Sartor H, Loose R, Tucha O, Klein H E, Lange K W
Department of Psychiatry, University of Regensburg, Germany.
Acta Neurol Scand. 2002 Nov;106(5):309-13. doi: 10.1034/j.1600-0404.2002.01089.x.
We report on a patient with long standing, full-blown mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS). In contrast to earlier publications, detailed neuropsychological assessment revealed no dementia but a pattern of distinct cognitive deficits with marked impairment of visuo-constructive and executive functions. Focal lesions and progressing atrophy mainly of the basal ganglia and the temporo-parieto-occipital area with preservation of hippocampal and entorhinal structures were present. Furthermore, a 4-year follow-up assessment revealed an increasing deterioration of distinct cognitive functions, including phasic alertness, tactile functions and the discrimination of tone pitch and rhythm. This may be because of chronic regional metabolic disturbances, as there was no further stroke-like episode in that period of time.
我们报告了一例患有长期、典型线粒体脑肌病伴乳酸酸中毒及卒中样发作(MELAS)的患者。与早期出版物不同的是,详细的神经心理学评估显示没有痴呆,但存在一种明显的认知缺陷模式,视觉建构和执行功能有显著损害。存在局灶性病变以及主要是基底神经节和颞顶枕区的进行性萎缩,而海马体和内嗅结构得以保留。此外,一项为期4年的随访评估显示,包括阶段性警觉、触觉功能以及音高和节奏辨别在内的特定认知功能日益恶化。这可能是由于慢性局部代谢紊乱,因为在那段时间没有进一步的卒中样发作。