Guo W Y, Chang C Y, Ho D M, Wong T T, Sheu M H, Cheng H C, Chen S J, Hung J H
Department of Radiology, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taiwan, Republic of China.
Childs Nerv Syst. 2001 Sep;17(9):512-8. doi: 10.1007/s003810100471.
We used MR after sonography to help us in prenatal counseling in 58 complicated pregnancies from 1998 to 2000.
All fetal MR examinations were undertaken with a 1.5-T magnet using a body-phased-array coil and an ultrafast imaging technique, half-Fourier single-shot turbo spin-echo (HASTE). Twelve fetuses were found to have major anomalies, and in each of these cases either delivery was induced or the pregnancy was terminated. In 6 of the fetuses, with anomalies of the central nervous system, postmortem examinations were then performed after they failed to survive, and these constitute the patient sample investigated in the current study. The fetal gestational ages in these 6 cases ranged from 24 to 32 weeks. MR imaging demonstrated morphological details of the anomalies. They were: alobar holoprosencephaly in 2, middle interhemispheric fusion in 1, alobar holoprosencephaly with Dandy-Walker malformations in 1, a Dandy-Walker variant in 1 and twin-twin transfusion syndrome with hypoxic-ischemic injury to the brain in 1.
Postmortem examinations confirmed the MR diagnoses, and these observations support us in improving our understanding of the pathogenesis of fetal CNS anomalies.
1998年至2000年期间,我们在超声检查后使用磁共振成像(MR)辅助58例复杂妊娠的产前咨询。
所有胎儿MR检查均采用1.5-T磁体,使用体部相控阵线圈和超快速成像技术,即半傅里叶单次激发快速自旋回波(HASTE)序列。发现12例胎儿有严重畸形,在这些病例中,要么引产,要么终止妊娠。其中6例中枢神经系统异常的胎儿在未能存活后进行了尸检,这些构成了本研究调查的患者样本。这6例胎儿的孕周为24至32周。MR成像显示了畸形的形态学细节。它们分别是:2例无脑叶全前脑畸形、1例大脑半球间融合、1例无脑叶全前脑畸形合并Dandy-Walker畸形、1例Dandy-Walker变异型和1例双胎输血综合征伴脑缺氧缺血性损伤。
尸检证实了MR诊断,这些观察结果有助于我们更好地理解胎儿中枢神经系统异常的发病机制。