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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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| Publicado no: | BMC Neurol |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | 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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