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1型戊二酸血症的神经影像学表现

Neuroimaging findings in glutaric aciduria type 1.

作者信息

Twomey Eilish L, Naughten Eileen R, Donoghue Veronica B, Ryan Stephanie

机构信息

Department of Radiology, Children's University Hospital, Temple Street, Dublin 1, Ireland.

出版信息

Pediatr Radiol. 2003 Dec;33(12):823-30. doi: 10.1007/s00247-003-0956-z. Epub 2003 Oct 8.

DOI:10.1007/s00247-003-0956-z
PMID:14534757
Abstract

OBJECTIVE

To review the imaging features of glutaric aciduria type 1 (GA-1) in a group of 20 patients, the largest published series to date. To document the findings not previously reported and compare our findings with the imaging characteristics of GA-1 previously reported in the literature.

MATERIALS AND METHODS

For 14 patients the original scans were examined and in the remaining 6, where the imaging was unavailable, the radiology reports were consulted. Nine patients had serial cranial US examinations, 13 had 18 CT scans performed and 14 patients had 39 MRI scans.

RESULTS

Widening of the sylvian fissures and of the fluid spaces anterior to the temporal lobes was seen in 93% of cases. The mesencephalic cistern was also widened in 86%. Abnormal high-signal intensity on T2-weighted (T2-W) images was seen in the basal ganglia and periventricular white matter in 64% of children. Subdural collections were found in 3 patients, all of which resolved spontaneously. Four neonates followed with serial cranial US showed bilateral multiple caudothalamic cysts. Abnormal high signal on T2-W images was seen in the dentate nucleus, substantia nigra and the pontine medial lemniscus in 79, 43 and 64%, respectively.

CONCLUSIONS

Widening of the sylvian fissure, mesencephalic cistern and expansion of CSF spaces anterior to the temporal lobes are cardinal signs of GA-1. If combined with abnormalities of the basal ganglia and white matter, GA-1 should be strongly suspected.

摘要

目的

回顾20例戊二酸血症1型(GA-1)患者的影像特征,这是迄今为止发表的最大系列病例。记录此前未报道的发现,并将我们的发现与文献中先前报道的GA-1影像特征进行比较。

材料与方法

对14例患者的原始扫描影像进行检查,其余6例无法获取影像资料的患者则查阅其放射学报告。9例患者接受了系列头颅超声检查,13例进行了18次CT扫描,14例患者进行了39次MRI扫描。

结果

93%的病例可见外侧裂及颞叶前方液间隙增宽。86%的病例中脑导水管也增宽。64%的儿童在T2加权(T2-W)图像上基底节和脑室周围白质出现异常高信号强度。3例患者发现硬膜下积液,均自行消退。4例接受系列头颅超声检查的新生儿显示双侧多发丘脑尾状核囊肿。分别有79%、43%和64%的患者在T2-W图像上齿状核、黑质和脑桥内侧丘系出现异常高信号。

结论

外侧裂、中脑导水管增宽及颞叶前方脑脊液间隙扩大是GA-1的主要征象。若同时合并基底节和白质异常,则应高度怀疑GA-1。

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