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以不明原因发热为表现的噬血细胞性淋巴组织细胞增生症：一例病例报告及文献综述

Hemophagocytic lymphohistiocytosis presented with fever of unknown origin: A case study and literature review.

作者信息

Hakamifard Atousa, Mardani Masoud, Gholipur-Shahraki Tahereh

机构信息

Infectious Diseases and Tropical Medicine Research Center Shahid Beheshti University of Medical Sciences Tehran Iran.

Department of Infectious Diseases School of Medicine Isfahan University of Medical Sciences Isfahan Iran.

出版信息

Clin Case Rep. 2021 Mar 8;9(4):2350-2355. doi: 10.1002/ccr3.4033. eCollection 2021 Apr.

DOI:10.1002/ccr3.4033
PMID:33936693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8077318/
Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening clinical syndrome, which may present with FUO. The possible diagnosis of HLH must be considered in the differential diagnosis when a patient presents with FUO.

摘要

噬血细胞性淋巴组织细胞增生症（HLH）是一种罕见且危及生命的临床综合征，可能表现为不明原因发热（FUO）。当患者出现不明原因发热时，在鉴别诊断中必须考虑HLH的可能诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9621/8077318/677031b985ed/CCR3-9-2350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9621/8077318/677031b985ed/CCR3-9-2350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9621/8077318/677031b985ed/CCR3-9-2350-g001.jpg

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IDCases. 2020 Jun 2;21:e00861. doi: 10.1016/j.idcr.2020.e00861. eCollection 2020.
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Unusual accumulation of a wide array of antimicrobial resistance mechanisms in a patient with cytomegalovirus-associated hemophagocytic lymphohistiocytosis: a case report.患者巨细胞病毒相关性噬血细胞性淋巴组织细胞增生症中存在多种抗菌药物耐药机制的异常积聚：一例报告。
BMC Infect Dis. 2020 Mar 20;20(1):237. doi: 10.1186/s12879-020-04966-z.
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Visceral leishmaniasis presenting as haemophagocytic lymphohistiocytosis.
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BMJ Case Rep. 2019 Dec 8;12(12):e232576. doi: 10.1136/bcr-2019-232576.
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Pediatr Blood Cancer. 2019 Nov;66(11):e27929. doi: 10.1002/pbc.27929. Epub 2019 Jul 24.
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