Beatty W W, Scott J G, Wilson D A, Prince J R, Williamson D J
Department of Psychiatry and Behavioral Sciences, University of Oklahoma Health Sciences Center, Oklahoma City 73190, USA.
J Geriatr Psychiatry Neurol. 1995 Apr;8(2):132-6. doi: 10.1177/089198879500800212.
Anterograde and retrograde amnesia in a patient with probable corticobasal degeneration (pCBD) and dementia were studied in a university medical center setting. The patient with pCBD and four comparison patients of comparable global mental status (Mini-Mental State Exam) who met NINCDS-ADRDA criteria for Alzheimer's disease (AD) were included. Standard neuropsychological tests of naming, intelligence, achievement, verbal fluency, anterograde and remote verbal and visuospatial memory, and motor skill learning were given. The pCBD patient exhibited a progressive asymmetric akinetic-rigid syndrome, which was unresponsive to Sinemet. His initially mild, intellectual deficits consisted of apraxia, slowed speech, and word-finding and memory difficulties. Over a 2-year period, a dementia syndrome developed, which involved more-serious deficits in praxis and naming, as well as impairments in spelling, calculation, verbal fluency, IQ, anterograde verbal and visuospatial memory, and motor skill learning. When tested by recall methods, the pCBD patient exhibited marked deficits on several tests of remote memory; however, on recognition testing, he performed normally on the Famous Faces Test and on a test of geographical knowledge, which measures remote visuospatial memory. By contrast, the four AD patients, who showed equivalent naming difficulties, less-severe fluency deficits, and normal motor skill learning, showed severe impairments in recalling and recognizing the names of famous people from photographs. A magnetic resonance imaging (MRI) scan of the pCBD patient showed marked frontal and parietal lobe atrophy and central atrophy, with ventriculomegaly that was greater on the left side of the brain. The temporal lobes were relatively spared, and the amygdalae, hippocampi, and temporal horns were of normal size.(ABSTRACT TRUNCATED AT 250 WORDS)
在一所大学医学中心,对一名可能患有皮质基底节变性(pCBD)和痴呆症的患者的顺行性和逆行性失忆进行了研究。研究纳入了该pCBD患者以及另外四名全球精神状态(简易精神状态检查表)相当、符合美国国立神经疾病与中风研究所 - 阿尔茨海默病及相关疾病协会(NINCDS - ADRDA)阿尔茨海默病(AD)标准的对照患者。进行了标准的神经心理学测试,包括命名、智力、成就、言语流畅性、顺行性和远期言语及视觉空间记忆以及运动技能学习测试。该pCBD患者表现出进行性不对称运动不能 - 强直综合征,对左旋多巴 - 卡比多巴复方制剂无反应。其最初轻度的智力缺陷包括失用症、言语迟缓、找词困难和记忆障碍。在两年时间里,发展出一种痴呆综合征,涉及更严重的失用症和命名障碍,以及拼写、计算、言语流畅性、智商、顺行性言语和视觉空间记忆及运动技能学习方面的损害。通过回忆方法测试时,该pCBD患者在多项远期记忆测试中表现出明显缺陷;然而,在识别测试中,他在名人面孔测试和一项测量远期视觉空间记忆的地理知识测试中表现正常。相比之下,四名AD患者虽有同等程度的命名困难、不太严重的流畅性缺陷且运动技能学习正常,但在从照片中回忆和识别名人名字方面表现出严重损害。对该pCBD患者的磁共振成像(MRI)扫描显示额叶和顶叶明显萎缩以及中央萎缩,脑室扩大,左侧大脑更为明显。颞叶相对未受影响,杏仁核、海马体和颞角大小正常。(摘要截取自250字)