Unique presentation of acute neuro-Behçet's disease involving a cytotoxic edema core surrounded by vasogenic edema.

IF 0.9 Q4 RHEUMATOLOGY Modern rheumatology case reports Pub Date : 2024-06-14 DOI:10.1093/mrcr/rxae032
Shohei Yamashita, Daiki Fujimori, Shigemoto Igari, Yusuke Yamamoto, Takahiro Mizuuchi, Hiroaki Mori, Haeru Hayashi, Koichiro Tahara, Tetsuji Sawada
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Abstract

A 53-year-old woman with recurrent stomatitis, genital ulcers, and folliculitis was admitted to our hospital after experiencing visual disturbances for the past two weeks, and a non-throbbing headache for the past three days. She had also developed numbness in her left extremities. An ophthalmological examination revealed inflammatory changes in the eye. Cerebrospinal fluid analysis showed increased cell counts, protein, and interleukin-6 levels. Brain magnetic resonance imaging revealed multiple high signal intensities on T2-weighted (T2W)/fluid-attenuated inversion recovery (FLAIR) images of the pons and occipital and parietal lobes. The T2W/FLAIR high-signal-intensity lesion in the pons was hyperintense on diffusion-weighted imaging (DWI) and hypointense on apparent diffusion coefficient mapping (ADC), suggesting cytotoxic edema. Another high-signal-intensity lesion on T2W/FLAIR was isointense to hyperintense on DWI and hyperintense on ADC, indicating vasogenic edema. The vasogenic edema in the left occipital lobe contained a small core that was hyperintense on DWI and hypointense on ADC, suggesting cytotoxic edema. The patient was diagnosed with acute neuro-Behçet's disease (neuro-BD) and responded well to high-dose glucocorticoid and colchicine treatment. The present report emphasizes that patients with acute neuro-BD may present with cytotoxic edema in the pons and cerebral spheres. Further reports of similar cases would contribute to a better understanding of the role of cytotoxic edema in the pathophysiology of neuro-BD and help elucidate the mechanisms underlying a unique presentation characterized by a central cytotoxic edema core within vasogenic edema. (233 words).

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急性神经性贝赫切特病的独特表现:细胞毒性水肿核心被血管源性水肿包围。
一位 53 岁的女性因反复发作口腔炎、生殖器溃疡和毛囊炎,在过去两周内出现视力障碍,并在过去三天内出现非刺痛性头痛,被送入我院。她还出现了左侧肢体麻木的症状。眼科检查发现她的眼睛有炎症变化。脑脊液分析显示细胞计数、蛋白质和白细胞介素-6水平升高。脑磁共振成像显示,脑桥、枕叶和顶叶的T2加权(T2W)/流体增强反转恢复(FLAIR)图像上出现多个高信号强度。脑桥的T2W/FLAIR高信号强度病变在弥散加权成像(DWI)上呈高密度,而在表观弥散系数图谱(ADC)上呈低密度,表明存在细胞毒性水肿。另一个 T2W/FLAIR 高信号强度病变在 DWI 上呈等密度至高密度,在 ADC 上呈高密度,表明存在血管源性水肿。左枕叶的血管源性水肿包含一个小核心,DWI呈高密度,ADC呈低密度,提示细胞毒性水肿。患者被诊断为急性神经-贝赫切特病(neuro-BD),对大剂量糖皮质激素和秋水仙碱治疗反应良好。本报告强调,急性神经-贝赫切特病患者可能会出现脑桥和脑球细胞毒性水肿。更多类似病例的报告将有助于更好地理解细胞毒性水肿在神经-BD病理生理学中的作用,并有助于阐明以血管源性水肿中的中央细胞毒性水肿核心为特征的独特表现的机制。(233个字)。
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