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Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report

BACKGROUND: Haemophagocytic lymphohistiocytosis (HLH) is an uncommon systemic inflammatory syndrome that can happen secondary to numerous conditions. It rarely occurs due to dengue infection causing significant mortality and morbidity even with appropriate treatment. The outcome is further poor if t...

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Autores principales: Pradeep, Chamila, Karunathilake, Parackrama, Abeyagunawardena, Shamali, Ralapanawa, Udaya, Jayalath, Thilak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234019/
https://www.ncbi.nlm.nih.gov/pubmed/37259116
http://dx.doi.org/10.1186/s13256-023-03967-1
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author Pradeep, Chamila
Karunathilake, Parackrama
Abeyagunawardena, Shamali
Ralapanawa, Udaya
Jayalath, Thilak
author_facet Pradeep, Chamila
Karunathilake, Parackrama
Abeyagunawardena, Shamali
Ralapanawa, Udaya
Jayalath, Thilak
author_sort Pradeep, Chamila
collection PubMed
description BACKGROUND: Haemophagocytic lymphohistiocytosis (HLH) is an uncommon systemic inflammatory syndrome that can happen secondary to numerous conditions. It rarely occurs due to dengue infection causing significant mortality and morbidity even with appropriate treatment. The outcome is further poor if the diagnosis of HLH is delayed or left untreated. Therefore, a high degree of clinical suspicion is paramount in diagnosing HLH. CASE PRESENTATION: A 17-year-old Sinhalese boy was admitted to a tertiary care hospital in Sri Lanka with a 4-day history of fever, headache, nausea, vomiting, and diarrhea. He was hemodynamically stable, and the serological investigation confirmed a dengue infection. On the fifth day of fever, he entered the critical phase of dengue infection, confirmed by ultrasound evidence of plasma leaking. However, he had ongoing high fever spikes during the critical phase, and even after the critical phase was over, the fever spikes continued. Simultaneously, hepatosplenomegaly was noticed, and he showed persistent thrombocytopenia, neutropenia, and anemia despite the resolution of the critical phase. Further, the workup revealed a serum ferritin level of > 3000 ng/mL triglyceride level of 314 mg/dL, and the bone marrow biopsy revealed an increased haemophagocytic activity. Secondary HLH was diagnosed on the basis of criteria used in the HLH-2004 trial and successfully managed with intravenous dexamethasone 10 mg/body surface area/day for the first 2 weeks, followed by a tapering regimen over 8 weeks. CONCLUSION: This case emphasizes the need to consider HLH as a potential complication when persistent fever and cytopenias are present after recovering from dengue fever, particularly in patients with unusual clinical features like hepatosplenomegaly. Early recognition and prompt treatment with appropriate immunosuppressive therapy, such as intravenous dexamethasone, can lead to a successful response and good prognosis.
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spelling pubmed-102340192023-06-02 Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report Pradeep, Chamila Karunathilake, Parackrama Abeyagunawardena, Shamali Ralapanawa, Udaya Jayalath, Thilak J Med Case Rep Case Report BACKGROUND: Haemophagocytic lymphohistiocytosis (HLH) is an uncommon systemic inflammatory syndrome that can happen secondary to numerous conditions. It rarely occurs due to dengue infection causing significant mortality and morbidity even with appropriate treatment. The outcome is further poor if the diagnosis of HLH is delayed or left untreated. Therefore, a high degree of clinical suspicion is paramount in diagnosing HLH. CASE PRESENTATION: A 17-year-old Sinhalese boy was admitted to a tertiary care hospital in Sri Lanka with a 4-day history of fever, headache, nausea, vomiting, and diarrhea. He was hemodynamically stable, and the serological investigation confirmed a dengue infection. On the fifth day of fever, he entered the critical phase of dengue infection, confirmed by ultrasound evidence of plasma leaking. However, he had ongoing high fever spikes during the critical phase, and even after the critical phase was over, the fever spikes continued. Simultaneously, hepatosplenomegaly was noticed, and he showed persistent thrombocytopenia, neutropenia, and anemia despite the resolution of the critical phase. Further, the workup revealed a serum ferritin level of > 3000 ng/mL triglyceride level of 314 mg/dL, and the bone marrow biopsy revealed an increased haemophagocytic activity. Secondary HLH was diagnosed on the basis of criteria used in the HLH-2004 trial and successfully managed with intravenous dexamethasone 10 mg/body surface area/day for the first 2 weeks, followed by a tapering regimen over 8 weeks. CONCLUSION: This case emphasizes the need to consider HLH as a potential complication when persistent fever and cytopenias are present after recovering from dengue fever, particularly in patients with unusual clinical features like hepatosplenomegaly. Early recognition and prompt treatment with appropriate immunosuppressive therapy, such as intravenous dexamethasone, can lead to a successful response and good prognosis. BioMed Central 2023-06-01 /pmc/articles/PMC10234019/ /pubmed/37259116 http://dx.doi.org/10.1186/s13256-023-03967-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Pradeep, Chamila
Karunathilake, Parackrama
Abeyagunawardena, Shamali
Ralapanawa, Udaya
Jayalath, Thilak
Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
title Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
title_full Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
title_fullStr Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
title_full_unstemmed Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
title_short Hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
title_sort hemophagocytic lymphohistiocytosis as a rare complication of dengue haemorrhagic fever: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234019/
https://www.ncbi.nlm.nih.gov/pubmed/37259116
http://dx.doi.org/10.1186/s13256-023-03967-1
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