一例接受利妥昔单抗治疗后病情得到缓解的难治性老年肌无力病例

W. Jeong, Min Ju Kang
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引用次数: 0

摘要

重症肌无力(MG)是一种自身免疫性疾病,其特征是神经肌肉接头处的乙酰胆碱受体产生抗体,从而导致肌无力、疲劳和上睑下垂等各种症状。传统上,MG 主要影响 30 多岁的年轻女性,但最近的趋势表明,无论男女,老年人群的发病率也在不断上升。由于老年人的表现多种多样,而且标准治疗的并发症风险较高,因此老年人 MG 的诊断和管理面临着挑战。利妥昔单抗是一种免疫抑制剂,在难治性 MG 病例中显示出疗效,为治疗提供了一种有前景的选择。在此,我们介绍了一例 82 岁女性阿尔茨海默痴呆患者的病例,她出现全身无力,最终被诊断为 MG。尽管她最初接受了免疫球蛋白治疗,但随后病情复发,而利妥昔单抗治疗使她的症状和功能状态得到了显著改善。我们的病例揭示了老年 MG 诊断的挑战性和治疗的复杂性,并强调了利妥昔单抗是一种有价值的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of refractory myasthenia gravis in the elderly demonstrating remission following rituximab therapy
Myasthenia gravis (MG) is an autoimmune disorder characterized by antibodies against acetylcholine receptors at the neuromuscular junction, leading to various symptoms such as muscle weakness, fatigue, and ptosis. While MG traditionally affects young women in their 30s, recent trends indicate an increasing incidence in the elderly population regardless of gender. Diagnosis and management of MG in the elderly pose challenges due to diverse presentations and higher risks of complications from standard treatments. Rituximab, an immunosuppressive agent, has shown efficacy in refractory MG cases, offering a promising therapeutic option. Here, we present a case of an 82-year-old female with Alzheimer dementia who presented with generalized weakness, ultimately diagnosed with MG. Despite initial treatment with immunoglobulin and subsequent relapse, rit-uximab therapy led to significant improvement in symptoms and functional status. Our case un-derscores the diagnostic challenges and therapeutic complexities of MG in the elderly and highlights rituximab as a valuable treatment option.
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