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脑裂畸形胎儿合并轻度脑室扩张:磁共振成像的作用。

Agenesis of the corpus callosum in fetuses with mild ventriculomegaly: role of MR imaging.

机构信息

Istituto di Radiologia, Università di Verona, Policlinico G.B. Rossi, P.le L.A. Scuro 10, 37134, Verona, Italy.

出版信息

Radiol Med. 2010 Mar;115(2):301-12. doi: 10.1007/s11547-009-0474-7. Epub 2009 Dec 16.

Abstract

PURPOSE

We evaluated the role of magnetic resonance (MR) imaging in the diagnosis of corpus callosum agenesis - isolated or associated with other anomalies - in fetuses with mild cerebral ventriculomegaly, as depicted at prenatal sonography.

MATERIAL AND METHODS

Between January 2005 and March 2007, 33 fetuses with a mean gestational age of 28.9 weeks (range 17-37) and mild ventriculomegaly diagnosed at prenatal sonography were included in this prospective study. All fetuses underwent MR imaging according to the following protocol: half-Fourier T2-weighted images along the three orthogonal plane according to the longitudinal axis of the mother, and subsequently three orthogonal planes were acquired according to the fetal brain. Quantitative image analysis included the size of the transverse diameter of the lateral ventricles, in the axial plane, and the thickness of the adjacent cerebral cortex. Qualitative image analysis included morphology of the lateral ventricles (normal, parallel pattern colpocephaly), signal intensity changes of the fetal brain, interruption of the germinative matrix, agenesis of the corpus callosum (complete/partial) and associated malformations. Postnatal physical examination and diagnostic imaging, as well as surgery, were the standard of diagnosis.

RESULTS

Mean axial diameter of the lateral ventricle was 11.6 mm (range 10-15 mm), and mean thickness of the adjacent cerebral cortex was 2.1 mm (range 1.8-3 mm); 23/33 fetuses (70%) showed normal morphology of the lateral ventricles, and 8/33 (24%) showed abnormal morphology (parallel pattern, colpocephaly). The entire corpus callosum was visualised in 20/33 fetuses (60%). In 8/33 fetuses (25%), partial agenesis was diagnosed, whereas in 5/33 (15%), there was hypogenesis. In 6/13 fetuses (46%), isolated corpus callosum agenesis was detected, and two cases of hypogenesis of the corpus callosum were misinterpreted - overestimated in one case and underestimated in another.

CONCLUSIONS

MR imaging may prove to be a useful second-line imaging modality in the prenatal diagnosis of corpus callosum agenesis in fetuses with mild ventriculomegaly.

摘要

目的

我们评估了磁共振(MR)成像在产前超声检查显示轻度脑室扩大的胎儿中诊断单纯性或伴发其他异常的胼胝体发育不全的作用。

材料与方法

2005 年 1 月至 2007 年 3 月间,我们前瞻性研究了 33 例胎儿,这些胎儿在产前超声检查时被诊断为平均胎龄 28.9 周(范围 17-37 周)的轻度脑室扩大。所有胎儿均按以下方案进行 MR 成像:沿母亲的纵轴进行半傅立叶 T2 加权图像,随后按胎儿大脑采集三个正交平面。定量图像分析包括轴位外侧脑室的横向直径大小,以及相邻脑皮质的厚度。定性图像分析包括侧脑室的形态(正常,平行模式尖颅畸形)、胎儿脑的信号强度变化、生发基质中断、胼胝体发育不全(完全/部分)和伴发畸形。新生儿体格检查、诊断性影像学检查以及手术是诊断的标准。

结果

平均侧脑室轴位直径为 11.6mm(范围 10-15mm),平均相邻脑皮质厚度为 2.1mm(范围 1.8-3mm);23/33 例(70%)胎儿的侧脑室形态正常,8/33 例(24%)胎儿的侧脑室形态异常(平行模式,尖颅畸形)。20/33 例胎儿(60%)可以完整显示胼胝体。8/33 例(25%)胎儿诊断为部分发育不全,5/33 例(15%)胎儿为发育不良。13 例胎儿中有 6 例(46%)孤立性胼胝体发育不全,2 例胼胝体发育不良被误诊——1 例高估,1 例低估。

结论

MR 成像可能成为产前诊断轻度脑室扩大胎儿胼胝体发育不全的有用二线影像学方法。

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