急性出血性脑白质炎的磁共振成像谱分析:附4例报告。

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Ankit Shukla, Nishant Nayyar, Pooja Kumari, Ankush Kumar, Preeti Takkar
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引用次数: 0

摘要

背景:急性出血性脑白质炎(AHLE),也称为韦斯顿-赫斯特综合征,是一种非常罕见的暴发性脱髓鞘疾病。它被认为是急性播散性脑脊髓炎的超急性和严重变种。临床上,患者表现为发热、头痛、癫痫发作和感觉改变,可迅速发展为昏迷或死亡。磁共振成像(MRI)是诊断AHLE的首选方法,在AHLE的诊断中起着关键作用。本文的目的是让读者熟悉AHLE的典型MRI特征,并讨论其区别。病例总结:本病例系列报告了4例诊断为AHLE的患者的临床表现和典型的神经影像学表现。所有患者均出现急性神经系统症状,如严重头痛、癫痫发作和意识改变,常伴有发热史,提示感染性病因。此外,实验室调查显示,脑脊液分析显示血清炎症标志物和中性粒细胞增多症水平升高,支持感染后病因。MRI结果一致显示特征性白质病变伴出血灶和血管源性水肿,表明AHLE的广泛脱髓鞘特征。结果各不相同,有两名患者幸存下来,但经历了神经系统后遗症,而另外两名不幸死于这种疾病。本病例系列的临床资料、实验室结果和影像学结果与先前发表的研究进行了系统比较。临床表现、影像学特征和结果的主要异同以表格形式呈现。结论:AHLE具有较高的发病率和死亡率,强调早期发现、及时干预和多学科管理的必要性。需要进一步的研究来解释AHLE的病理生理机制,确定早期诊断的潜在生物标志物,并开发靶向治疗来改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnetic resonance imaging spectrum of acute hemorrhagic leukoencephalitis: Four case reports.

Background: Acute hemorrhagic leukoencephalitis (AHLE), also known as Weston-Hurst syndrome, is a very rare and fulminant form of demyelinating disorder. It is considered a hyperacute and severe variant of acute disseminated encephalomyelitis. Clinically, patients present with fever, headache, seizures, and altered sensorium, which can rapidly progress to coma or death. Magnetic resonance imaging (MRI) is the investigation of choice and plays a pivotal role in diagnosing AHLE. The purpose of this article is to make readers familiar with the typical MRI features of AHLE and to discuss differentials.

Case summary: This case series reports the clinical presentation and typical neuroimaging findings in four patients diagnosed with AHLE. All patients presented with acute neurological symptoms, such as severe headaches, seizures, and altered consciousness, often following a history of fever suggesting an infectious etiology. Additionally, laboratory investigations demonstrated elevated levels of serum inflammatory markers and neutrophilic pleocytosis on cerebrospinal fluid analysis, supporting a post-infectious etiology. MRI findings consistently revealed characteristic white matter lesions with hemorrhagic foci and vasogenic edema, indicative of widespread demyelination characteristic of AHLE. The outcomes varied, with two patients surviving but experiencing neurological sequelae, while two others unfortunately succumbed to the disease. The clinical data, laboratory results, and imaging findings from this case series were systematically compared with those from previously published studies. The key similarities and differences in clinical presentation, imaging characteristics, and outcomes are presented in a tabulated format.

Conclusion: AHLE is associated with high morbidity and mortality rates, emphasizing the need for early recognition, prompt intervention, and multidisciplinary management. Further research is needed to explain the pathophysiological mechanisms underlying AHLE, identify potential biomarkers for early diagnosis, and develop targeted therapies to improve patient outcomes.

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来源期刊
World Journal of Clinical Cases
World Journal of Clinical Cases Medicine-General Medicine
自引率
0.00%
发文量
3384
期刊介绍: The World Journal of Clinical Cases (WJCC) is a high-quality, peer reviewed, open-access journal. The primary task of WJCC is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of clinical cases. In order to promote productive academic communication, the peer review process for the WJCC is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJCC are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in clinical cases.
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