重症肌无力的综合治疗方案综述。

IF 4.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Alexander J Randall, David J Post
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引用次数: 0

摘要

治疗重症肌无力(MG)的挑战源于多种潜在机制、不同的表现、对慢性免疫治疗的需求以及治疗的长期后果。该病本身的临床表现多种多样,从眼睛下垂到呼吸衰竭。潜在的病因可能是副肿瘤或几种已确定的影响突触后神经肌肉连接的抗体之一。治疗策略取决于所有这些因素。有有限的药物可用于对症治疗神经肌肉交界处,而大多数治疗侧重于免疫疗法,以限制免疫反应。胸腺切除术对大多数胸腺瘤患者和许多抗体阳性疾病患者是有益的。在这种慢性疾病中,选择正确的治疗方法以最大限度地提高疗效并限制药物的不良影响是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comprehensive review of the treatment options in myasthenia gravis.

The challenge of treating of Myasthenia Gravis (MG) stems from the multiple underlying mechanisms, the varied presentations, the need for chronic immunotherapy, and the long-term consequences of treatment. The disease itself is varied with clinical presentations ranging from droopy eyes to respiratory failure. The underlying etiology may be paraneoplastic or one of several identified antibodies that affect the post-synaptic neuromuscular junction. Treatment strategies vary depending on all of these factors. There are limited medications available for symptomatic treatment of the neuromuscular junction while most treatment focuses on immunotherapy to limit the immune response. Thymectomy is beneficial for most patients with thymoma and many with antibody positive disease. Choosing the right treatments to maximize benefits and limit adverse effects of the medicines is crucial in this chronic disease.

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来源期刊
Dm Disease-A-Month
Dm Disease-A-Month 医学-医学:内科
CiteScore
5.70
自引率
2.50%
发文量
140
审稿时长
>12 weeks
期刊介绍: Designed for primary care physicians, each issue of Disease-a-Month presents an in-depth review of a single topic. In this way, the publication can cover all aspects of the topic - pathophysiology, clinical features of the disease or condition, diagnostic techniques, therapeutic approaches, and prognosis.
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