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MRI/1H-MRS在MELAS综合征与卒中鉴别诊断中的应用研究 被引量:2

Application of MRI/MRS in differential diagnosis of MELAS syndrome and stroke
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摘要 目的 探讨线粒体脑肌病伴高乳酸血症及卒中样发作(MELAS)综合征头颅磁共振(MRI)及头颅磁共振波谱(1H-MRS)特点与其早期诊断价值。方法 对8例诊断为MELAS综合征患者的MRI及MRS结果进行分析。结果 8例MELAS综合征患者的头颅MRI结果示病变累及多个脑叶,主要包括额叶、颞叶、顶叶、枕叶皮质及双侧基底核、放射冠区,其中4例患者可见不同程度的脑萎缩;头颅磁共振血管造影(MRA)检测均未见颅内动脉异常,且病灶区域与主要供血动脉分布无明显相关性;4例患者头颅1H-MRS可见病变区域显著Lac峰,以及病灶区NAA峰显著降低。结论 头颅1H-MRS能够为MELAS综合征患者提供无创性检查,分析脑组织能量代谢变化,对MELAS综合征的早期诊断具有重要价值。 Objective To explore the magnetic resonance imaging(MRI)and magnetic resonancespectroscopy(1H-MRS)characteristics of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-likeepisodes(MELAS)syndrome and the value of application of MRI/MRS in early diagnosis. Method The resultsof MRI and 1H-MRS scans were analyzed in 8 patients of MELAS syndrome. Results The results of MRI scan of 8patients showed that the lesions in the brains were mainly located in frontal lobe, temporal lobe, parietal lobe, occipitallobe, basal ganglia and corona area, and brain atrophy was found in 4 patients. The results of MRA indicated that therewere no intracranial macroangiopathy, and the lesions were not distributed in accordance with cerebral vessels. Theresults of 1H-MRS in the brains of 4 patients showed increased lactate peak and reduced N acetyl aspartate(NAA)peak in the lesions. Conclusion Brain MRI/1H-MRS was an important noninvasive method to analyze the variation ofenergy metabolism, which played an important role in the early diagnosis of MELAS syndrome.
作者 朱晓蕾 武文博 金佳丽 刘卓 牛丰南 ZHU Xiao-lei;WU Wen-bo;JIN Jia-li;LIU Zhuo;NIU Feng-nan(Department of Neurology, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Jiangsu 210000, China)
出处 《脑与神经疾病杂志》 2016年第10期603-607,共5页 Journal of Brain and Nervous Diseases
基金 国家自然科学基金(81300977 81300988 81200839)
关键词 MELAS综合征 磁共振及波谱 早期诊断 MELAS syndrome MRI and 1H-MRS Early diagnoses
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  • 1Barkovich AJ,Good WV,Koch TK,et al. Mitochondrial disorders:analysis of their clinical and imaging characteristics[J]. AJNR AmJ Neuroradiol,1993,14(5): 1119-1137. 被引量:1
  • 2Sproule DM,Kaufmann P. Mitochondrial encephalopathy,lacticacidosis,and stroke like episodes: basic concepts,clinicalphenotype,and therapeutic management of MELAS syndrome[J].Ann N Y Acad Sci,2008,1142: 133-158. 被引量:1
  • 3Kang HC,Lee YM,Kim HD. Mitochondrial disease and epilepsy[J].Brain Dev,2013,35(8): 757-761. 被引量:1
  • 4Weiduschat N,Kaufmann P,Mao X,et al. Cerebral metabolicabnormalities in A3243G mitochondrial DNA mutation carriers[J].Neurology,2014,82(9): 798-805. 被引量:1
  • 5Tsujikawa T,Yoneda M,Shimizu Y,et al. Pathophysiologicevaluation of MELAS strokes by serially quantified MRS and CASLperfusion images[J]. Brain Dev,2010,32(2): 143-149. 被引量:1
  • 6Saneto RP,Friedman SD,Shaw DW. Neuroimaging of MitochondrialDisease[J]. Mitochondrion,2008,8(5-6): 396-413. 被引量:1
  • 7Lorenzoni PJ,Scola RH,Kay CS,et al. MELAS: clinical features,muscle biopsy and molecular genetics[ J]. Arq Neuropsiquiatr,2009,67(3): 668-676. 被引量:1
  • 8黄春元,杨智云,许朝璇,侯瑜,陈素云,吴倩红,赵志清,罗帝林.MELAS型线粒体脑肌病的多模态MRI诊断[J].中国临床医学影像杂志,2014,25(8):533-537. 被引量:12
  • 9Abe K,Yoshimura H,Tanaka H,et al. Comparison of conventional and diffusion-weighted MRI and proton MR spectroscopy in patients with mitochondrial encephalomyopathy,lactic acidosis,and strokelike events[J]. Neuroradiology,2004,46(2): 113-117. 被引量:1
  • 10Cross JH,Gadian DG,Connelly A,et al. Proton magneticresonance spectroscopy studies in lactic acidosis and mitochondrialdisorders[J]. J Inherit Metab Dis,1993,16(4): 800-811. 被引量:1

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