Iwasaki Yasushi, Mori Keiko, Ito Masumi, Tatsumi Shinsui, Mimuro Maya, Yoshida Mari
Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute.
Psychogeriatrics. 2013 Dec;13(4):260-4. doi: 10.1111/psyg.12030.
We present an autopsied case of a senile Japanese woman with sporadic frontotemporal lobar degeneration (FTLD) presenting as frontotemporal dementia. Disease onset was at the age of 70 and presented as a behaviour disorder, particularly involving wasteful habits. The patient had repeated incidents of making expensive purchases and then had difficulty making payments. Following these symptoms, she showed other changes of character such as lethargy and apathy. She gradually showed signs of parkinsonism including rigidity and bradykinesia, and in the terminal stage, an akinetic mutism state with quadriplegia in flexion was observed. Head magnetic resonance imaging revealed severe frontotemporal lobe atrophy with severe lateral ventricular dilatation and frontal white matter degeneration. At autopsy, the brain weighed 930 g and the frontotemporal cerebral cortex showed neuron loss with gliosis, tissue rarefaction and spongiform change, particularly in the superficial layers. Pathologic degeneration was more severe in the anterior portion of the frontal lobe with extensive white matter degeneration. Immunostaining for phosphorylated TAR-DNA binding protein 43 (TDP-43) revealed numerous neuronal cytoplasmic inclusions and extensive short dystrophic neuritis, particularly in the frontotemporal cortex. Many TDP-43-positive cytoplasmic inclusions were also observed in the dentate gyrus of the hippocampus. The patient was pathologically diagnosed with FTLD with TDP-43-positive inclusions (FTLD-TDP) without motor neuron disease. The immunohistochemical findings corresponded to type A of the FTLD-TDP pathology classification system.
我们报告一例老年日本女性尸检病例,该患者患有散发性额颞叶变性(FTLD),表现为额颞叶痴呆。发病年龄为70岁,以行为障碍为首发症状,尤其表现为挥霍习惯。患者反复出现购买昂贵物品后难以付款的情况。出现这些症状后,她还表现出其他性格变化,如嗜睡和冷漠。她逐渐出现帕金森综合征的体征,包括僵硬和运动迟缓,在疾病终末期,观察到一种屈曲性四肢瘫的运动不能性缄默状态。头部磁共振成像显示严重的额颞叶萎缩,伴有严重的侧脑室扩张和额叶白质变性。尸检时,大脑重量为930克,额颞叶皮质显示神经元丢失伴胶质细胞增生、组织稀疏和海绵状改变,尤其是在表层。额叶前部的病理变性更严重,伴有广泛的白质变性。磷酸化TAR-DNA结合蛋白43(TDP-43)免疫染色显示大量神经元胞质内包涵体和广泛的短营养不良性神经炎,尤其是在额颞叶皮质。在海马齿状回也观察到许多TDP-43阳性胞质内包涵体。该患者经病理诊断为伴有TDP-43阳性包涵体的FTLD(FTLD-TDP),无运动神经元病。免疫组化结果符合FTLD-TDP病理分类系统的A型。