Victoroff J, Ross G W, Benson D F, Verity M A, Vinters H V
Department of Neurology, UCLA School of Medicine.
Arch Neurol. 1994 Mar;51(3):269-74. doi: 10.1001/archneur.1994.00540150063018.
A subgroup of patients with progressive dementia has been reported with a marked predominance of symptoms attributed to the dysfunction of the posterior parieto-occipital cortex. These cases have been referred to as posterior cortical atrophy. The objective of this study was to determine whether posterior cortical atrophy is associated with distinct, uniform neuropathologic findings.
Three individuals with progressive dementia that began with higher visual dysfunction (posterior cortical atrophy) were followed up to definitive neuropathologic diagnosis.
Three separate neuropathologic entities were discovered: subcortical gliosis, Alzheimer's disease, and Creutzfeldt-Jakob disease.
Posterior cortical atrophy is a clinically homogeneous but pathologically heterogeneous syndrome.
据报道,一小部分进行性痴呆患者以明显归因于顶枕叶后部皮质功能障碍的症状为主。这些病例被称为后部皮质萎缩。本研究的目的是确定后部皮质萎缩是否与独特、一致的神经病理学发现相关。
对三名以高级视觉功能障碍起病的进行性痴呆患者(后部皮质萎缩)进行随访,直至明确神经病理学诊断。
发现了三种不同的神经病理学实体:皮质下胶质增生、阿尔茨海默病和克雅氏病。
后部皮质萎缩是一种临床同质但病理异质的综合征。