medical record.

RESULTS

The schizencephaly defect was open in 28/34, most common in the MCA territory (23/34), and commonly involved the frontal lobe (16/34). Additional intracranial abnormalities were seen in all fetuses, including other cortical malformations (13/22), abnormal posterior fossa (12/22), abnormal corpus callosum (10/20), and intraparenchymal hemorrhage (9/22). The cause of schizencephaly was classified as secondary (as evidenced by intraparenchymal hemorrhage at schizencephaly, monochorionic twin gestation, infection, or maternal/placental risk factor) in 64% (14/22), potentially genetic in 9% (2/22), and unknown in 27% (6/22). Among those liveborn ( = 8), we observed the following outcomes: postnatal death (1/8), tube feeding (1/7), shunted hydrocephalus (1/7), and epilepsy (4/7). Among those older than 1 year of age, cerebral palsy (4/5) and speech delay or intellectual disability (3/5) were common. Cortical malformations remote from schizencephaly were associated with epilepsy ( = .03). On postnatal imaging, open defects were often involuted (8/11), and there were high rates of new/additional findings (4/6).

CONCLUSIONS

In this cohort, fetal schizencephaly was always associated with additional intracranial abnormalities. In most cases, there was evidence that schizencephaly was likely secondary to prior injury. Imaging characteristics may provide clues regarding neurodevelopmental outcome. Postnatal imaging is crucial in assessing the evolution as well as detection of additional abnormalities.

摘要

背景与目的

脑裂畸形是一种罕见的脑部异常,在子宫内越来越多地被检测到。关于胎儿脑裂畸形的病因和预后的数据有限,难以指导检查和咨询工作。我们旨在确定子宫内检测到的脑裂畸形的相关影像学表现、病因和预后。

材料与方法

这项回顾性队列研究纳入了22例胎儿,通过对1996年至2022年胎儿MRI报告进行关键词搜索,随后进行图像审查,共识别出34处脑裂畸形缺陷。如有可用的随访胎儿及产后影像学资料,也进行了审查。从电子病历中提取人口统计学、病因和预后数据。

结果

34处脑裂畸形缺陷中28处为开放性,最常见于大脑中动脉供血区(34处中的23处),且常累及额叶(34处中的16处)。所有胎儿均可见其他颅内异常,包括其他皮质畸形(22例中的13例)、后颅窝异常(22例中的12例)、胼胝体异常(20例中的10例)和脑实质内出血(22例中的9例)。脑裂畸形的病因分类如下:64%(22例中的14例)为继发性(脑裂畸形处脑实质内出血、单绒毛膜双胎妊娠、感染或母体/胎盘危险因素可证实),9%(22例中的2例)可能为遗传性,27%(22例中的6例)病因不明。在存活出生的胎儿中(n = 8),我们观察到以下结局:产后死亡(8例中的1例)、鼻饲(7例中的1例)、分流性脑积水(7例中的1例)和癫痫(7例中的4例)。在1岁以上的儿童中,脑性瘫痪(5例中的4例)和语言发育迟缓或智力残疾(5例中的3例)很常见。远离脑裂畸形的皮质畸形与癫痫相关(P = .03)。产后影像学检查显示,开放性缺陷常已愈合(11例中的8例),且新发现/额外发现的发生率较高(6例中的4例)。

结论

在该队列中,胎儿脑裂畸形总是与其他颅内异常相关。在大多数情况下有证据表明脑裂畸形可能继发于先前的损伤。影像学特征可能为神经发育结局提供线索。产后影像学检查对于评估病情演变以及发现其他异常至关重要。

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