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- W2895547078 abstract "Hemophagocytic lymphohistiocytosis HLH is a fatal but distinct disease in which uncontrolled activation of immune system occurs It is characterized by fever pancytopenia splenomegaly and hemophagocytosis in bone marrow liver or lymph nodes It has been associated with viral bacterial fungal and parasitic infection Although an early diagnosis and treatment is the key to decrease the mortality but it is difficult to diagnose this case as it involves numerous laboratory tests which are non specific We report a case of EBV infection induced hemophagocytic lymphohistiocytosis in a year old male child presenting with prolonged fever pancytopenia hepatosplenomegaly multiple lymphadenopathies apthous ulcer and skin rashes This case highlights that awareness of this entity high index of suspicion and team work between clinician and pathologist can help in early diagnosis and treatment of the patients thereby decreasing the mortality rate" @default.
- W2895547078 created "2018-10-12" @default.
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- W2895547078 date "2018-10-04" @default.
- W2895547078 modified "2023-09-28" @default.
- W2895547078 title "A case report of hemophagocytic lymphohistiocytosis (HLH) in a child mimicking tuberculosis" @default.
- W2895547078 doi "https://doi.org/10.15406/acp.2018.03.00063" @default.
- W2895547078 hasPublicationYear "2018" @default.
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