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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Detalles Bibliográficos
Autores principales: Amisha, Malik, Paras, Pathania, Monika, Rathaur, Vyas K., Kaeley, Nidhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510086/
https://www.ncbi.nlm.nih.gov/pubmed/31143751
http://dx.doi.org/10.4103/jfmpc.jfmpc_190_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510086/
https://www.ncbi.nlm.nih.gov/pubmed/31143751
http://dx.doi.org/10.4103/jfmpc.jfmpc_190_19

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