硫唑嘌呤诱导的系统性红斑狼疮无菌性钩端脑膜炎:一种罕见的表现。

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
BJR Case Reports Pub Date : 2023-09-11 eCollection Date: 2023-10-01 DOI:10.1259/bjrcr.20230063
Mariana Santos, Matheus Alves da Silva, Maria Laura Piassa, Danielly Santos, Alex Machado Baeta, Lázaro Luis Amaral
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种自身免疫性系统性疾病,这些患者可能有神经系统受累;然而,无菌性钩端脑膜炎被认为是一种非常罕见的特征,在1.4-2.0%的患者中观察到。在这里,我们描述了一例年轻男性SLE患者接受硫唑嘌呤治疗并伴有进行性头痛的病例,该病例显示弥漫性后窝钩端脑膜炎,相对保留了幕上隔室,这是一种药物不良反应,是SLE中枢神经系统受累的罕见表现。硫唑嘌呤的治疗中断,开始使用甲基强的松龙,患者的神经状态在5 几天后,在MRI随访中显示软脑膜增强完全消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Aseptic leptomeningitis induced by azathioprine in systemic lupus erythematosus: a rare manifestation.

Aseptic leptomeningitis induced by azathioprine in systemic lupus erythematosus: a rare manifestation.

Aseptic leptomeningitis induced by azathioprine in systemic lupus erythematosus: a rare manifestation.

Systemic lupus erythematosus (SLE) is an autoimmune systemic disease and these patients can have neurological involvement; however, aseptic leptomeningitis is considered to be a very rare feature, observed in 1.4-2.0% of patients. Here, we described a case of a young male with SLE treated with azathioprine with progressive headache, which revealed diffuse posterior fossa leptomeningitis, relatively sparing the supratentorial compartment, that represent an adverse drug reaction - a rare manifestation of central nervous system involvement in SLE. Treatment with azathioprine was interrupted and methylprednisolone was initiated and the patient has significant improvement of his neurological state in 5 days later, demonstrating total involution of the leptomeningeal enhancement on MRI follow-up.

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BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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