什么是肌病文献?

Tawfiq Al-Lahham, David Lacomis
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引用次数: 0

摘要

摘要:我们报道了2019冠状病毒病相关的重症监护病房获得性神经肌肉疾病。这些患者的结果可能比预期的要差,有一些证据表明2019年冠状病毒病直接导致肌病。糖皮质激素治疗杜氏肌营养不良包括肺和心脏功能的结果。最近的一篇文章指出,杜氏肌营养不良症的诊断持续延迟。一个有趣的报告加那利群岛队列患者与眼咽肌萎缩症进行了讨论。本文提供了一系列肢体带状肌营养不良R12(无色散性肌病)和特发性炎性肌病误诊患者的特征和临床要点。关于自身免疫性肌病的最后一部分包括与肌炎特异性抗体和皮肌炎相关的临床和病理特征的文章,明尼苏达州奥姆斯特德县免疫介导的坏死性肌病(IMNMs)的流行病学,以及德国羟基-3-甲基戊二酰辅酶a还原酶相关IMNM队列的特征。最近的一篇文章提出了早期静脉注射免疫球蛋白对IMNM成人患者的益处。我们还报告了2例不寻常的反信号识别颗粒肌病,表现为不对称的远端无力。
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What Is in the Myopathy Literature?

Abstract: We cover intensive care unit-acquired neuromuscular disorders associated with coronavirus disease 2019. Outcomes may be worse than expected in these patients, and there is some evidence that coronavirus disease 2019 causes myopathy directly. Corticosteroid regimens in Duchenne muscular dystrophy are addressed including outcomes in pulmonary and cardiac function. A recent article notes a continued diagnostic delay in Duchenne muscular dystrophy. An interesting report of a Canary Islands cohort of patients with oculopharyngeal muscular dystrophy is discussed. Features and clinical pearls related to a series of patients with limb-girdle muscle dystrophy R12 (anoctaminopathy) and a misdiagnosis of idiopathic inflammatory myopathy are provided. The last section on autoimmune myopathy includes articles on clinical and pathologic features associated with myositis-specific antibodies and dermatomyositis, the epidemiology of immune-mediated necrotizing myopathies (IMNMs) in Olmsted County, Minnesota, and features of a German cohort of hydroxy-3-methylglutaryl coenzyme A reductase-associated IMNM. A recent article proposes the benefit of early intravenous immunoglobulin use for adults with IMNM. We also highlight a report of 2 unusual cases of antisignal recognition particle myopathy presenting with asymmetric distal weakness.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
期刊最新文献
Acute Multiple Cranial Neuropathies in Chronic Inflammatory Demyelinating Polyneuropathy: A Case Report and Scoping Review of the Literature. Diagnosing X-Linked Myopathy With Excessive Autophagy After 30 years: Genetic, Ultrasonographic, and Electrodiagnostic Findings. Diverse Phenotypic Presentation of the Welander Distal Myopathy Founder Mutation, With Myopathy and Amyotrophic Lateral Sclerosis in the Same Family. Fluoroquinolone-Induced Demyelinating Polyneuropathy. Progressive Multifocal Leukoencephalopathy in Myasthenia Gravis With Selective Hypogammaglobulinemia.
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