Wenning G K, Quinn N, Magalhăes M, Mathias C, Daniel S E
University Department of Clinical Neurology, Institute of Neurology, London, England.
Mov Disord. 1994 Mar;9(2):161-6. doi: 10.1002/mds.870090206.
We describe the pathological findings in two patients who developed atypical parkinsonism and autonomic failure, leading to a diagnosis of multiple system atrophy (MSA). Postmortem examination of the brain showed cell loss restricted to substantia nigra and locus coeruleus. However, glial cytoplasmic inclusions (GCIs) were present in both cases. We propose that GCIs are highly suggestive of a pathological diagnosis of MSA in the absence of detectable cell loss outside pigmented brain stem nuclei and that brains from cases of atypical parkinsonism should routinely be examined for their presence.
我们描述了两名出现非典型帕金森症和自主神经功能衰竭并最终诊断为多系统萎缩(MSA)的患者的病理检查结果。对大脑进行的尸检显示,细胞丢失仅限于黑质和蓝斑。然而,这两个病例中均存在神经胶质细胞质包涵体(GCI)。我们提出,在脑桥色素核以外未检测到细胞丢失的情况下,GCI高度提示MSA的病理诊断,并且对于非典型帕金森症病例的大脑应常规检查是否存在GCI。