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一例罕见的新型布尼亚病毒相关噬血细胞性淋巴组织细胞增生症致死病例。

A rare fatal case of a novel bunyavirus-associated hemophagocytic lymphohistiocytosis.

作者信息

Lin Ling, Xu You-Zu, Wu Xiao-Mai, Ge Hong-Fei, Feng Jia-Xi, Chen Mei-Fang, Lv Dong-Qing, Li Bo-Li, Lin Jian

机构信息

Taizhou Hospital of Wenzhou Medical University, Linhai, China.

出版信息

J Infect Dev Ctries. 2016 May 31;10(5):533-6. doi: 10.3855/jidc.7268.

Abstract

Herein we describe a rare fatal case of a novel bunyavirus-associated hemophagocytic lymphohistiocytosis (HLH) in a 62-year-old female patient. The novel bunyavirus infects patients with or without HLH who have similar clinical features such as fever, thrombocytopenia, and leukocytopenia. Therefore, the diagnosis of HLH can be easily missed. When HLH occurs, the disease worsens and the fatality rate rises. Our finding highlights the importance of bone marrow biopsy performed as soon as possible for patients suspected of having a novel bunyavirus infection and showing marked cytopenia in three cell lines.

摘要

在此,我们描述了一例62岁女性患者罕见的新型布尼亚病毒相关噬血细胞性淋巴组织细胞增生症(HLH)致死病例。这种新型布尼亚病毒可感染患有或未患有HLH的患者,这些患者具有相似的临床特征,如发热、血小板减少和白细胞减少。因此,HLH的诊断很容易被漏诊。当HLH发生时,病情会恶化,死亡率会上升。我们的研究结果强调了对于疑似感染新型布尼亚病毒且三系血细胞明显减少的患者尽快进行骨髓活检的重要性。

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