Difference between revisions of "Hemophagocytic syndrome"
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#Primary, i.e. inherited. | #Primary, i.e. inherited. | ||
#Secondary: | #Secondary: | ||
#*Infection, e.g. EBV, HIV. | #*Infection, e.g. [[EBV]], [[HIV]]. | ||
#*Malignancy. | #*Malignancy. | ||
#*Rheumatologic condition. | #*Rheumatologic condition. | ||
Revision as of 03:40, 20 September 2010
Hemophagocytic syndrome, also known as hemophagocytic lymphohistiocytosis, is a rare condition often associated with viral infections.
Clinical
Features:[1]
- Fever.
- Splenomegaly.
- Jaundice.
Classification
Classified by etiology:[2]
Microscopic
Features:[1]
- Macrophages with phagocytosed:
- Erythrocytes.
- Leukocytes.
- Platelets.
Image(s): HLH (WC).
See also
References
- ↑ 1.0 1.1 Fisman DN (2000). "Hemophagocytic syndromes and infection". Emerging Infect. Dis. 6 (6): 601–8. PMC 2640913. PMID 11076718. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640913/?tool=pubmed.
- ↑ Gupta S, Weitzman S (January 2010). "Primary and secondary hemophagocytic lymphohistiocytosis: clinical features, pathogenesis and therapy". Expert Rev Clin Immunol 6 (1): 137–54. PMID 20383897.