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Familial haemophagocytic lymphohistiocytosis: two case reports
Haemophagocytic lymphohistiocytosis (HLH) is a life threatening inflammatory syndrome, which presents a highly stimulated but ineffective immune response with severe hypercytokinaemia. HLH, primary or secondary, is characterised by prolonged fever and hepatosplenomegaly associated with pancytopenia,...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
2010
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3047491/ https://ncbi.nlm.nih.gov/pubmed/22736603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.11.2009.2463 |
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