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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655140/ https://www.ncbi.nlm.nih.gov/pubmed/33172493 http://dx.doi.org/10.1186/s13256-020-02555-x |