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1型戊二酸血症:神经影像学特征与临床相关性

Glutaric aciduria type 1: neuroimaging features with clinical correlation.

作者信息

Mohammad Shaimaa Abdelsattar, Abdelkhalek Heba Salah, Ahmed Khaled A, Zaki Osama K

机构信息

Department of Radiodiagnosis, Faculty of Medicine, Ain-Shams University, 9 Ain-Shams university staff buildings, Lotfi Elsayed St., Cairo, Egypt, 11657.

Medical Genetics Unit, Pediatric Department, Faculty of Medicine, Ain-Shams University, Cairo, Egypt.

出版信息

Pediatr Radiol. 2015 Oct;45(11):1696-705. doi: 10.1007/s00247-015-3395-8. Epub 2015 Jun 26.

Abstract

BACKGROUND

Glutaric aciduria type 1 is a rare neurometabolic disease with high morbidity.

OBJECTIVE

To describe the MR imaging abnormalities in glutaric aciduria type 1 and to identify any association between the clinical and imaging features.

MATERIALS AND METHODS

MRI scans of 29 children (mean age: 16.9 months) with confirmed diagnosis of glutaric aciduria type 1 were retrospectively reviewed. Gray matter and white matter scores were calculated based on a previously published pattern-recognition approach of assessing leukoencephalopathies. Hippocampal formation and opercular topography were assessed in relation to the known embryological basis. MRI scores were correlated with morbidity score.

RESULTS

The most consistent MRI abnormality was widened operculum with dilatation of the subarachnoid spaces surrounding underdeveloped frontotemporal lobes. Incomplete hippocampal inversion was also seen. The globus pallidus was the most frequently involved gray matter structure (86%). In addition to the central tegmental tract, white matter abnormalities preferentially involved the central and periventricular regions. The morbidity score correlated with the gray matter abnormality score (P = 0.004). Patients with dystonia had higher gray matter and morbidity scores.

CONCLUSION

Morbidity is significantly correlated with abnormality of gray matter, rather than white matter, whether secondary to acute encephalopathic crisis or insidious onset disease.

摘要

背景

1型戊二酸尿症是一种罕见的神经代谢疾病,发病率较高。

目的

描述1型戊二酸尿症的磁共振成像异常,并确定临床特征与影像特征之间的任何关联。

材料与方法

回顾性分析29例确诊为1型戊二酸尿症的儿童(平均年龄:16.9个月)的MRI扫描结果。基于先前发表的评估白质脑病的模式识别方法计算灰质和白质评分。根据已知的胚胎学基础评估海马结构和脑岛形态。MRI评分与发病率评分相关。

结果

最一致的MRI异常是脑岛增宽,伴额颞叶发育不全周围蛛网膜下腔扩张。还可见海马反转不完全。苍白球是最常受累的灰质结构(86%)。除中央被盖束外,白质异常主要累及中央和脑室周围区域。发病率评分与灰质异常评分相关(P = 0.004)。肌张力障碍患者的灰质和发病率评分较高。

结论

无论是继发于急性脑病危象还是隐匿性发病疾病,发病率均与灰质异常显著相关,而非白质异常。

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