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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:BMJ Case Rep
Asıl Yazarlar: Aggarwal, Puneet, Kumar, Gunjan, Dev, Nishanth, Kumari, Pushpa
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2012
Konular:
Article
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller