Suppr超能文献

在诊断胎儿骶骨发育不全时考虑脊髓圆锥。

Think of the Conus Medullaris at the Time of Diagnosis of Fetal Sacral Agenesis.

作者信息

Mottet Nicolas, Martinovic Jelena, Baeza Claire, Guimiot Fabien, Bault Jean-Philippe, Aubry Marie Cécile, Riethmuller Didier, Zerah Michel, Cretolle Celia, Benachi Alexandra

机构信息

Department of Obstetrics, Gynecology and Reproductive Medicine, Hospital Antoine Béclère, AP-HP, Université Paris-Sud, Paris, France.

出版信息

Fetal Diagn Ther. 2017;42(2):137-143. doi: 10.1159/000451080. Epub 2016 Oct 29.

Abstract

BACKGROUND

There is no precise prenatal indicator to refine an accurate prognosis in case of sacral agenesis and to define the diagnostic approach and outcome criteria in case of fetal sacral agenesis using 3 characteristics of the conus medullaris (CM): its position, its appearance, and associated spinal abnormalities.

METHODS

Ten cases of prenatally diagnosed sacral agenesis were included between 1995 and 2014 after collating ultrasound findings and prenatal computed tomography data.

RESULTS

Two cases of total sacral agenesis and 8 of partial agenesis were included. There were 1 or more spinal abnormalities in 8/10 cases: 6 lipomas, 4 low-lying tethered cords, 2 diastematomyelias, and 1 syringomyelia. Three situations were distinguished: sacral agenesis with low-lying tethered cord, sacral agenesis with a truncated CM, and sacral agenesis with CM in place. If the sacral agenesis is isolated, a lipoma should be sought. Lipomas of the filum have a good prognosis, whereas lipomas of the CM cause neurological deficits in 1/3 of cases. When there is a low-lying tethered cord, a diastematomyelia or a syringomyelia may be associated. In truncated CM, there may be a severe form suggestive of caudal regression syndrome. Serious ultrasound signs are immobility of the lower limbs, talipes equinovarus, impaired bladder emptying, and dilatation of the upper urinary tract.

CONCLUSION

A precise description of the morphology of the CM, its position, and associated spinal malformations are important in defining the neurological, urinary, gastrointestinal, and motor functions prognosis in cases of fetal sacral agenesis.

摘要

背景

在骶骨发育不全的情况下,没有精确的产前指标来完善准确的预后评估,也无法利用脊髓圆锥(CM)的三个特征(其位置、外观和相关脊柱异常)来确定胎儿骶骨发育不全的诊断方法和预后标准。

方法

在整理超声检查结果和产前计算机断层扫描数据后,纳入了1995年至2014年间产前诊断为骶骨发育不全的10例病例。

结果

包括2例完全性骶骨发育不全和8例部分性发育不全。10例中有8例存在1种或多种脊柱异常:6例脂肪瘤、4例低位脊髓栓系、2例脊髓纵裂和1例脊髓空洞症。区分出三种情况:伴有低位脊髓栓系的骶骨发育不全、伴有截断性脊髓圆锥的骶骨发育不全和脊髓圆锥位置正常的骶骨发育不全。如果骶骨发育不全是孤立性的,应寻找脂肪瘤。终丝脂肪瘤预后良好,而脊髓圆锥脂肪瘤在1/3的病例中会导致神经功能缺损。当存在低位脊髓栓系时,可能伴有脊髓纵裂或脊髓空洞症。在截断性脊髓圆锥的情况下,可能存在提示尾椎退化综合征的严重形式。严重的超声征象包括下肢活动受限、马蹄内翻足、膀胱排空障碍和上尿路扩张。

结论

精确描述脊髓圆锥的形态、其位置以及相关脊柱畸形,对于确定胎儿骶骨发育不全病例的神经、泌尿、胃肠和运动功能预后至关重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验