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Haemophagocytic syndrome with disseminated intravascular coagulation associated with tuberculosis
Haemophagocytic syndrome (HPS) is a clinical entity that combines non-specific clinical and biological features. The diagnosis is usually confirmed by a bone marrow examination. HPS may be primary or secondary to a malignancy or to an infectious or autoimmune disease. Early aggressive survey of the...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3618848/ https://ncbi.nlm.nih.gov/pubmed/23456163 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-008743 |
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