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Haemophagocytic lymphohistiocytosis in adult critical care
Haemophagocytic lymphohistiocytosis (HLH) is a syndrome of severe immune dysregulation, characterised by extreme inflammation, fever, cytopaenias and organ dysfunction. HLH can be triggered by conditions such as infection, autoimmune disease and malignancy, among others. Both a familial and a second...
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| Udgivet i: | J Intensive Care Soc |
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| Main Authors: | , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7401439/ https://ncbi.nlm.nih.gov/pubmed/32782466 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1751143719893865 |
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