Raghavan R, Khin-Nu C, Brown A, Irving D, Ince P G, Day K, Tyrer S P, Perry R H
Department of Neuropathology, Newcastle General Hospital, Newcastle-upon-Tyne, United Kingdom.
Can J Neurol Sci. 1993 Feb;20(1):48-51. doi: 10.1017/s0317167100047405.
The presence of cortical senile plaques and neurofibrillary tangles sufficient to warrant a neuropathological diagnosis of Alzheimer's disease is well established in middle-aged individuals with Trisomy 21 (Down's syndrome). In contrast a relationship between Down's syndrome and Lewy bodies, one of the major neuropathological features of Parkinson's disease, has not been previously reported. In a clinico-neuropathological survey of 23 cases of Down's Syndrome, two patients, aged 50 and 56 years respectively, were found to have Lewy body formation in the substantia nigra in addition to cortical Alzheimer-type pathology. Neither case showed significant substantia nigra neuron loss although locus coeruleus loss was present in both. Since substantia nigra Lewy bodies are a characteristic neurohistological feature of idiopathic Parkinson's disease, their occurrence in cases of Down's syndrome with evidence of Alzheimer-type pathology supports an aetiopathological connection between Parkinson's disease, Alzheimer's disease, and Down's syndrome; and suggests that common pathogenic mechanisms may underlie aspects of neuronal degeneration in these three disorders, some of which may relate to aberrant chromosome 21 expression.
在患有21三体综合征(唐氏综合征)的中年个体中,足以确诊为阿尔茨海默病的皮质老年斑和神经原纤维缠结的存在已得到充分证实。相比之下,唐氏综合征与路易小体(帕金森病的主要神经病理学特征之一)之间的关系此前尚未见报道。在一项对23例唐氏综合征患者的临床神经病理学调查中,发现两名分别为50岁和56岁的患者,除了皮质型阿尔茨海默病病理改变外,黑质中还出现了路易小体形成。尽管两例患者的蓝斑均有丢失,但均未出现明显的黑质神经元丢失。由于黑质路易小体是特发性帕金森病的特征性神经组织学特征,它们在伴有阿尔茨海默病病理证据的唐氏综合征病例中的出现支持了帕金森病、阿尔茨海默病和唐氏综合征之间的病因病理联系;并表明这三种疾病中神经元变性的某些方面可能存在共同的致病机制,其中一些可能与21号染色体的异常表达有关。