登革出血热继发脑炎和嗜血细胞淋巴组织细胞增多症:病例报告

S.D.R. Rajapaksha , S.R.M.D. Ranabahu , W.M.Y.L Wijekoon , M. Caldera , P. Rubasinghe , S.G.T. Rathnasekara , C.N. Sarathchandra , SH Siribaddana
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引用次数: 0

摘要

嗜血细胞淋巴组织细胞增多症(HLH)1 是一种致命的疾病,可能是原发性遗传病,也可能是由登革热等感染引起的继发性疾病。脑炎和脑病是登革热最常见的神经系统表现。一名 17 岁女性在登革热危重期后出现心动过速、全身僵硬、意识水平下降、抽搐和刻板动作。高烧不退,随后被诊断为铁蛋白超过 30,000 纳克/毫升的 HLH,并接受了类固醇治疗。本病例报告描述了一名在登革出血热、脑炎和 HLH 罕见组合的情况下仍存活下来的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Encephalitis & hemophagocytic lymphohistiocytosis secondary to dengue hemorrhagic fever: A case report

Hemophagocytic lymphohistiocytosis (HLH)1 is a fatal disease that may occur as a primary inherited or secondary due to several causes, including infections such as dengue. Encephalitis and encephalopathy are the most common neurological presentations of dengue. A 17-year-old female, after the critical period of dengue, developed tachycardia, rigidity, deteriorating consciousness level, seizures, and stereotyped movements. Fever did not remit and was subsequently diagnosed as HLH with ferritin more than 30,000 ng/mL and treated with steroids. This case report describes a patient who survived despite having an unusual combination of dengue hemorrhagic fever, encephalitis, and HLH.

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