Case report: Intravascular large B cell lymphoma mimicking acute demyelinating encephalomyelitis after SARS-CoV-2 reinfection: diagnostic value of advanced MRI techniques and the literature review with the assistance of ChatGPT.

IF 5.9 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2024-11-14 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1478163
Sujuan Chen, Mingchen Cai, Guirong Tan, Ruomi Guo, Qiong Liang, Hainan Li, Xiang Liu
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Abstract

The intravascular large B cell lymphoma (IVLBCL) is a rare subtype of lymphoma. The IVBCL is usually found with systemic involvement, with a relative predilection for skin and the central nervous system (CNS), followed by a rapidly progressive course and poor prognosis with a high mortality rate. IVLBCL is difficult to diagnose based on conventional MRI alone. Herein, we presented a previously healthy 59-year-old woman who developed hemiparesis and altered mental status after her reinfection of SARS-CoV-2. The initial MRI revealed non-enhancing lesions in the splenium of the corpus callosum (CC), periventricular, and bilateral subcortical white matter with hyperintensity on diffusion weighted imaging (DWI). The patient was diagnosed with subacute infarction, and she was treated with antithrombotic therapy. Her neurological symptoms continued to deteriorate, and she developed unconsciousness. Her CSF test showed elevated white cell count and positive oligoclonal bands. The follow-up MRI was scanned 16 days later. Compared to the initial MRI, the periventricular and bilateral subcortical lesions enlarged on conventional MRI. The post-contrast 3D black blood Cube images demonstrated multiple parenchymal and diffuse meningeal enhancements and 3D arterial spin labeling showed increased perfusion in the CC splenium. These findings suggested the differential diagnosis of acute demyelinating encephalomyelitis (ADEM) after SARS-CoV-2 reinfection, versus intravascular lymphoma. After the treatment of intravenous immunoglobulin and methylprednisolone, her symptoms significantly improved. The second follow-up MRI two weeks later detected a new unenhanced lesion in the left temporal lobe. A brain biopsy was performed and IVLBCL was diagnosed. We reviewed the brain MRI findings of IVLBCL in the literature with the assistance of ChatGPT. Although less specific, the imaging features including "high signal lesions on DWI, meningeal thickening and enhancement, and masslike lesions" highly suggested the possibility of IVLBCL. The biopsy should be planned after imaging progression. The association between IVLBCL and SARS-CoV-2 reinfection is undefined.

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病例报告:SARS-CoV-2再感染后血管内大B细胞淋巴瘤模拟急性脱髓鞘性脑脊髓炎:先进MRI技术的诊断价值及ChatGPT辅助下的文献复习
血管内大B细胞淋巴瘤(IVLBCL)是一种罕见的淋巴瘤亚型。IVBCL通常累及全身,相对偏爱皮肤和中枢神经系统(CNS),随后病程进展迅速,预后差,死亡率高。IVLBCL仅靠常规MRI很难诊断。在此,我们报告了一名先前健康的59岁女性,她在再次感染SARS-CoV-2后出现偏瘫和精神状态改变。初始MRI显示胼胝体(CC)脾、脑室周围和双侧皮质下白质无强化病变,弥散加权成像(DWI)呈高信号。患者被诊断为亚急性梗死,并接受抗血栓治疗。她的神经系统症状持续恶化,并逐渐失去知觉。脑脊液检查显示白细胞计数升高,寡克隆带阳性。16天后进行后续MRI扫描。与最初的MRI相比,常规MRI显示脑室周围和双侧皮质下病变扩大。增强后的3D黑血立方图像显示多发性实质和弥漫性脑膜增强,3D动脉自旋标记显示CC脾灌注增加。这些发现提示了SARS-CoV-2再感染后急性脱髓鞘性脑脊髓炎(ADEM)与血管内淋巴瘤的鉴别诊断。经静脉注射免疫球蛋白和甲基强的松龙治疗后,患者症状明显改善。两周后的第二次后续MRI检查在左颞叶发现了一个新的未增强的病变。行脑活检,诊断为IVLBCL。我们在ChatGPT的帮助下回顾了文献中IVLBCL的脑MRI表现。虽然特异性不强,但“DWI高信号病灶、脑膜增厚强化、团块样病灶”等影像学特征提示IVLBCL的可能性较高。活检应在影像学进展后计划。IVLBCL与SARS-CoV-2再感染之间的关系尚不明确。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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