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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Detaylı Bibliyografya
Asıl Yazarlar: Cherif, Eya, Bel Feki, Nabil, Ben Hassine, Lamia, Khalfallah, Narjess
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 2013
Konular:
Article
Online Erişim: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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