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Dengue-associated hemophagocyticlymphohistiocytosis in an adult A case report and literature review

Authors
Chung, Sang MiSong, Joon YoungKim, WonshikChoi, Min JooJeon, Ji HoKang, SeonghuiJung, EunjuNoh, Ji YunCheong, Hee JinKim, Woo Joo
Issue Date
2월-2017
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
corticosteroid; dengue hemorrhagic fever; severe dengue; hemophagocyticlymphohistiocytosis
Citation
MEDICINE, v.96, no.8
Indexed
SCIE
SCOPUS
Journal Title
MEDICINE
Volume
96
Number
8
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/84842
DOI
10.1097/MD.0000000000006159
ISSN
0025-7974
Abstract
Background: Infection-associated hemophagocytic syndrome (IAHS) is potentially a fatal disease caused by systemic infection complicated by hemophagocyticlymphohistiocytosis (HLH). Here, we report a case of HLH associated with dengue hemorrhagic fever (DHF) after a trip to Thailand. Case summary: A 33-year-old healthy female patient presented with 3 days of fever, myalgia, and skin rash. Serotype 3 dengue virus was isolated. Clinical and laboratory findings fulfilled the criteria of HLH. After the initiation of corticosteroid therapy, the patient recovered and laboratory findings were normalized. Conclusion: It would be important to differentially diagnose dengue-associated HLH from severe DHF. Early recognition and initiation of steroid treatment would be crucial for the successful treatment of dengue fever complicated by HLH.
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College of Medicine > Department of Medical Science > 1. Journal Articles
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