Verity M A, Roitberg B, Kepes J J
Department of Pathology, UCLA Medical Center, 90024-1732.
J Neurol Neurosurg Psychiatry. 1990 Jun;53(6):492-5. doi: 10.1136/jnnp.53.6.492.
The clinicopathological findings are presented of two cases of mesolimbocortical dementia. Both cases were characterised by late onset slowly progressive personality changes and progressive intellectual deterioration without clinical Parkinsonism. Neuropathological findings revealed non-specific neuronal degeneration, Holzer and GFAP positive gliosis primarily affecting the limbic system, caudate, thalamus and substantia nigra. The pathological findings coincide with the distribution of the non-striatal dopaminergic pathways and suggest an intrinsic involvement of these pathways to account for the clinical and pathological manifestations.
本文呈现了两例中脑边缘叶皮质痴呆的临床病理研究结果。两例患者均表现为起病较晚、缓慢进展的人格改变以及进行性智力衰退,且无临床帕金森综合征表现。神经病理学检查发现非特异性神经元变性,霍尔泽(Holzer)和胶质纤维酸性蛋白(GFAP)阳性的胶质增生主要累及边缘系统、尾状核、丘脑和黑质。这些病理结果与非纹状体多巴胺能通路的分布一致,提示这些通路的内在受累可解释其临床和病理表现。