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Haemophagocytic lymphohistiocytosis: a cause for rare but fatal outcome in tuberculosis
Haemophagocytic lymphohistiocytosis (HLH), also called haemophagocytic syndrome (HPS) is characterised by a dysregulated activation and proliferation of macrophages, leading to uncontrolled phagocytosis of platelets, erythrocytes, lymphocytes and their haematopoietic precursors throughout the reticu...
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| 出版年: | BMJ Case Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Group
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4544015/ https://ncbi.nlm.nih.gov/pubmed/23035171 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2012-006982 |
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