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Fulminant encephalopathy in a child with hyperferritinemic sepsis: a case report

机译:具有过热胰岛素血症的儿童的暴发性脑病:案例报告

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Sepsis-associated encephalopathy (SAE) is epidemic in intensive care units and recognized as a fatal complication of sepsis. SAE is characterized by diffuse brain dysfunction and the correct diagnosis of SAE requires ruling out direct central nervous system (CNS) infection or other types of encephalopathy, such as hepatic encephalopathy, pulmonary encephalopathy, and other encephalopathy. We reported a rare case of a 5-year-old girl who presented with abdominal pain, vomiting, recurrent seizures, and coma. Brain magnetic resonance imaging (MRI) showed diffuse white matter abnormalities in the brain on day 1. Cerebrospinal fluid (CSF) tests revealed that protein levels and glucose levels were normal without pleocytosis. CSF PCRs for pathogens were all negative. The electroencephalography examination demonstrated diffuse, generalized and slow background activity. The patient showed the symptom of hyperferritinemic sepsis with multiple organ dysfunction syndrome (MODS). SAE was also diagnosed by ruling out other encephalitis or encephalopathy. The patient made marked improvements of clinical symptoms and the lesions on brain imaging disappeared completely within two months after appropriate treatment including antibiotic treatments, methylprednisolone, intravenous immunoglobulin, membrane-based therapeutic plasma exchange (TPE), and continuous renal replacement therapy (CRRT). SAE can be a fatal complication of sepsis which asks for immediate diagnosis and treatment. Few reports have focus on MRI imaging findings on the early onset of hyperferritinemic sepsis with MODS since these children were too ill to undergo an MRI scan. However, SAE might appear before other systemic features of sepsis are obvious, and MRI could show abnormal lesion in the brain during the early course. Therefore, MRI should be performed early to diagnose this fatal complication which would play important roles in improving the clinical outcomes by early initiation with appropriate treatments.
机译:脓毒症相关的脑病(SAE)是密集护理单位的流行病,并被认为是败血症的致命并发症。 SAE的特征在于弥漫性脑功能障碍,并且SAE的正确诊断需要统治直接中枢神经系统(CNS)感染或其他类型的脑病,例如肝脑病,肺部脑病和其他脑病。我们报告了一个罕见的一个患有腹痛,呕吐,经常癫痫发作和昏迷的5岁女孩。脑磁共振成像(MRI)在第1天显示大脑中的弥漫性白质异常。脑脊液(CSF)试验显示蛋白质水平和葡萄糖水平在没有渗透性的情况下是正常的。用于病原体的CSF PCR均为阴性。脑电图检查显示弥漫性,广义和慢背景活动。患者展示了具有多个器官功能障碍综合征(MODS)的高级胰蛋白酶脓毒症的症状。通过统治其他脑炎或脑病诊断,SAE也被诊断出来。患者显着改善了临床症状的改善,脑成像的病变完全在适当的治疗后的两个月内完全消失,包括抗生素处理,甲基己酮龙,静脉内免疫球蛋白,膜系治疗血浆交换(TPE)和连续肾置换疗法(CRRT)。 SAE可以是败血症的致命并发症,要求立即诊断和治疗。很少有报道专注于MRI成像发现,早期发病了过度发霉的败血症,因为这些儿童对MRI扫描感到不安。然而,SAE可能出现在败血症的其他全身特征是显而易见的,并且MRI可以在早期课程中显示大脑中的异常病变。因此,MRI应尽早进行以诊断这种致命的并发症,该致命并发症会在通过适当治疗的早期启动改善临床结果方面发挥重要作用。

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