SARS-CoV-2引发的嗜血细胞淋巴组织细胞增多症并发后可逆性脑病综合征

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2024-07-30 eCollection Date: 2024-01-01 DOI:10.1155/2024/8829060
Ross M Perry, Scott D Casey, Alex Q Lee, Sylvia P Bowditch, Mary A Rasmussen, Viyeka Sethi, Arun R Panigrahi
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摘要

本文描述了一例新型 SARS-CoV-2 相关性嗜血细胞淋巴组织细胞增多症(HLH)并发后可逆性脑病综合征(PRES)的病例。患者最初被诊断为儿童多系统炎症反应(MIS-C),在出现神经系统症状前几天接受了大剂量皮质类固醇治疗。在出现 PRES 后,患者接受了降压药、抗癫痫药、地塞米松和阿纳金雷的治疗,最终神经功能恢复正常。我们建议,鉴于 HLH 或 MIS-C 患者出现 PRES 的诊断情况极具挑战性,在皮质类固醇诱导期间对血压进行制度化管理可能会显著改善因高炎症综合征接受治疗并出现神经症状的患者的预后。
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SARS-CoV-2-Triggered Hemophagocytic Lymphohistiocytosis with Complications of Posterior Reversible Encephalopathy Syndrome.

In this article, we describe a novel case of SARS-CoV-2-associated-hemophagocytic lymphohistiocytosis (HLH) complicated by posterior reversible encephalopathy syndrome (PRES). Initially diagnosed with multisystem inflammatory response in children (MIS-C), the patient received a large corticosteroid dose days before the onset of neurological symptoms. After developing PRES, the patient was treated with antihypertensives, antiepileptics, dexamethasone, and anakinra, leading to neurologic normalization. We propose that given the challenging diagnostic picture of PRES developing in patients with HLH or MIS-C, institutionalized standards for blood pressure management during corticosteroid induction may significantly improve outcomes in patients being treated for hyperinflammatory syndromes who develop neurological symptoms.

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自引率
11.10%
发文量
48
审稿时长
13 weeks
期刊最新文献
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