Jellinger K, Seitelberger F
Am J Med Genet Suppl. 1986;1:259-88. doi: 10.1002/ajmg.1320250528.
Autopsy studies in 8 girls with the Rett syndrome dying between 4 and 15 years showed: Diffuse cerebral atrophy/micrencephaly, with a decrease in brain weight by 13.8 to 33.8% of age-matched controls, apparently related to the duration of the disorder; Mild, but inconsistent diffuse cortical atrophy without developmental disorders apart from occasional microdysgenesis (three cases), but increased amounts of neuronal lipofuscin, and occasional mild astrocytic gliosis; Mild, but inconsistent spongy changes in cerebral and cerebellar white matter, optic nerve (two cases), and myelinated fascicles of the brainstem tegmentum, without signs of dys- or demyelination, and apparently different from the spongy myelinopathy common to aminoacidopathies; Most conspicuous was an underpigmentation of the substantia nigra which contained many fewer well-pigmented neurons for age (53-73%), and fewer pigmented granules per neuron, while the total number of nigral neurons and the triphasic substructure of neuromelanin were normal for age. No pathologic changes were seen in locus coeruleus, nucleus basalis of Meynert, and nucleus dorsalis raphe; Electron microscopy of autopsy material from an 11-year-old girl showed increased amounts of neuronal lipofuscin without signs of a storage disorder. Reactive and degenerating axons in the caudate nucleus were possibly related to the nigral changes, suggesting some dysfunction of the dopaminergic nigro-striatal system, while the synaptic organization of the neostriatum appeared unaffected. Peripheral nerve from a patient dying in advanced stage showed increased numbers of unmyelinated (regenerated?) axons, with almost no demyelination and few remyelinated axons, suggesting axonal degeneration rather than hypomyelination, but exogenous factors (malnutrition) cannot be excluded. The pathogenetic mechanisms of the morphologic brain lesions and their relations to clinical and neurochemical findings in Rett syndrome are unknown and deserve further intensive investigations.
对8名4至15岁死亡的雷特综合征女孩进行的尸检研究显示:弥漫性脑萎缩/小脑发育不全,脑重量比年龄匹配的对照组减少13.8%至33.8%,这显然与疾病持续时间有关;轻度但不一致的弥漫性皮质萎缩,除偶尔有微小发育异常(3例)外无发育障碍,但神经元脂褐素增多,偶尔有轻度星形胶质细胞增生;大脑和小脑白质、视神经(2例)以及脑干被盖部有髓神经束有轻度但不一致的海绵状改变,无脱髓鞘或髓鞘形成异常迹象,且明显不同于氨基酸代谢病常见的海绵状髓鞘病;最显著的是黑质色素沉着不足,与年龄相符的色素沉着良好的神经元数量减少(53 - 73%),每个神经元的色素颗粒减少,而黑质神经元总数和神经黑素的三相亚结构在年龄上是正常的。在蓝斑、梅纳特基底核和中缝背核未发现病理变化;对一名11岁女孩尸检材料的电子显微镜检查显示神经元脂褐素增多,无储存障碍迹象。尾状核中反应性和变性的轴突可能与黑质变化有关,提示多巴胺能黑质 - 纹状体系统存在某种功能障碍,而新纹状体的突触组织似乎未受影响。一名晚期死亡患者的周围神经显示无髓鞘(再生?)轴突数量增加,几乎无脱髓鞘,再髓鞘化轴突很少,提示轴突变性而非髓鞘形成不足,但不能排除外源性因素(营养不良)。雷特综合征中脑形态学病变的发病机制及其与临床和神经化学发现的关系尚不清楚,值得进一步深入研究。