Dengue-Induced Hemophagocytic Lymphohistiocytosis: A Case Report and Literature Review

被引:10
作者
Munshi, Adeeb [1 ]
Alsuraihi, Anas [2 ]
Balubaid, Marwan [3 ]
Althobaiti, Mohammad [2 ]
Althaqafi, Abdulhakeem [4 ]
机构
[1] King Saud bin Abdulaziz Univ Hlth Sci, King Abdullah Int Med Res Ctr, Minist Natl Guard Hlth Affairs, Coll Med,Infect Dis, Jeddah, Saudi Arabia
[2] King Saud bin Abdulaziz Univ Hlth Sci, King Abdullah Int Med Res Ctr, Minist Natl Guard Hlth Affairs, Coll Med,Adult Hematol, Jeddah, Saudi Arabia
[3] King Saud bin Abdulaziz Univ Hlth Sci, King Abdullah Int Med Res Ctr, Minist Natl Guard Hlth Affairs, Coll Med,Internal Med, Jeddah, Saudi Arabia
[4] King Saud Bin Abdulaziz Univ Hlth Sci, King Abdullah Int Med Res Ctr, King Abdulaziz Med City, Infect Dis, Jeddah, Saudi Arabia
关键词
cytopenia; hepatomegaly; hyperferritinemia; dengue fever; hemophagocytic lymphohistiocytosis; ETOPOSIDE; DISEASE; HLH;
D O I
10.7759/cureus.20172
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hemophagocytic lymphohistiocytosis (HLH) is an uncommon fatal disease of otherwise normal but hyperactive lymphocytes and histocytes. HLH could be primary (hereditary) or secondary (acquired). Fever, hepatosplenomegaly, lymphadenopathy, and neurologic dysfunction are among the common symptoms of HLH. The diagnosis of HLH is based on clinical and biochemical findings. We report here a case of a patient infected with the dengue virus who developed HLH during hospitalization. A 63-year-old female known case of asthma on inhalers, chronic hepatitis B virus, gastritis on proton pump inhibitors, and hemoglobin H disease presented to the emergency department (ED) with a history of high-grade fever (highest recorded temperature 40 degrees C/104 degrees F), which was relieved partially by antipyretics, generalized fatigability, body aches, headache and mosquito bites for four days. The physical examination was significant for hepatomegaly of 4 cm below the right costal margin. Investigations revealed pancytopenia with elevated ferritin levels (> 40000 mu g/L). Viral serology was positive for dengue NS1 antigen. After hematology consultation, a bone marrow biopsy was done, which showed trilineage hematopoiesis with increased histiocytes and occasional hemophagocytosis. Given that the patient was clinically stable and there was a clear triggering condition, we opted for supportive measures rather than HLH-specific therapy. The patient was given 2 units packed red blood cells for anemia. On the following days, the patient has no recurrence of fever, with marked improvement in the biochemical profile including ferritin level (1165 mu g/L). HLH is a deleterious disease with a high fatality rate, which requires the clinician to have a low threshold for suspicion in the differentials of children and adults with symptoms of persistent fever, hepatosplenomegaly, and cytopenia. Dengueassociated HLH diagnosis is challenging, but it is very important to be recognized, as early recognition is associated with better outcomes. Physicians must work in collaboration with pathologists and microbiologists for the proper diagnosis.
引用
收藏
页数:6
相关论文
共 50 条
  • [31] Hemophagocytic lymphohistiocytosis (HLH): a review of literature
    Rohtesh S. Mehta
    Roy E. Smith
    Medical Oncology, 2013, 30
  • [32] Hemophagocytic lymphohistiocytosis (HLH): a review of literature
    Mehta, Rohtesh S.
    Smith, Roy E.
    MEDICAL ONCOLOGY, 2013, 30 (04)
  • [33] Hemophagocytic Lymphohistiocytosis Induced by Brucellosis: A Case Report
    Park, Daniel
    Yoon, Kevin
    Lo, Amanda
    Bolos, David
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (07)
  • [34] Hemophagocytic lymphohistiocytosis and visceral leishmaniasis in children: case report and systematic review of literature
    Scalzone, Maria
    Ruggiero, Antonio
    Mastrangelo, Stefano
    Trombatore, Giovanna
    Ridola, Vita
    Maurizi, Palma
    Riccardi, Riccardo
    JOURNAL OF INFECTION IN DEVELOPING COUNTRIES, 2016, 10 (01): : 103 - 108
  • [35] Acute HIV infection presenting as hemophagocytic lymphohistiocytosis: case report and review of the literature
    Farheen Manji
    Evan Wilson
    Etienne Mahe
    John Gill
    John Conly
    BMC Infectious Diseases, 17
  • [36] Hemophagocytic lymphohistiocytosis: An unusual presentation of disseminated tuberculosis: A case report and literature review
    Poornachandra
    Wotiye, Abdi Bati
    Ayele, Biniyam A.
    JOURNAL OF CLINICAL TUBERCULOSIS AND OTHER MYCOBACTERIAL DISEASES, 2022, 27
  • [37] Secondary hemophagocytic lymphohistiocytosis associated with heat stroke: A case report and review of literature
    Wi, Wongook
    Yoon, Kyoung Won
    Kim, Hyo Jin
    MEDICINE, 2023, 102 (21) : E33842
  • [38] A case of hemophagocytic lymphohistiocytosis with a significant response to baricitinib: a first report with review of literature
    Kensuke Irino
    Fumiaki Jinnouchi
    Shota Nakano
    Takuya Sawabe
    Clinical Rheumatology, 2023, 42 : 1959 - 1963
  • [39] A Case Report of Immune Checkpoint-Related Hemophagocytic Lymphohistiocytosis and Review of the Literature
    Herman, Michael
    Lee, Andrea
    Fawcett, Sandra
    Deodhare, Sanjeev
    CASE REPORTS IN ONCOLOGY, 2024, 17 (01): : 809 - 817
  • [40] Hemophagocytic Lymphohistiocytosis Associated With Hemolytic Uremic Syndrome in a Child: A Case Report and Systematic Literature Review
    Tas, Nesrin
    Gokceoglu, Arife U.
    Yayla, Burcu C. C.
    Ozcan, Aysegul
    Sac, Rukiye U.
    Vezir, Emine
    Alioglu, Bulent
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2022, 44 (05) : E905 - E910