Acta Medica
Hemophagocytic Lymphohistiocytosis: an update to diagnosis and management
Yazarlar: ule Ünal
Cilt 45 , Sayı 1 , 2014 , Sayfalar -
Konular:-
Anahtar Kelimeler: Hemophagocytic lymphohistiocytosis,HLH,Perforin
Özet: Hemophagocytic lymphohistiocytosis (HLH) is the uncontrolled reaction of the immune system against a triggering pathogen and inability of the im- mune system to elliminate this triggering factor, which ends up with hyper- cytokinemia and hemophagocytosis. Hemophagocytic lymphohistiocytosis is classified into two major groups as genetic (primary) and acquired (sec- ondary). The condition has high mortality rates and specific tratment is re- quired in most of the cases
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BibTex
KOPYALA
@article{2014, title={Hemophagocytic Lymphohistiocytosis: an update to diagnosis and management}, volume={45}, publisher={Acta Medica}, author={Sule Ünal, [MD]}, year={2014} }
APA
KOPYALA
Sule Ünal, [MD]. (2014). Hemophagocytic Lymphohistiocytosis: an update to diagnosis and management (Vol. 45). Vol. 45. Acta Medica.
MLA
KOPYALA
Sule Ünal, [MD]. Hemophagocytic Lymphohistiocytosis: An Update to Diagnosis and Management. no., Acta Medica, 2014.