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Hemophagocytic lymphohistiocytosis and miliary tuberculosis in a previously healthy individual: a case report
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare heterogenous genetic or acquired hyperinflammatory syndrome associated with a high degree of morbidity and mortality. HLH has clinical manifestations related to abnormal prolonged activation of T lymphocytes and macrophages with an exces...
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| Gepubliceerd in: | J Med Case Rep |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7655140/ https://ncbi.nlm.nih.gov/pubmed/33172493 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-020-02555-x |
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