Shimo Yasuji, Sato Kennichi, Iwamoto Hiroyuki, Motoi Yumiko, Mori Hideo, Urabe Takao, Mizuno Yoshikuni
Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, Japan.
No To Shinkei. 2005 Nov;57(11):1011-9.
We report a patient who developed personality change, dementia and parkinsonism. The patient was a Japanese woman who died at age 76. She developed memory problems at age 63. At age 66, she started showing personality changes, and began having short-step gait and mask-like face. On admission to our hospital at age 68, neurological examination showed mild memory deficit and postural instability. Six months after discharge, she developed delusion, rigidity, tremor, and gait disturbance. Her condition relentlessly progressed and she became bedridden at age 71. CT scan revealed marked atrophy of the frontotemporal lobes with enlargement of the lateral and third ventricles. The patient died at the age of 76 years. The patient was discussed in a neurological CPC, and a chief discussant arrived at the conclusion that the patient had frontotemporal dementia. Some participants thought that she had Pick disease or diffuse Lewy body disease. Severe atrophy of the frontal lobe and anterior part of the brain was seen at autopsy. Neuropathological examination showed severe neuronal loss with gliosis in the substantia nigra, pallidum, thalamus, and hippocampus. Moderate loss of neurons with gliosis was seen in the frontal and anterior temporal cortex. Argyrophilic and tau-positive neuronal inclusions which showed various shapes including Pick body-like inclusions and globose type of neurofibrillary tangles, were seen in the cerebral cortex and caudate. Argyrophilic and tau-positive astrocytes were also observed in the cerebral cortex. The pathological diagnosis was an unusual form of frontotemporal lobar degeneration with various tau-positive inclusions.
我们报告了一名出现人格改变、痴呆和帕金森综合征的患者。该患者为一名76岁去世的日本女性。她63岁时出现记忆问题。66岁时开始出现人格改变,并开始有短步幅步态和面具脸。68岁入院时,神经学检查显示轻度记忆缺陷和姿势不稳。出院6个月后,她出现妄想、强直、震颤和步态障碍。她的病情持续进展,71岁时卧床不起。CT扫描显示额颞叶明显萎缩,侧脑室和第三脑室扩大。患者76岁去世。该病例在一次神经科的临床病理讨论会(CPC)上进行了讨论,一位主要讨论者得出结论,该患者患有额颞叶痴呆。一些参与者认为她患有匹克病或弥漫性路易体病。尸检时可见额叶和脑前部严重萎缩。神经病理学检查显示黑质、苍白球、丘脑和海马体有严重神经元丢失伴胶质增生。额叶和颞叶前部皮质可见中度神经元丢失伴胶质增生。在大脑皮质和尾状核中可见嗜银性和tau阳性神经元包涵体,其形状各异,包括匹克小体样包涵体和球状神经原纤维缠结。在大脑皮质中也观察到嗜银性和tau阳性星形胶质细胞。病理诊断为一种伴有各种tau阳性包涵体的不寻常形式的额颞叶变性。