Mnif Leila, Sellami Rim, Masmoudi Jawaher
Department of Psychiatry «A», Hédi Chaker University Hospital, Sfax, Tunisia.
Pan Afr Med J. 2015 Dec 4;22:333. doi: 10.11604/pamj.2015.22.333.8288. eCollection 2015.
Leigh syndrome is a mitochondrial encephalomyopathy that occurs due to "cytochrome c oxidase deficiency". Few psychiatric disorders have been defined that are associated with Leigh syndrome. The objective of this work is to study relations between mitochondrial dysfunction and psychiatric disorders. It was a 20 year old male patient, who received Modopar, for severe extra pyramidal symptoms caused by Leigh syndrome. He developed, four months ago, acute psychotic symptoms such as audio-visual hallucinations, persecution and mystic delirium. The cerebral MRI has shown signal abnormalities in central grey nucleus. The EEG recording and blood test were normal. The hypothesis of drug induced psychiatric disorders (Modopar) was possible. The evolution under atypical antipsychotic was only partial. In this case, the cerebrospinal fluid and lactate levels mean that mitochondria were not an overall explanation for these psychiatric disorders but may at least play a partial role. Psychiatric disorders may just be acomorbidity.
Leigh综合征是一种由于“细胞色素c氧化酶缺乏”而发生的线粒体脑肌病。很少有与Leigh综合征相关的精神障碍被明确界定。这项工作的目的是研究线粒体功能障碍与精神障碍之间的关系。这是一名20岁男性患者,因Leigh综合征导致的严重锥体外系症状而接受美多巴治疗。他在四个月前出现了急性精神病症状,如视听幻觉、被害妄想和神秘妄想。脑部磁共振成像显示中央灰质核有信号异常。脑电图记录和血液检查正常。药物诱发精神障碍(美多巴)的假设是有可能的。使用非典型抗精神病药物治疗后的病情改善只是部分有效。在这种情况下,脑脊液和乳酸水平表明线粒体并非这些精神障碍的全部病因,但至少可能起到部分作用。精神障碍可能只是一种共病。