Kito Yumiko, Kazui Hiroaki, Yoshida Tetsuhiko, Kubo Yoshihiko, Takaya Masahiko, Tokunaga Hiromasa, Takeda Masatoshi
Psychiatry, Department of Integrated Medicine, Division of Internal Medicine, Osaka University Graduate School of Medicine, Suita-shi, Osaka, Japan.
Brain Nerve. 2010 Jun;62(6):625-30.
We report the rare case of a 59-year-old man with motor neuron disease and semantic dementia (SD-MND); SD-MND was in a very early stage, and its clinical progression, especially with regard to language impairment, and abnormalities on neuroimages were evaluated for 3 years. The patient complained only of difficulties in recalling names of acquaintances and in writing kanji characters. After 1 year, he experienced difficulty in describing common objects. He developed two-way anomia only in some words, which varied from day to day. His anomia was not category-specific and was noted even with respect to words that describe color. In addition to experiencing difficulty in writing kanji characters, he experienced difficulty in writing kana characters. Muscle atrophy was observed, and he experienced weakness in his limbs, especially in the right upper limb; however, bulbar symptoms were not observed. At this point, he fulfilled the diagnostic criteria for MND. In the next year, semantic memory impairment became apparent, and he was subsequently diagnosed with SD. Deterioration in his ability to name objects in all categories, except body parts, was noted. Further, the ability of writing both kana and kanji characters was increasingly impaired. He developed bulbar symptoms and experienced increased muscle weakness. The characteristics of this patient differed from those of SD patients without MND with regard to the difficulty in writing kana characters and naming colors even though the SD-MND was in the early stage. Further, the pattern of brain hypoperfusion was different from that observed for SD patients without MND. In the case of this patient, brain hypoperfusion was found not only in the left anterior temporal lobe but also in the frontal lobe. The characteristics of his language symptoms might be related to the specific pattern of brain hypoperfusion, which might be commonly observed in patients with dementia and MND.
我们报告了一例罕见的59岁男性患者,患有运动神经元病和语义性痴呆(SD-MND);SD-MND处于非常早期阶段,对其临床进展,尤其是语言障碍方面,以及神经影像异常情况进行了3年的评估。患者仅主诉在回忆熟人名字和书写汉字方面存在困难。1年后,他在描述常见物体时出现困难。他仅在某些单词上出现双向命名障碍,且每天有所不同。他的命名障碍并非特定类别性的,甚至在描述颜色的单词方面也有体现。除了书写汉字有困难外,他书写假名也有困难。观察到肌肉萎缩,且他四肢出现无力,尤其是右上肢;然而,未观察到延髓症状。此时,他符合运动神经元病的诊断标准。在接下来的一年里,语义记忆障碍变得明显,随后他被诊断为SD。注意到除身体部位外,他在所有类别物体命名能力方面均有恶化。此外,假名和汉字的书写能力越来越受损。他出现了延髓症状且肌肉无力加重。尽管该SD-MND处于早期阶段,但该患者在书写假名和命名颜色方面存在困难,这一点与无运动神经元病的SD患者不同。此外,脑灌注不足的模式与无运动神经元病的SD患者所观察到的不同。在该患者中,不仅在左侧颞前叶发现脑灌注不足,在额叶也有发现。他语言症状的特点可能与脑灌注不足的特定模式有关,这种模式可能在痴呆和运动神经元病患者中常见。