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基底神经节和小脑髓鞘形成不良伴萎缩:随访与病理

Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.

作者信息

van der Knaap M S, Linnankivi T, Paetau A, Feigenbaum A, Wakusawa K, Haginoya K, Köhler W, Henneke M, Dinopoulos A, Grattan-Smith P, Brockmann K, Schiffmann R, Blaser S

机构信息

Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands.

出版信息

Neurology. 2007 Jul 10;69(2):166-71. doi: 10.1212/01.wnl.0000265592.74483.a6.

Abstract

BACKGROUND AND OBJECTIVE

Hypomyelination with atrophy of the basal ganglia and cerebellum is a recently defined disorder. Only a few patients have been described. We report on 11 additional patients and new MRI findings and provide histopathologic confirmation of the MRI interpretation.

METHODS

We reviewed the patients' clinical history and present findings. We scored the MRI abnormalities. The histopathology of one patient was re-examined.

RESULTS

The patients' early psychomotor development was normal or delayed, followed by increasing extrapyramidal movement abnormalities, ataxia, and spasticity. Mental capacities were variably affected. MRI showed hypomyelination with, on follow-up, evidence of further myelin loss and variable white matter atrophy. The putamen was small or, more often, absent; the head of the caudate nucleus was decreased in size. In contrast, the thalamus and globus pallidus remained normal. Cerebellar atrophy was invariably present. Histopathology confirmed the myelin deficiency, probably related to both lack of deposition and low-grade further loss. The degeneration of putamen was subtotal. The cerebellar cortex was affected, particularly the granular layer.

CONCLUSION

Hypomyelination with atrophy of the basal ganglia and cerebellum is a syndrome diagnosed by distinctive MRI findings. Histopathology confirms hypomyelination, low-grade further myelin loss, subtotal degeneration of the putamen, and cerebellar cortical atrophy. All known patients are sporadic, and the mode of inheritance is unclear.

摘要

背景与目的

基底节和小脑髓鞘形成不良伴萎缩是一种最近才被定义的疾病。仅有少数患者被报道过。我们报告另外11例患者及新的MRI表现,并提供MRI解读的组织病理学证实。

方法

我们回顾了患者的临床病史及当前检查结果。对MRI异常进行评分。对1例患者的组织病理学进行了重新检查。

结果

患者早期精神运动发育正常或延迟,随后锥体外系运动异常、共济失调和痉挛加重。智力水平受到不同程度的影响。MRI显示髓鞘形成不良,随访时可见进一步的髓鞘丢失及不同程度的白质萎缩。壳核小或常常缺如;尾状核头部体积减小。相比之下,丘脑和苍白球保持正常。小脑萎缩始终存在。组织病理学证实髓鞘缺乏,可能与髓鞘沉积不足和轻度进一步丢失有关。壳核呈部分性变性。小脑皮质受累,尤其是颗粒层。

结论

基底节和小脑髓鞘形成不良伴萎缩是一种通过独特的MRI表现诊断的综合征。组织病理学证实髓鞘形成不良、轻度进一步髓鞘丢失、壳核部分性变性及小脑皮质萎缩。所有已知患者均为散发性,遗传方式尚不清楚。

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