Suppr超能文献

一名患有抗合成酶综合征的患者出现非典型进行性多灶性白质脑病。

Atypical progressive multifocal leukoencephalopathy in a patient with antisynthetase syndrome.

作者信息

Belhassen-Garcia Moncef, Rábano-Gutiérrez Alberto, Velasco-Tirado Virginia, Romero-Alegria Angela, Pérez-Garcia Maria-Luisa, Martin-Oterino Jose Angel

机构信息

Department of Internal Medicine, Unit of Infectious Diseases. IBSAL. University Hospital of Salamanca. CIETUS, University of Salamanca, Spain.

出版信息

Intern Med. 2015;54(5):519-24. doi: 10.2169/internalmedicine.54.2748. Epub 2015 Jan 15.

Abstract

Antisynthetase syndrome is a disorder belonging to the dermatomyositis/polymyositis group, with high rates of morbidity and mortality. We herein present the case of a 71-year-old man who was diagnosed with antisynthetase syndrome and treated with rituximab. Almost three years later, the patient showed right-sided hemiparesis that ultimately progressed to complete hemiplegia and advancing cognitive deterioration with a poor clinical outcome. The neuropathological diagnosis was progressive multifocal leukoencephalopathy. Treatment with rituximab for antisynthetase syndrome itself plays a fundamental role in the development of infectious complications.

摘要

抗合成酶综合征是一种属于皮肌炎/多肌炎组的疾病,发病率和死亡率很高。我们在此报告一例71岁男性患者,该患者被诊断为抗合成酶综合征并接受了利妥昔单抗治疗。大约三年后,患者出现右侧偏瘫,最终发展为完全性偏瘫,并伴有进行性认知功能减退,临床预后较差。神经病理学诊断为进行性多灶性白质脑病。利妥昔单抗治疗抗合成酶综合征本身在感染性并发症的发生中起重要作用。

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