Adult-onset Seizures as the First Manifestation of Anti-dsDNA Negative Systemic Lupus Erythematosus.

Q2 Medicine
Oman Medical Journal Pub Date : 2025-07-31 eCollection Date: 2025-07-01 DOI:10.5001/omj.2025.24
Oladotun Victor Olalusi, Joseph Yaria, Ibukun Dedeke, Ikechukwu Chukwuocha
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引用次数: 0

Abstract

Systemic lupus erythematosus (SLE) is a quintessential autoimmune disease once thought to be rare among Africans. Neuropsychiatric manifestations of SLE range from headaches, mood/behavioral disorders, to seizures. There are documented reports of seizures accompanying the diagnosis of SLE, with varying prevalence according to specific regions. However, seizures rarely precede the diagnosis of SLE. We present a case report of a 19-year-old African woman with adult-onset seizures preceding an overt diagnosis of negative anti-dsDNA SLE. A preceding short course of anti-malarial and carbamazepine prompted early consideration of drug-induced lupus erythematosus. However, the clinical features of SLE progressed and persisted despite their discontinuation. Among high-risk groups, it is important to recognize SLE as a potential cause of adult-onset seizures. In the absence of clear offending agents, metabolic or structural disease, baseline antinuclear antibody may be imperative in the diagnostic workup of such patients.

成人发病癫痫是抗dsdna阴性系统性红斑狼疮的第一表现。
系统性红斑狼疮(SLE)是一种典型的自身免疫性疾病,曾经被认为是罕见的非洲人。SLE的神经精神表现包括头痛、情绪/行为障碍和癫痫发作。有文献报道癫痫发作伴随SLE的诊断,有不同的患病率根据具体地区。然而,癫痫发作很少先于SLE的诊断。我们提出一个病例报告,19岁的非洲妇女与成人发病癫痫发作前的公开诊断为阴性抗dsdna SLE。之前短疗程的抗疟疾和卡马西平提示早期考虑药物性红斑狼疮。然而,尽管停止治疗,SLE的临床特征仍在发展并持续存在。在高危人群中,重要的是要认识到SLE是成人癫痫发作的潜在原因。在没有明确的致病因子、代谢性或结构性疾病的情况下,基线抗核抗体在此类患者的诊断检查中可能是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oman Medical Journal
Oman Medical Journal Medicine-Medicine (all)
CiteScore
3.10
自引率
0.00%
发文量
119
审稿时长
12 weeks
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