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线粒体脑肌病的临床特征及MRI影像诊断分析

作者:李长海

所属单位:河南省信阳市第四人民医院(河南 信阳 464006)

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摘要

目的 研究线粒体脑肌病(ME)的 临床特征和MRI影像诊断分析。方法 选取 我院2011年2月-2015年3月神经内科收治 确诊的18例ME患者,通过脑电图、肌电 图、血液生化检测和影像观察等手段回顾 性分析ME患者的临床特征,并进一步探讨 MRI的影像特征及诊断价值。结果 该18例 ME患者脑电图检测出现16例异常,5例轻 度,7例中度,4例重度;肌电图观有15例 出现肌源性损伤和(或)神经源性损伤;血 液生化检测显示14例LA异常较高,部分患 者伴有CPK、LDH异常升高表达;肌活检显 示12例出现RRF和线粒体异常增多或结构 异常。MRI影像显示16例信号呈T1WI低信 号、T2WI高信号表达;16例病变部位主要 位于大脑皮质和深部脑灰质部,仅少数患 者脑干和白质部位可见受累;有15例显示 有脑萎缩(大小脑)症状。结论 ME临床症 状主要为癫痫、智力障碍和肢体运动受限 等,临床常规检测手段中多表现为脑电 图异常,肌电图肌源性和(或)神经源性 损伤,肌活检RRF核线粒体增多或结构异 常、血液生化检测LA异常较高,部分患者 CPK、LDH异常升高表达等临床特征;MRI 影像具有一定的信号强弱表达特征,且对 显示病变部位和脑萎缩等效果较好,临床 中可结合ME的MRI影像结果和临床特征进 行有效诊断。

Objective To study the clinical features and MRI diagnosis of mitochondrial encephalomyopathies (ME). Methods A total of 18 cases of ME patients admitted to our hospital during February 2011 to March 2015 were enrolled in the study. The clinical features of ME patients were retrospectively analyzed by electroencephalogram (EEG), electromyography (EMG), blood biochemical detection and imaging observation. The MRI findings and diagnosis value were explored. Results Among 18 cases of ME patients, there were 16 cases with abnormal EEG detected, the disease was mild in 5 cases, moderate in 7 cases, and severe in 4 cases. EMG showed 15 cases of myogenic injury and (or) neurogenic injury. Blood biochemical detection showed 14 cases of abnormally high LA, some patients with abnormally increased expression of CPK and LDH. Muscle biopsy showed abnormally increased RRF and mitochondria or structural abnormalities in 12 cases. MRI imaging showed low signal on T1WI and high signal on T2WI in 16 cases. 16 cases of lesions were mainly located in cerebral cortex and deep gray matter, there was involvement of white matter and brainstem in only a minority of patients. 15 cases showed symptoms of brain atrophy. Conclusion The main clinical symptoms of ME include epilepsy, mental disorder and limb movement restriction. In terms of routine clinical detection means, EEG shows abnormalities, EMG shows myogenic and (or) neurogenic injury, muscle biopsy shows increased RRF nuclear mitochondria or structural abnormalities, blood biochemical detection shows abnormally high LA, abnormally high expression of CPK and LDH in some patients. MRI images show certain signal intensity characteristics. It can well display the location of lesions and brain atrophy. In clinical practice, MRI images of ME can be combined with clinical features for effective diagnosis.

【关键词】线粒体脑肌病;病理特征

【中图分类号】R742

【文献标识码】A

【DOI】 10.3969/j.issn.1672- 5131.2017.07.001

前言

ME是一组由线粒体DNA和(或)核DNA缺陷引起线粒体结构和(或)功 能障碍进而导致的以脑和横纹肌受累为主的多系统疾病,多发于青中 年群体且具有较高的母系遗传性,患者临床多表现为突发性脑卒中、 癫痫、智力发育迟缓或明显衰退、身材矮小等症状[1-2]。以往由于ME 较为少见和症状表现缺乏特异性,使得临床较易误诊为脑梗死、癫痫 和脑炎等疾病[3]。近年来随着实验室检查、MRI和CT影像及病理检查等 手段的丰富和改进,引起人们对ME的深入关注,据此我院于2011年2 月~2015年3月对收治的18例ME患者进行系统回顾性分析,旨在探讨ME 的临床病理特征,并进一步分析MRI的影像诊断价值。