Suppr超能文献

重症肌无力合并M蛋白血症和脱髓鞘性神经病:2例报告

Myasthenia Gravis Complicated by M-proteinemia and Demyelinating Neuropathy: A Report of Two Cases.

作者信息

Kawakita Kaiki, Saito Takuya, Kondo Yoshiyuki, Uchiyama Tsuyoshi, Sato Keishiro

机构信息

Department of Neurology, Seirei Hamamatsu General Hospital, Hamamatsu, JPN.

出版信息

Cureus. 2024 Dec 1;16(12):e74886. doi: 10.7759/cureus.74886. eCollection 2024 Dec.

Abstract

Myasthenia gravis (MG) is characterized by weakness and rapid fatigue of voluntary muscles. Here, we present two cases of early-onset MG, complicated with M-proteinemia and demyelinating neuropathy. Case one was diagnosed with MG at age 29, received tacrolimus post-thymectomy, and developed M-proteinemia and demyelinating neuropathies at age 66 before being diagnosed with B-cell lymphoma. Case two was diagnosed with MG at age 21, received immunosuppressive drugs post-thymectomy, and was diagnosed with myelin-associated glycoprotein antibody-associated neuropathy at age 66. Demyelinating neuropathy with M-proteinuria should be considered when motor symptoms worsen in patients with early-onset MG who receive immunosuppressive drugs after thymectomy.

摘要

重症肌无力(MG)的特征是随意肌无力且迅速疲劳。在此,我们报告两例早发型MG病例,其合并有M蛋白血症和脱髓鞘性神经病。病例一在29岁时被诊断为MG,胸腺切除术后接受他克莫司治疗,66岁时在被诊断为B细胞淋巴瘤之前出现了M蛋白血症和脱髓鞘性神经病。病例二在21岁时被诊断为MG,胸腺切除术后接受免疫抑制药物治疗,66岁时被诊断为与髓鞘相关糖蛋白抗体相关的神经病。对于早发型MG患者,在胸腺切除术后接受免疫抑制药物治疗,若运动症状恶化,应考虑伴有M蛋白尿的脱髓鞘性神经病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d03f/11686030/66ed1ae32d9a/cureus-0016-00000074886-i01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验