Brown D F, Dababo M A, Bigio E H, Risser R C, Eagan K P, Hladik C L, White C L
Department of Pathology, University of Texas Southwestern Medical School, Dallas 75235-9072, USA.
J Neuropathol Exp Neurol. 1998 Jan;57(1):39-46. doi: 10.1097/00005072-199801000-00006.
We undertook this study to investigate the neuropathologic relationships among Alzheimer disease (AD), idiopathic Parkinson disease (PD), and the Lewy body variant of AD (AD/LBV). We retrieved 30 autopsy cases in which Lewy bodies (LB) had been identified in the substantia nigra (SN) in routine hematoxylin-eosin-stained sections. Twenty-two of the cases had a primary clinical diagnosis of dementia and neuropathologic changes of AD; 12 of these demented patients also had clinical parkinsonism. Eight cases had clinical and neuropathologic evidence of PD with minimal or no AD neuropathology, though 6 had clinical dementia. Controls consisted of 6 cases of AD without SN LB by hematoxylin-eosin, and 5 neurologically normal aged controls. Paraffin sections of SN, superior temporal gyrus, and cingulate gyrus from each case were immunostained with rabbit anti-ubiquitin antiserum, randomized, and analyzed individually by light microscopy, and the density of LB-like profiles in each section were graded. None of 5 nondemented aged controls showed any neocortical LB, even though 2 had significant numbers of incidental SN LB by ubiquitin immunostaining. Of 6 AD cases without SN LB by hematoxylin-eosin, 3 had rare SN LB on ubiquitin stain, 1 of which showed rare neocortical Lewy-like profiles. Seven of 8 PD cases showed neocortical LB, including the 6 with dementia. Twenty-one of 22 AD cases with SN LB showed ubiquitin-immunoreactive Lewy-like bodies in the neocortex that were statistically significantly greater in number than in either pure PD or pure AD cases. The frequent occurrence of LB in the neocortex in PD alone suggests that AD/LBV likely represents mixed AD/PD. However, AD neuropathology may favor or promote the formation of neocortical LB in patients who go on to develop mixed AD/PD pathology.
我们开展这项研究以调查阿尔茨海默病(AD)、特发性帕金森病(PD)以及AD路易体变异型(AD/LBV)之间的神经病理学关系。我们检索了30例尸检病例,这些病例在苏木精-伊红染色的常规切片中黑质(SN)存在路易小体(LB)。其中22例最初临床诊断为痴呆且有AD的神经病理学改变;这些痴呆患者中有12例也有临床帕金森综合征。8例有PD的临床和神经病理学证据且AD神经病理学改变轻微或无改变,不过其中6例有临床痴呆。对照组包括6例苏木精-伊红染色显示SN无LB的AD病例以及5例神经功能正常的老年对照。对每个病例的SN、颞上回和扣带回的石蜡切片用兔抗泛素抗血清进行免疫染色,随机排列,然后通过光学显微镜单独分析,对每个切片中路易小体样结构的密度进行分级。5例非痴呆老年对照中无一例显示新皮质有LB,尽管其中2例通过泛素免疫染色在SN有大量偶发性LB。在6例苏木精-伊红染色显示SN无LB的AD病例中,3例在泛素染色时SN有罕见的LB,其中1例显示新皮质有罕见的路易小体样结构。8例PD病例中有7例显示新皮质有LB,包括6例有痴呆的病例。22例SN有LB的AD病例中有21例新皮质显示泛素免疫反应性路易小体样结构,其数量在统计学上显著多于单纯PD或单纯AD病例。仅在PD中新皮质频繁出现LB提示AD/LBV可能代表AD/PD混合型。然而,AD神经病理学可能有利于或促进发展为AD/PD混合型病理的患者新皮质LB的形成。