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两名患有门体分流且血锰升高的幼儿在T1加权图像上出现高强度基底神经节病变。

High-intensity basal ganglia lesions on T1-weighted images in two toddlers with elevated blood manganese with portosystemic shunts.

作者信息

Ihara K, Hijii T, Kuromaru R, Ariyoshi M, Kira R, Fukushige J, Hara T

机构信息

Department of Pediatrics, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Neuroradiology. 1999 Mar;41(3):195-8. doi: 10.1007/s002340050733.

DOI:10.1007/s002340050733
PMID:10206166
Abstract

We report two toddlers with portosystemic shunts who had symmetrical high-signal globus pallidus lesions on T1- but not T2-weighted MRI, and measurement of whole blood manganese at 2 years of age. These cases suggest that portosystemic shunts can cause elevation of blood manganese and result in manganese accumulation in the globus pallidus, causing high signal on T1-weighted images even in asymptomatic toddlers.

摘要

我们报告了两名患有门体分流的幼儿,他们在T1加权磁共振成像(MRI)上有对称性高信号的苍白球病变,但在T2加权MRI上没有,并且在2岁时测量了全血锰含量。这些病例表明,门体分流可导致血锰升高,并导致锰在苍白球中蓄积,即使在无症状的幼儿中也会在T1加权图像上产生高信号。

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