一例年轻女性脑干脑炎并发系统性红斑狼疮的病例报告

Muhammad Nawaz Khan , Muniba Fatima , Muhammad Mubashir , Syed Muhammad Sinaan Ali
{"title":"一例年轻女性脑干脑炎并发系统性红斑狼疮的病例报告","authors":"Muhammad Nawaz Khan ,&nbsp;Muniba Fatima ,&nbsp;Muhammad Mubashir ,&nbsp;Syed Muhammad Sinaan Ali","doi":"10.1016/j.glmedi.2024.100145","DOIUrl":null,"url":null,"abstract":"<div><div>We present a rare case of autoimmune brainstem encephalitis, a serious inflammatory condition affecting the brainstem, in a 20-year-old female simultaneously with systemic lupus erythematosus (SLE). Brainstem encephalitis can be caused by various infectious diseases, autoimmune disorders, and paraneoplastic syndromes. When associated with autoimmune disorders, its diagnosis and management can be challenging.Symptoms typically include those of the underlying autoimmune disorder, along with features of encephalitis such as headache, altered consciousness, fever, seizures, and cranial nerve involvement. Our patient presented with fever, seizures, and signs indicative of SLE, which were later confirmed through various antibody profiles. The patient was treated with steroids and immunosuppressants, showing a positive response, and was eventually discharged. This case highlights the diagnostic challenges and treatment approaches employed to manage symptoms and address the disease. Autoimmune brainstem encephalitis caused by SLE is a rare but potentially morbid condition, often diagnosed late. Looking out for specific signs and symptoms leads to prompt diagnosis and timely management. SLE encephalitis is rarely reported and poorly understood.Therefore, further research is required.</div></div>","PeriodicalId":100804,"journal":{"name":"Journal of Medicine, Surgery, and Public Health","volume":"4 ","pages":"Article 100145"},"PeriodicalIF":0.0000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A case report of brainstem encephalitis associated with systemic lupus erythematosus in a young female\",\"authors\":\"Muhammad Nawaz Khan ,&nbsp;Muniba Fatima ,&nbsp;Muhammad Mubashir ,&nbsp;Syed Muhammad Sinaan Ali\",\"doi\":\"10.1016/j.glmedi.2024.100145\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We present a rare case of autoimmune brainstem encephalitis, a serious inflammatory condition affecting the brainstem, in a 20-year-old female simultaneously with systemic lupus erythematosus (SLE). Brainstem encephalitis can be caused by various infectious diseases, autoimmune disorders, and paraneoplastic syndromes. When associated with autoimmune disorders, its diagnosis and management can be challenging.Symptoms typically include those of the underlying autoimmune disorder, along with features of encephalitis such as headache, altered consciousness, fever, seizures, and cranial nerve involvement. Our patient presented with fever, seizures, and signs indicative of SLE, which were later confirmed through various antibody profiles. The patient was treated with steroids and immunosuppressants, showing a positive response, and was eventually discharged. This case highlights the diagnostic challenges and treatment approaches employed to manage symptoms and address the disease. Autoimmune brainstem encephalitis caused by SLE is a rare but potentially morbid condition, often diagnosed late. Looking out for specific signs and symptoms leads to prompt diagnosis and timely management. SLE encephalitis is rarely reported and poorly understood.Therefore, further research is required.</div></div>\",\"PeriodicalId\":100804,\"journal\":{\"name\":\"Journal of Medicine, Surgery, and Public Health\",\"volume\":\"4 \",\"pages\":\"Article 100145\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-10-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medicine, Surgery, and Public Health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949916X24000987\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medicine, Surgery, and Public Health","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949916X24000987","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

我们介绍了一例罕见的自身免疫性脑干脑炎病例,这是一种影响脑干的严重炎症,患者是一名 20 岁的女性,同时患有系统性红斑狼疮(SLE)。脑干脑炎可由各种传染病、自身免疫性疾病和副肿瘤综合征引起。症状通常包括潜在的自身免疫性疾病的症状,以及脑炎的特征,如头痛、意识改变、发热、癫痫发作和颅神经受累。我们的患者出现发热、癫痫发作和系统性红斑狼疮的体征,后经各种抗体检查证实为系统性红斑狼疮。患者接受了类固醇和免疫抑制剂治疗,显示出积极的反应,最终康复出院。该病例凸显了诊断方面的挑战以及为控制症状和治疗疾病而采用的治疗方法。系统性红斑狼疮引起的自身免疫性脑干脑炎是一种罕见的疾病,但可能会导致死亡,而且往往诊断较晚。注意特定的体征和症状有助于及时诊断和治疗。系统性红斑狼疮脑炎鲜有报道,人们对其了解甚少。
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 report of brainstem encephalitis associated with systemic lupus erythematosus in a young female
We present a rare case of autoimmune brainstem encephalitis, a serious inflammatory condition affecting the brainstem, in a 20-year-old female simultaneously with systemic lupus erythematosus (SLE). Brainstem encephalitis can be caused by various infectious diseases, autoimmune disorders, and paraneoplastic syndromes. When associated with autoimmune disorders, its diagnosis and management can be challenging.Symptoms typically include those of the underlying autoimmune disorder, along with features of encephalitis such as headache, altered consciousness, fever, seizures, and cranial nerve involvement. Our patient presented with fever, seizures, and signs indicative of SLE, which were later confirmed through various antibody profiles. The patient was treated with steroids and immunosuppressants, showing a positive response, and was eventually discharged. This case highlights the diagnostic challenges and treatment approaches employed to manage symptoms and address the disease. Autoimmune brainstem encephalitis caused by SLE is a rare but potentially morbid condition, often diagnosed late. Looking out for specific signs and symptoms leads to prompt diagnosis and timely management. SLE encephalitis is rarely reported and poorly understood.Therefore, further research is required.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信