Hatanpaa K J, Blass D M, Pletnikova O, Crain B J, Bigio E H, Hedreen J C, White C L, Troncoso J C
Department of Pathology, University of Texas Southwestern Medical School, Dallas 75390-9073, USA.
Neurology. 2004 Aug 10;63(3):538-42. doi: 10.1212/01.wnl.0000129543.46734.c0.
Hippocampal sclerosis dementia (HSD) is a disease of unknown etiology and pathogenesis. To determine whether HSD cases could be reclassified as variants of frontotemporal dementia (FTD), a heterogeneous group of disorders, 18 brain autopsy cases previously diagnosed as HSD were re-evaluated. In 11 cases, ubiquitinated neuronal inclusions, similar to those of motor neuron disease inclusion dementia (MNDID), were found. Brain levels of soluble and insoluble tau were normal. Most patients with pathologic findings of HSD may actually have the MNDID variant of FTD.
海马硬化性痴呆(HSD)是一种病因和发病机制不明的疾病。为了确定HSD病例是否可重新分类为额颞叶痴呆(FTD,一组异质性疾病)的变异型,对18例先前诊断为HSD的脑尸检病例进行了重新评估。在11例病例中,发现了与运动神经元病包涵体痴呆(MNDID)相似的泛素化神经元包涵体。可溶性和不溶性tau蛋白的脑内水平正常。大多数有HSD病理表现的患者实际上可能患有FTD的MNDID变异型。