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线粒体脑肌病伴高乳酸血症和卒中样发作的诊断与治疗策略

Diagnostic and therapeutic strategies for mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes

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【作者】 林岩纪坤乾赵玉英

【Author】 LIN Yan;JI Kun-qian;ZHAO Yu-ying;Department of Neurology, Qilu Hospital of Shandong University;

【通讯作者】 赵玉英;

【机构】 山东大学齐鲁医院神经内科

【摘要】 线粒体脑肌病伴高乳酸血症和卒中样发作(MELAS)是线粒体病最常见的临床亚型。MELAS的临床表现包括卒中样发作、头痛、癫痫、肌无力等,同时还可伴有多系统受累的表现,从而呈现出高度异质性。诊断需结合详细准确的病史、家族史,以及病理、生化和基因检测的结果。治疗需要多学科综合管理,包括药物治疗和营养运动干预。本文总结了MELAS的诊断和治疗方法,旨在帮助临床医生更全面地理解MELAS,从而做到早期诊断并规范化治疗以改善患者长期预后。

【Abstract】 Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes(MELAS) represent the most common clinical subtype of mitochondrial disorders. The clinical manifestations of MELAS include stroke-like episodes, headaches, epilepsy, and muscle weakness while also exhibiting significant heterogeneity through multi-system presentations. Diagnosis necessitates a comprehensive approach involving detailed medical history, accurate family history assessment, and pathological, biochemical, and genetic testing results. Treatment requires a multidisciplinary approach, encompassing pharmacotherapy and nutritional and exercise interventions. This article provides an overview of the diagnostic and therapeutic strategies for MELAS to aid clinicians in gaining a comprehensive understanding of this condition and facilitating early diagnosis and standardized treatment to improve the long-term prognosis of patients.

【基金】 山东省自然科学基金面上项目(ZR2021MH170)
  • 【文献出处】 内科急危重症杂志 ,Journal of Critical Care in Internal Medicine , 编辑部邮箱 ,2024年03期
  • 【分类号】R743.3;R746
  • 【下载频次】52
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