Life threatening pericardial and neurologic presentations in systemic lupus erythematosus

Linle Hou, Seung Eun Lee, F. DeMichele, B. Osorio, N. Nagella
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引用次数: 1

Abstract

Background: Posterior reversible encephalopathy syndrome (PRES) is characterized by altered mental status, visual perception abnormalities and seizures. Systemic lupus erythematosus (SLE) is a rare etiology of PRES and affects less than 1% of SLE patients. We present a unique case of a new-onset SLE patient presenting with borderline cardiac tamponade requiring emergent pericardiocentesis and hospital course complicated by intractable seizures found to have PRES on imaging.Case presentation: A 21-year-old female underwent outpatient evaluation for new-onset SLE presenting to the emergency room with dyspnea. She was found to have a large circumferential pericardial effusion with borderline tamponade features requiring emergent pericardiocentesis. On her fifth hospital day, she developed generalized motor seizure (tonic-clonic) with magnetic resonance imaging (MRI) revealing bilateral parieto-occipital edema consistent with a radiographic diagnosis of PRES. Induction therapy with mycophenolate was started and follow-up studies showed improvement in the cortical and subcortical regions on MRI with no evidence of recurrent pericardial effusion.Conclusions: PRES is a rare complication of lupus and has been infrequently described in literature. It is thought that the association is secondary to the effect of SLE on endothelial dysfunction and the effect of cytotoxic medication on the loss of autoregulation of systemic hypertension. It is important to recognize this condition and its significant associations as early detection and intervention often lead to favorable outcomes. To our knowledge, this is the first case report of SLE with associations of both PRES and circumferential pericardial effusion with tamponade physiology, both of which are rare in the SLE patient population.
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系统性红斑狼疮的危及生命的心包和神经系统表现
背景:后部可逆性脑病综合征(PRES)以精神状态改变、视觉感知异常和癫痫发作为特征。系统性红斑狼疮(SLE)是一种罕见的PRES病因,影响不到1%的SLE患者。我们报告一个独特的病例,新发SLE患者表现为交界性心包填塞,需要紧急心包穿刺,住院期间并发难治性癫痫发作,影像学上发现有PRES。病例介绍:一名21岁女性因新发系统性红斑狼疮接受门诊评估,并因呼吸困难进入急诊室。她被发现有大量的周围性心包积液并伴有交界性心包填塞特征,需要紧急心包穿刺。住院第五天,患者出现全面性运动性癫痫(强直-阵挛),磁共振成像(MRI)显示双侧顶枕水肿,符合PRES的影像学诊断。开始使用麦考酚酸盐诱导治疗,随访研究显示MRI显示皮质和皮质下区域改善,无复发心包积液的证据。结论:PRES是一种罕见的狼疮并发症,在文献中很少有报道。据认为,这种关联是继发于SLE对内皮功能障碍的影响和细胞毒性药物对全身性高血压自我调节丧失的影响。认识到这种情况及其显著相关性是很重要的,因为早期发现和干预往往会导致良好的结果。据我们所知,这是第一例SLE同时伴有PRES和周围心包积液与心包填塞生理相关的病例报告,这两种情况在SLE患者群体中都很少见。
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