Ota Satoru, Tsuchiya Kuniaki, Anno Midori, Akiyama Haruhiko
Department of Neurology, Tokyo Metropolitan Matsuzawa Hospital, 2-1-1 Kamikitazawa, Setagaya-ku, Tokyo 156-0057, Japan.
No To Shinkei. 2005 Mar;57(3):233-8.
We report an autopsy case of dementia lacking distinctive histology (DLDH) showing semantic dementia. At age 47, a Japanese man developed aspontaneity, followed by semantic dementia a few months after the onset. Thereafter he developed disinhibition and the language disturbance, which progressed transcortical sensory aphasia and terminally mixed transcortical aphasia. At age 48, about 10 months after the disease onset, neurological examination revealed frontal signs and hyperreflexia in the four extremities and 4 months later, the patient presented with mild rigidity in the right upper and lower extremities. At age 49, 1 year and 8 months after the onset of the disease, he could not walk by himself. At age 50, 2 years and 8 months after the onset, he died of pneumonia. The brain weighed 1350 g. Macroscopically, atrophy of the frontal lobes and temporal lobes, predominant in the left, was evident. The caudate nucleus was severely atrophic, in addition to the depigmentation of the substantia nigra. Neuronal loss and astrocytosis was obvious in the cerebral cortex, prominently in the frontotemporal lobes, amygdala, caudate nucleus, putamen, pallidum, thalamus, and substantia nigra. In the caudate nucleus, prominent neuronal loss with fibrillary gliosis was obvious. Senile plaques, neurofibrillary tangles, Pick bodies, astrocytic plaques, and tufted astrocytes were not found by Gallyas and tau staining. Ubiquitin-immunoreactive intracytoplasmic inclusions were not encountered in the hippocampal dentate gyrus and superficial layers in the frontotemporal cortex. On the basis of meticulous perusal of the literature, we believe that our case is the first autopsy case of DLDH reported in Japan.
我们报告一例缺乏特异性组织学改变的痴呆症(DLDH)尸检病例,该病例表现为语义性痴呆。一名47岁的日本男性出现自发性症状,发病数月后出现语义性痴呆。此后,他出现了脱抑制和语言障碍,并进展为经皮质感觉性失语,最终发展为混合性经皮质失语。48岁时,即疾病发作约10个月后,神经学检查发现额叶体征和四肢反射亢进,4个月后,患者右上肢和下肢出现轻度强直。49岁时,疾病发作1年零8个月后,他无法独立行走。50岁时,疾病发作2年零8个月后,他死于肺炎。脑重1350克。宏观上,额叶和颞叶萎缩明显,以左侧为主。除黑质色素脱失外,尾状核严重萎缩。大脑皮质神经元丢失和星形细胞增生明显,主要见于额颞叶、杏仁核、尾状核、壳核、苍白球、丘脑和黑质。在尾状核中,明显的神经元丢失伴纤维性胶质增生。通过Gallyas染色和tau染色未发现老年斑、神经原纤维缠结、Pick小体、星形细胞斑和簇状星形细胞。在海马齿状回和额颞叶皮质浅层未发现泛素免疫反应性胞浆内包涵体。在仔细查阅文献的基础上,我们认为我们的病例是日本报道的首例DLDH尸检病例。