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一名成年患者出现典型影像学表现和独特脑脊液特征的急性坏死性脑病:病例报告

Acute necrotizing encephalopathy in an adult presenting with typical imaging findings and distinctive cerebrospinal fluid characteristics: a case report.

作者信息

Wang Yan, He Mianwang, Zhao Hong, Yang Fei, Zhang Jiatang, Yu Shengyuan

机构信息

The First Medical Center, Department of Neurology, Chinese PLA General Hospital, Fuxing Road 28, Haidian District, Beijing, 100853, China.

出版信息

J Med Case Rep. 2025 Mar 8;19(1):104. doi: 10.1186/s13256-025-05147-9.

DOI:10.1186/s13256-025-05147-9
PMID:40057771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11889806/
Abstract

BACKGROUND

Acute necrotizing encephalopathy is a rare, clinically distinct subgroup of acute encephalopathy, which may be a complication of coronavirus disease 2019.

CASE PRESENTATION

A 22-year-old male of Han Chinese with a yellow complexion presented with fever, psychological and behavioral abnormalities, seizures, and coma. Cerebrospinal fluid tests indicated leukocytosis, high protein concentrations, and significantly elevated levels of neuron-specific enolase, interleukin-2, interleukin-6, and interleukin-8. Magnetic resonance imaging revealed restricted diffusion in the bilateral thalami and splenium of the corpus callosum, and no hemorrhagic signals were detected on susceptibility-weighted imaging. Hyperintense and hypointense lesions in the bilateral thalami, brainstem, cerebellum, and splenium of the corpus callosum were observed in T1- and T2-weighted sequences without gadolinium enhancement. At the 6-month follow-up, the T1 and T2 sequences showed significant atrophy in the cerebellar hemispheres and brachium pontis and an enlarged fourth ventricle. After symptomatic and immunotherapy treatment, the prognosis was good.

CONCLUSION

We report a rare case of a 22-year-old male diagnosed acute necrotizing encephalopathy showing typical imaging findings and distinctive cerebrospinal fluid presentation. In adults, heightened awareness of acute necrotizing encephalopathy is crucial because early recognition and treatment have the potential to enhance prognosis.

摘要

背景

急性坏死性脑病是急性脑病中一种罕见的、临床特征明显的亚组疾病,可能是新型冠状病毒肺炎的并发症。

病例报告

一名22岁面色发黄的汉族男性,出现发热、心理和行为异常、癫痫发作及昏迷。脑脊液检查显示白细胞增多、蛋白浓度升高,神经元特异性烯醇化酶、白细胞介素-2、白细胞介素-6和白细胞介素-8水平显著升高。磁共振成像显示双侧丘脑及胼胝体压部弥散受限,磁敏感加权成像未检测到出血信号。在T1加权和T2加权序列上观察到双侧丘脑、脑干、小脑及胼胝体压部有高信号和低信号病变,无钆增强。在6个月的随访中,T1和T2序列显示小脑半球和脑桥臂明显萎缩,第四脑室扩大。经过对症和免疫治疗后,预后良好。

结论

我们报告了一例罕见的22岁男性诊断为急性坏死性脑病的病例,其显示出典型的影像学表现和独特的脑脊液表现。在成人中,提高对急性坏死性脑病的认识至关重要,因为早期识别和治疗有可能改善预后。

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