Diagnosis of Lupus Cerebritis with Balint Syndrome: A Unique Case Report

J. Cazzaniga, Cesar E Jara Silva, S. Nittala, D. Filippi
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Abstract

Introduction: Among the wide variety of clinical manifestations in Systemic Lupus Erythematosus (SLE), cognitive dysfunction (CD) is a subtle finding, where the reported prevalence ranges from 3-88% due to CD assessment inconsistencies and challenges with SLE correlations. Cognitive dysfunction may also be a cornerstone element for a diagnosis of Neuropsychiatric Systemic Lupus Erythematosus (NP-SLE). We present a case of Lupus Cerebritis displaying seizures and oculomotor dysfunctions referred to as Balint Syndrome. To our knowledge, no publications to date have shown a correlation between Lupus Cerebritis and Balint Syndrome. Case Report: A 35-year-old female with a history of lupus, seizures, and migraines presented complaining of a severe headache associated with vomiting. The patient stated the onset of her symptoms was three days prior and had been worsening. While in the emergency room, the patient had a generalized tonic-clonic seizure lasting around 2 minutes at which point neurology was consulted for seizure management. The patient had been seen about a year prior for similar complaints and was started on Keppra to control her epilepsy. The patient was seizure free for about 6 months so Keppra was discontinued. Discussion: A wide array of symptoms are associated with Lupus Cerebritis, which is a rare manifestation following a diagnosis of SLE. Our patient was having seizures and complaints of migraine with severe Balint Syndrome consisting of oculomotor apraxia, optic ataxia, and simultagnosia. Due to some patients’ rapid decline following a diagnosis of SLE and the complex diversity of symptoms, it is crucial to prevent organ failure by treating them immediately, and furthermore, to equip and educate clinicians in identifying atypical presentations. Conclusion: Due to the complexity of autoimmune diseases, patients may present with a plethora of symptomatology, ranging from mild to severe, making a thorough medical history and physical examination imperative elements of a complete workup. Since NP-SLE is a nuanced diagnosis requiring specific management, it is essential to have close follow-ups with neurology.
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狼疮性神经炎合并Balint综合征的诊断:一例独特病例报告
在系统性红斑狼疮(SLE)的各种临床表现中,认知功能障碍(CD)是一个微妙的发现,由于CD评估不一致以及与SLE相关性的挑战,报道的患病率在3-88%之间。认知功能障碍也可能是神经精神系统性红斑狼疮(NP-SLE)诊断的基础因素。我们提出一个病例狼疮脑炎表现癫痫发作和动眼肌功能障碍被称为巴林综合征。据我们所知,迄今为止没有出版物显示狼疮脑炎和巴林特综合征之间的相关性。病例报告:一名35岁女性,有狼疮、癫痫和偏头痛病史,主诉严重头痛伴呕吐。病人说她的症状是三天前开始的,并且一直在恶化。在急诊室,患者出现了持续约2分钟的全身性强直-阵挛性癫痫发作,此时向神经内科咨询癫痫发作管理。该患者大约一年前因类似的症状就诊,并开始服用凯普拉来控制癫痫。患者约6个月无癫痫发作,因此停用Keppra。讨论:狼疮性脑炎的一系列症状与狼疮性脑炎相关,这是SLE诊断后的罕见表现。我们的病人有癫痫发作和偏头痛的主诉,并伴有严重的巴林特综合征,包括动眼性失用症、视神经共济失调和拟声失认。由于一些患者在被诊断为SLE后病情迅速下降,而且症状复杂多样,因此通过立即治疗来预防器官衰竭是至关重要的,此外,还要装备和教育临床医生识别非典型症状。结论:由于自身免疫性疾病的复杂性,患者可能会出现过多的症状,从轻微到严重,因此彻底的病史和体格检查是完整检查的必要要素。由于NP-SLE是一种细微的诊断,需要特殊的治疗,因此密切的神经病学随访是必要的。
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