Clinical Problem Solving: A 38-year-Old Woman With Systemic Lupus Erythematosus Presenting With Headache, Nausea, and Vomiting.

IF 0.9 Q4 CLINICAL NEUROLOGY
Neurohospitalist Pub Date : 2023-10-01 Epub Date: 2023-06-08 DOI:10.1177/19418744231182285
Andrew Silverman, Rachelle Dugue, Paul M George
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引用次数: 0

Abstract

A 38-year-old woman with migraine headaches and systemic lupus erythematosus with recent cessation of her immunosuppressive therapy presents with prolonged headache and hypertensive emergency. Her examination is notable for a peripheral right facial palsy and stable malar rash. There are no signs of systemic infection nor systemic symptoms of a lupus flare. Initial CT head reveals bilateral hypodensities in the basal ganglia. Within 8 hours of presentation, she develops right hemiplegia and becomes encephalopathic. MRI shows multifocal acute infarcts (most notably in the left basal ganglia), enhancement of the right facial nerve, and multifocal vessel wall enhancement in the anterior and posterior circulation. We discuss the differential diagnosis, comprehensive workup, and subsequent treatment decisions in the management of this immunocompromised patient with encephalopathy, headache, and rapidly progressing focal neurologic deficits.

临床问题解决:一名患有系统性红斑狼疮的38岁女性,表现为头痛、恶心和呕吐。
一位患有偏头痛和系统性红斑狼疮的38岁女性,最近停止了免疫抑制治疗,表现为长期头痛和高血压急症。她的检查结果是周围性右面神经麻痹和稳定的马拉皮疹。没有系统性感染的迹象,也没有狼疮发作的系统性症状。初步CT头显示双侧基底节低密度。在出现症状的8小时内,她出现右侧偏瘫,并出现脑病变。MRI显示多灶性急性梗死(最明显的是左基底节),右侧面神经增强,前循环和后循环多灶性血管壁增强。我们讨论了这名患有脑病、头痛和快速发展的局灶性神经功能缺损的免疫功能低下患者的鉴别诊断、综合检查和随后的治疗决定。
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
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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