Adult-onset central nervous system hemophagocytic lymphohistiocytosis: a case report

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome with both genetic and acquired causes characterized by elevated cytokine levels, hyperinflammation, and overactivation of lymphocytes and macrophages. It is typically a systemic disease with variable degrees of CNS involveme...

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Dades bibliogràfiques
Publicat a:BMC Neurol
Autors principals: Pastula, Daniel M., Burish, Mark, Reis, Gerald F., Bollen, Andrew, Cha, Soonmee, Ralph, Jeffrey, Douglas, Vanja C.
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2015
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4606887/
https://ncbi.nlm.nih.gov/pubmed/26467435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-015-0470-6
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