托珠单抗和霉酚酸酯成功治疗难治性神经甜味疾病。

Sungeun Hwang, Hyoshin Son, Jangsup Moon, Soon-Tae Lee, Keun Hwa Jung, Kyung-Il Park, Sang Kun Lee, Kon Chu
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引用次数: 0

摘要

甜综合征,或急性发热性中性粒细胞皮肤病,主要是一种皮肤病,表现为红斑斑块;然而,中性粒细胞浸润多个系统。神经-甜病是甜综合征的神经学表现,是复发性无菌性脑膜脑炎的罕见病因,需要与神经- behet病区分开来。虽然神经性甜味疾病通常对皮质类固醇反应良好,但复发的神经性甜味疾病并不是例外情况。在此,我们报告一例51岁男性复发性脑炎并发红斑斑块。患者经皮肤活检证实为Sweet综合征,对皮质类固醇有部分反应。静脉注射免疫球蛋白、利妥昔单抗、托珠单抗和霉酚酸酯后,患者神经系统症状完全恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Refractory neuro-Sweet disease successfully treated with tocilizumab and mycophenolate mofetil.

Refractory neuro-Sweet disease successfully treated with tocilizumab and mycophenolate mofetil.

Refractory neuro-Sweet disease successfully treated with tocilizumab and mycophenolate mofetil.

Refractory neuro-Sweet disease successfully treated with tocilizumab and mycophenolate mofetil.

Sweet syndrome, or acute febrile neutrophilic dermatosis, is mainly a dermatologic condition presenting with erythematous plaques; however, neutrophils infiltrate multiple systems. Neuro-Sweet disease is a neurological manifestation of Sweet syndrome and a rare cause of recurrent aseptic meningoencephalitis, which needs to be distinguished from neuro-Behçet disease. Although neuro-Sweet disease generally responds well to corticosteroids, relapsing neuro-Sweet disease is not an exceptional case. Herein, we present a case of a 51-year-old male with recurrent encephalitis followed by erythematous plaques. The patient was confirmed as Sweet syndrome based on skin biopsy and showed partial response to corticosteroids. With intravenous immunoglobulin, rituximab, tocilizumab, and mycophenolate mofetil, his neurologic symptoms were fully recovered.

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