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经典型和变异型共济失调毛细血管扩张症的神经病理学。

Neuropathology in classical and variant ataxia-telangiectasia.

机构信息

Department of Pediatric Neurology, Donders Institute for Brain, Cognition and Behaviour Pathology, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

Neuropathology. 2012 Jun;32(3):234-44. doi: 10.1111/j.1440-1789.2011.01263.x. Epub 2011 Oct 24.

Abstract

Ataxia-telangiectasia (A-T) is classically characterized by progressive neurodegeneration, oculocutaneous telangiectasia, immunodeficiency and elevated α-fetoprotein levels. Some patients, classified as variant A-T, exhibit a milder clinical course. In the latter patients extrapyramidal symptoms, instead of cerebellar ataxia, tend to be the dominating feature and other classical disease hallmarks, like telangiectasia, appear later or even may be absent. Some patients with variant disease have clinically pronounced anterior horn cell degeneration. Neuropathological studies of genetically proven A-T patients are lacking. The aims of our study were to describe the neuropathology of three A-T patients; in two of them the diagnosis was genetically confirmed. The neuropathological findings were compared with those of all known published autopsy findings in A-T patients up to now. Two classical A-T patients aged 19 and 22 and a 33-year-old patient with variant disease were autopsied. In line with previous reports, our patients had severe cerebellar atrophy, less pronounced degeneration of the dentate nucleus and inferior olive, degeneration of the posterior columns and neurogenic muscular atrophy. In addition, all three had anterior horn cell degeneration, which was most prominent at the lumbar level. Compared to the literature, the degenerative changes in the brain stem of the variant A-T patient were somewhat less than anticipated for his age. Degenerative changes in the cerebellum and spinal cord were comparable with those in the literature. Progeric changes were lacking. In conclusion, compared to classical A-T, the variant A-T patient showed essentially the same, only slightly milder neuropathological abnormalities, except for anterior horn degeneration.

摘要

共济失调毛细血管扩张症(A-T)的特征为进行性神经退行性变、眼皮肤毛细血管扩张症、免疫缺陷和甲胎蛋白水平升高。一些患者,归类为变异型 A-T,表现为更轻微的临床病程。在后者患者中,锥体外系症状而非小脑共济失调倾向于成为主要特征,而其他经典疾病标志物,如毛细血管扩张症,出现较晚或甚至可能不存在。一些变异型疾病患者具有明显的临床前角细胞变性。缺乏对遗传证实的 A-T 患者的神经病理学研究。我们的研究目的是描述 3 名 A-T 患者的神经病理学;其中 2 名患者的诊断得到了基因证实。将神经病理学发现与迄今为止所有已知的 A-T 患者尸检发现进行了比较。对 2 名年龄分别为 19 岁和 22 岁的经典 A-T 患者和 1 名 33 岁的变异型疾病患者进行了尸检。与先前的报道一致,我们的患者有严重的小脑萎缩,齿状核和下橄榄核的退行性变不那么明显,后柱和神经源性肌肉萎缩的退行性变。此外,所有患者均有前角细胞变性,在腰椎水平最为突出。与文献相比,变异型 A-T 患者脑干的退行性改变比预期的年龄稍轻。小脑和脊髓的退行性改变与文献相似。缺乏进行性变化。总之,与经典 A-T 相比,变异型 A-T 患者除了前角细胞变性外,表现出基本相同的、仅略微轻微的神经病理学异常。

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