与猴痘病毒相关的中枢神经系统神经炎性疾病:系统综述和行动呼吁。

IF 8.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMC Medicine Pub Date : 2025-02-12 DOI:10.1186/s12916-025-03921-6
Shramana Deb, Ritwick Mondal, Purbita Sen, Dipanjan Chowdhury, Shramana Sarkar, Granthik Banerjee, Vramanti Sarkar, Anjan Chowdhury, Julián Benito-León
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引用次数: 0

摘要

背景:猴痘病毒(MPXV)已成为一个重大的全球卫生问题,在世界各地暴发。虽然MPXV主要以其皮肤和全身表现而闻名,但它也可引起中枢神经系统(CNS)并发症。本系统综述描述了mpxv相关中枢神经系统炎症性疾病的人口学、临床、诊断和治疗特点。方法:我们系统地回顾文献,以确定mpxv相关的中枢神经系统神经炎症性疾病的病例。提取和分析人口统计学、系统和神经学表现、诊断方法、治疗策略和结果的数据。结果:18例mpxv相关神经炎性疾病。患者平均年龄27.8岁(28天~ 43岁),男性居多(66.7%)。诊断:最常见的诊断为急性播散性脑脊髓炎9例(50.0%),脑炎/脑膜脑炎7例(38.9%),孤立性横脊髓炎1例(5.6%),横脊髓炎合并脑炎1例(5.6%)。从出现全身性症状到神经系统受累的平均潜伏期为6.2天。18例病例中有13例(72.2%)检测到MPXV,主要采用各种生物标本的实时定量聚合酶链反应。在12例有治疗记录的病例中,最常用的治疗方法是替科维马(58.3%)和静脉注射甲基强的松龙(66.7%)。17例报告了结果,29.4%的患者完全恢复,41.2%的患者部分恢复,29.4%的患者死亡。结论:mpxv相关的中枢神经系统神经炎性疾病是罕见的,但会引起明显的并发症。研究结果强调了临床警惕、先进的诊断方法和有针对性的治疗策略的必要性。进一步的研究对于阐明MPXV神经毒性的机制和开发对这些危及生命的疾病的有效治疗是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Neuroinflammatory disorders of the central nervous system associated with monkeypox virus: a systematic review and call to action.

Background: Monkeypox virus (MPXV) has emerged as a significant global health concern with outbreaks worldwide. While MPXV is primarily known for its dermatological and systemic manifestations, it can also cause central nervous system (CNS) complications. This systematic review describes the demographic, clinical, diagnostic, and therapeutic characteristics of MPXV-associated CNS neuroinflammatory disorders.

Methods: We systematically reviewed the literature to identify cases of MPXV-associated CNS neuroinflammatory disorders. Data on demographics, systemic and neurological manifestations, diagnostic methods, treatment strategies, and outcomes were extracted and analyzed.

Results: Eighteen cases of MPXV-associated neuroinflammatory disorders were identified. The mean age of patients was 27.8 years (range: 28 days to 43 years), with a male predominance (66.7%). Diagnosis included The most common diagnoses were acute disseminated encephalomyelitis in nine cases (50.0%), encephalitis/meningoencephalitis in seven cases (38.9%, isolated transverse myelitis in one case (5.6%), and transverse myelitis with encephalitis in one case (5.6%). The latency between the onset of systemic symptoms and neurological involvement averaged 6.2 days. MPXV detection was confirmed in 13 of 18 (72.2%) cases, primarily using quantitative real-time polymerase chain reaction from various biological specimens. Among the 12 cases with documented treatment, the most commonly administered therapies were tecovirimat (58.3%) and intravenous methyl-prednisolone (66.7%). Outcomes were reported in 17 cases, with complete recovery in 29.4%, partial recovery in 41.2%, and death in 29.4% of patients.

Conclusions: MPXV-associated neuroinflammatory disorders of the CNS are rare but cause significant complications. The findings underscore the need for clinical vigilance, advanced diagnostic approaches, and targeted therapeutic strategies. Further research is essential to elucidate mechanisms underlying MPXV neurovirulence and develop effective treatments for these life-threatening conditions.

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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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