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Hemophagocytic lymphohistiocytosis as a diagnostic consideration of fever of unknown origin with pancytopenia and chronic liver disease

Hemophagocytic lymphohistiocytosis (HLH) is a severe disorder of systemic immune dysregulation which can be primary or secondary to autoimmune disorders, malignancy, or infections. We hereby describe a case of a 23-year-old male with severe hepatitis along with pancytopenia and prolonged fever of un...

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Detalhes bibliográficos
Publicado no:J Family Med Prim Care
Main Authors: Amisha, Malik, Paras, Pathania, Monika, Rathaur, Vyas K., Kaeley, Nidhi
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6510086/
https://ncbi.nlm.nih.gov/pubmed/31143751
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jfmpc.jfmpc_190_19
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