Familial and acquired hemophagocytic lymphohistiocytosis
Clicks: 433
ID: 116748
2007
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Abstract
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening condition of severe hyperinflammation caused by the uncontrolled proliferation of activated lymphocytes and histiocytes secreting high amounts of inflammatory cytokines. Cardinal signs and symptoms are prolonged fever, hepatosplenomegaly …
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| Reference Key |
ge2007europeanfamilial
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|---|---|
| Authors | Janka GE;; |
| Journal | European journal of pediatrics |
| Year | 2007 |
| DOI |
DOI not found
|
| URL | |
| Keywords |
immunity
National Center for Biotechnology Information
NCBI
NLM
MEDLINE
review
diagnosis
humans
pubmed abstract
nih
national institutes of health
national library of medicine
risk factors
differential
lymphohistiocytosis
cytokines / metabolism
genetic predisposition to disease
cell proliferation
t-lymphocytes / metabolism
t-lymphocytes / immunology*
cellular*
pmid:17151879
doi:10.1007/s00431-006-0258-1
gritta e janka
hemophagocytic* / genetics
hemophagocytic* / immunology
hemophagocytic* / pathology
|
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