A comparative MR and pathological study on fetal CNS disorders

被引:27
作者
Guo, WY
Chang, CY
Ho, DMT
Wong, TT
Sheu, MH
Cheng, HC
Chen, SJ
Hung, JH
机构
[1] Vet Gen Hosp, Dept Radiol, Taipei 11217, Taiwan
[2] Vet Gen Hosp, Dept Pathol, Taipei 11217, Taiwan
[3] Vet Gen Hosp, Neurol Inst, Taipei 11217, Taiwan
[4] Vet Gen Hosp, Dept Pediat, Taipei 11217, Taiwan
[5] Vet Gen Hosp, Dept Obstet & Gynecol, Taipei 11217, Taiwan
[6] Natl Yang Ming Univ, Sch Med, Dept Radiol, Taipei 11217, Taiwan
[7] Natl Yang Ming Univ, Sch Med, Dept Pathol, Taipei 11217, Taiwan
[8] Natl Yang Ming Univ, Sch Med, Neurol Inst, Taipei 11217, Taiwan
[9] Natl Yang Ming Univ, Sch Med, Dept Pediat, Taipei 11217, Taiwan
[10] Natl Yang Ming Univ, Sch Med, Dept Obstet & Gynecol, Taipei 11217, Taiwan
关键词
fetal MR; postmortem examination; comparative study; congenital anomalies; central nervous system; prenatal counseling;
D O I
10.1007/s003810100471
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object: We used MR after sonography to help us in prenatal counseling in 58 complicated pregnancies from 1998 to 2000. Methods: 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 sin-le-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. Conclusions: Postmortem examinations confirmed the MR diagnoses, and these observations support us in improving our understanding of the pathogenesis of fetal CNS anomalies.
引用
收藏
页码:512 / 518
页数:7
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