Sakai T, Miyamura M, Kuzuhara S
Department of Neurology, Ise Municipal Hospital.
Rinsho Shinkeigaku. 1992 Aug;32(8):859-63.
We report palilalia and acquired stuttering in a 60-year-old Japanese male with Parkinson's disease. At the age of 54, he presented with resting tremor in the hand and foot on the left, and gradual slowness in voluntary movements. Two years later, resting tremor involved the right foot, and an expressionless face and frozen gait occurred. A diagnosis of Parkinson's disease was made and treatment with L-dopa and carbidopa resulted in conspicuous improvement. At the age of 57, he developed compulsive repetitions of syllables, words and phrases, and sentences infrequently when he spoke. They have been persisting for four years. Repetitions increased in spontaneous speech while they decreased in oral reading and repetition of sentences. These repetitions in speech were symptomatologically diagnosed as palilalia and acquired stuttering. Brain CT showed slight brain atrophy, and brain MRI disclosed a few lesions indicating lacunae in the left substantia nigra, left putamen, and right internal capsule. SPECT showed a slight decrease in blood flow in the frontal lobes and basal ganglia bilaterally. Full IQ on WAIS was 105, and neither agnosia nor apraxia was detected. Palilalia and acquired stuttering, though the pathomechanism has not been clarified, have been reported to occur usually secondary to cerebral vascucular lesions and very rarely in Parkinson's disease. In the present case, they may have been produced by the parkinsonian nigro-striatal lesions. Alternatively, they may have been induced by the small vascular lesions demonstrated by MRI.
我们报告了一名60岁患帕金森病的日本男性出现复述言语和后天性口吃的病例。54岁时,他出现左手和左脚静止性震颤,以及随意运动逐渐迟缓。两年后,右脚出现静止性震颤,并出现面无表情和冻结步态。诊断为帕金森病,左旋多巴和卡比多巴治疗后有明显改善。57岁时,他说话时出现音节、单词、短语和句子的强迫性重复,不过句子重复较少见。这些症状持续了四年。自发言语中的重复增多,而朗读和句子复述时的重复减少。这些言语重复在症状学上被诊断为复述言语和后天性口吃。脑部CT显示轻度脑萎缩,脑部MRI显示左侧黑质、左侧壳核和右侧内囊有一些提示腔隙的病灶。单光子发射计算机断层扫描显示双侧额叶和基底神经节血流略有减少。韦氏成人智力量表测得的全量表智商为105,未检测到失认症和失用症。复述言语和后天性口吃,虽然发病机制尚未阐明,但据报道通常继发于脑血管病变,在帕金森病中非常罕见。在本病例中,它们可能是由帕金森病的黑质纹状体病变引起的。或者,它们可能是由MRI显示的小血管病变诱发的。