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伴有钙化和囊肿的脑视网膜微血管病

Cerebroretinal microangiopathy with calcifications and cysts.

作者信息

Linnankivi T, Valanne L, Paetau A, Alafuzoff I, Hakumäki J M, Kivelä T, Lönnqvist T, Mäkitie O, Pääkkönen L, Vainionpää L, Vanninen R, Herva R, Pihko H

机构信息

Department of Pediatric Neurology, Hospital for Children and Adolescents, University of Helsinki, Stenbäckinkatu 11, FIN-00290 Helsinki, Finland.

出版信息

Neurology. 2006 Oct 24;67(8):1437-43. doi: 10.1212/01.wnl.0000236999.63933.b0. Epub 2006 Aug 30.

Abstract

BACKGROUND

Extensive cerebral calcifications and leukoencephalopathy have been reported in two rare disorders Coats plus and leukoencephalopathy with calcifications and cysts. In the latter, a progressive formation of parenchymal brain cysts is a special feature, whereas Coats plus is characterized by intrauterine growth retardation, bilateral retinal telangiectasias and exudations (Coats disease), sparse hair, and dysplastic nails without cyst formation.

METHODS

We identified 13 patients, including two pairs of siblings, with extensive cerebral calcifications and leukoencephalopathy. We reviewed clinical, ophthalmologic, radiologic and neuropathologic data of seven deceased patients and studied five patients prospectively.

RESULTS

Eleven patients were small for gestational age; the other symptoms emerged from infancy to adolescence. All patients had neurologic symptoms including seizures, spasticity, dystonia, ataxia, and cognitive decline. Progressive intracerebral calcifications involved deep gray nuclei, brainstem, cerebral and cerebellar white matter, and dentate nuclei and were accompanied by diffuse white matter signal changes and, in five patients, cerebral cysts. Eleven patients had retinal telangiectasias or angiomas. Additional features were skeletal and hematologic abnormalities, intestinal bleeding, and poor growth. Neuropathologic examination showed extensive calcinosis and abnormal small vessels with thickened, hyalinized wall and reduced lumen.

CONCLUSIONS

Our data suggest that Coats plus syndrome and leukoencephalopathy with calcifications and cysts belong to the same spectrum. The primary abnormality seems to be an obliterative cerebral angiopathy involving small vessels, leading to dystrophic calcifications via slow necrosis and finally to formation of cysts and secondary white matter abnormalities.

摘要

背景

在两种罕见疾病——科茨综合征(Coats plus)和伴有钙化及囊肿的白质脑病中,均有广泛脑钙化和白质脑病的报道。在后者中,脑实质囊肿的进行性形成是一个特殊特征,而科茨综合征的特征为宫内生长迟缓、双侧视网膜毛细血管扩张和渗出(科茨病)、头发稀疏及指甲发育异常,无囊肿形成。

方法

我们确定了13例患有广泛脑钙化和白质脑病的患者,包括两对兄弟姐妹。我们回顾了7例已故患者的临床、眼科、放射学和神经病理学数据,并对5例患者进行了前瞻性研究。

结果

11例患者出生时体重低于孕周;其他症状从婴儿期到青春期出现。所有患者均有神经症状,包括癫痫发作、痉挛、肌张力障碍、共济失调和认知功能下降。进行性脑内钙化累及深部灰质核团、脑干、大脑和小脑白质以及齿状核,并伴有弥漫性白质信号改变,5例患者有脑囊肿。11例患者有视网膜毛细血管扩张或血管瘤。其他特征包括骨骼和血液系统异常、肠道出血和生长发育不良。神经病理学检查显示广泛的钙质沉着和异常小血管,血管壁增厚、玻璃样变,管腔变窄。

结论

我们的数据表明,科茨综合征和伴有钙化及囊肿的白质脑病属于同一谱系。主要异常似乎是一种累及小血管的闭塞性脑血管病,通过缓慢坏死导致营养不良性钙化,最终形成囊肿和继发性白质异常。

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