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An uncommon presentation of EBV-driven HLH. Primary or secondary? An ongoing dilemma
Haemophagocytic lymphohistiocytosis (HLH) is a potentially fatal syndrome, mainly characterised by dysregulated immune activation. The syndrome is related to a genetic cause, in the classic primary form, or to identified triggers such as infections, malignancy or rheumatological processes, in the cl...
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| Pubblicato in: | BMJ Case Rep |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Publishing Group
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4434350/ https://ncbi.nlm.nih.gov/pubmed/25948855 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-209615 |
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