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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Vydáno v:J Med Case Rep
Hlavní autoři: Trovik, Linn Hereide, Sandnes, Miriam, Blomberg, Bjørn, Holmaas, Gunhild, Ahmed, Aymen Bushra, Tvedt, Tor Henrik Anderson, Vintermyr, Olav, Reikvam, Håkon
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2020
Témata:
Case Report
On-line přístup: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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