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丘脑T2信号降低可能是溶酶体贮积病的一个迹象。

Decreased T2 signal in the thalami may be a sign of lysosomal storage disease.

作者信息

Autti Taina, Joensuu Raimo, Aberg Laura

机构信息

Helsinki Medical Imaging Center, Helsinki University Central Hospital, P.O. Box 340, 00029-HUS, Helsinki, Finland.

出版信息

Neuroradiology. 2007 Jul;49(7):571-8. doi: 10.1007/s00234-007-0220-6. Epub 2007 Mar 3.

Abstract

INTRODUCTION

Lysosomal disorders are rare and are caused by genetically transmitted lysosomal enzyme deficiencies. A decreased T2 signal in the thalamus has occasionally been reported.

AIMS

Because the finding of bilateral abnormal signal intensity of the thalamus on T2-weighted images has not been systematically reviewed, and its value as a diagnostic tool critically evaluated, we carried out a systematic review of the literature.

METHODS

Articles in English with 30 trios of keywords were collected from PubMed. Exclusion criteria were lack of conventional T2-weighted images in the protocol and not being a human study. Finally, 111 articles were included. The thalamus was considered affected only if mentioned in the text or in the figure legends.

RESULTS

Some 117 patients with various lysosomal diseases and five patients with ceruloplasmin deficiency were reported to have a bilateral decrease in T2 signal intensity. At least one article reported a bilateral decrease in signal intensity of the thalami on T2-weighted images in association with GM1 and GM2 gangliosidosis and with Krabbe's disease, aspartylglucosaminuria, mannosidosis, fucosidosis, and mucolipidosis IV. Furthermore, thalamic alteration was a consistent finding in several types of neuronal ceroid lipofuscinosis (NCL) including CLN1 (infantile NCL), CLN2 (classic late infantile NCL), CLN3 (juvenile NCL), CLN5 (Finnish variant late infantile NCL), and CLN7 (Turkish variant late infantile NCL).

CONCLUSION

A decrease in T2 signal intensity in the thalami seems to be a sign of lysosomal disease.

摘要

引言

溶酶体疾病较为罕见,由遗传传递的溶酶体酶缺乏引起。偶尔有报道称丘脑的T2信号降低。

目的

由于尚未对T2加权图像上丘脑双侧异常信号强度的发现进行系统综述,也未对其作为诊断工具的价值进行严格评估,因此我们对文献进行了系统综述。

方法

从PubMed收集了包含30组关键词的英文文章。排除标准为方案中缺乏常规T2加权图像以及非人体研究。最终纳入111篇文章。仅当文本或图注中提及丘脑时,才认为丘脑受到影响。

结果

据报道,约117例患有各种溶酶体疾病的患者和5例患有铜蓝蛋白缺乏症的患者丘脑T2信号强度双侧降低。至少有一篇文章报道,在T2加权图像上,丘脑信号强度双侧降低与GM1和GM2神经节苷脂沉积症、克拉伯病、天冬氨酰葡糖胺尿症、甘露糖苷贮积症、岩藻糖苷贮积症和黏脂贮积症IV相关。此外,在几种类型的神经元蜡样脂褐质沉积症(NCL)中,包括CLN1(婴儿型NCL)、CLN2(经典晚婴儿型NCL)、CLN3(青少年型NCL)、CLN5(芬兰变异型晚婴儿型NCL)和CLN7(土耳其变异型晚婴儿型NCL),丘脑改变是一个一致的发现。

结论

丘脑T2信号强度降低似乎是溶酶体疾病的一个征象。

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