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扩散加权成像和表观扩散系数(ADC)图在一名患有自身免疫性桥本甲状腺炎的成年异染性脑白质营养不良患者的皮质下白质中检测到正在进行的脱髓鞘病变。

Diffusion and ADC-map images detect ongoing demyelination on subcortical white matter in an adult metachromatic leukodystrophy patient with autoimmune Hashimoto thyroiditis.

作者信息

Miura Akiko, Kumabe Yuri, Kimura En, Yamashita Satoshi, Ueda Akihiko, Hirano Teruyuki, Uchino Makoto

机构信息

Department of Neurology, Kumamoto University Hospital, Kumamoto, Japan.

出版信息

BMJ Case Rep. 2010 Dec 1;2010:bcr0120102631. doi: 10.1136/bcr.01.2010.2631.

Abstract

Adult-onset metachromatic leukodystrophy (MLD) often shows schizophrenia- or encephalopathy-like symptoms at an early stage, such as behavioural abnormalities, cognitive impairment, mood disorders and hallucinations. The authors report the case of an adult woman with MLD who had been given antipsychotic medication for schizophrenia. In the differential diagnosis, screening of auto-antibodies was important for ruling out other encephalopathies as she had a euthyroid Hashimoto thyroiditis. Diagnosis was based the results of MRI, nerve conduction velocity, sensory evoked potential, motor evoked potential, lysosomal enzyme activity and gene analysis studies. Brain MRI showed diffuse demyelination spreading from the deep white matter to subcortical area as high signals at the edges of these lesions in diffusion and apparent diffusion coefficient-map images with the U-fibres conserved. The authors diagnosed adult-onset MLD coexisting with euthyroid autoimmune Hashimoto thyroiditis.

摘要

成人起病的异染性脑白质营养不良(MLD)在早期常表现出精神分裂症样或脑病样症状,如行为异常、认知障碍、情绪障碍和幻觉。作者报告了一例患有MLD的成年女性病例,该患者曾因精神分裂症接受抗精神病药物治疗。在鉴别诊断中,由于她患有甲状腺功能正常的桥本甲状腺炎,自身抗体筛查对于排除其他脑病很重要。诊断基于磁共振成像(MRI)、神经传导速度、感觉诱发电位、运动诱发电位、溶酶体酶活性和基因分析研究的结果。脑部MRI显示弥漫性脱髓鞘,从深部白质扩散至皮质下区域,在扩散加权成像和表观扩散系数图图像中,这些病变边缘呈高信号,U形纤维保留。作者诊断该患者为成人起病的MLD合并甲状腺功能正常的自身免疫性桥本甲状腺炎。

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本文引用的文献

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Motor and psycho-cognitive clinical types in adult metachromatic leukodystrophy: genotype/phenotype relationships?
J Physiol Paris. 2002 Apr-Jun;96(3-4):301-6. doi: 10.1016/s0928-4257(02)00019-0.
10
Hashimoto encephalopathy: etiologic considerations.
Pediatr Neurol. 1994 Nov;11(4):328-31. doi: 10.1016/0887-8994(94)90011-6.

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