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Difference between revisions of "Hemophagocytic syndrome"
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| Line 11: | Line 11: | ||
| IHC = | | IHC = | ||
| EM = | | EM = | ||
| Molecular = | | Molecular = primary form: FHL1 mutation or FHL2 mutation; autosomal recessive | ||
| IF = | | IF = | ||
| Gross = | | Gross = | ||
| Grossing = | | Grossing = | ||
| Site = [[lymph nodes]], [[liver]], [[spleen]], [[bone marrow]], others | | Site = [[lymph nodes]], [[liver]], [[spleen]], [[bone marrow]], others | ||
| Assdx = only in ''secondary'' (EBV infection, malignancy, rheumatologic disease) | | Assdx = only in ''secondary'' form (EBV infection, malignancy, rheumatologic disease) | ||
| Syndromes = | | Syndromes = | ||
| Clinicalhx = +/-consanguinity for ''primary'' | | Clinicalhx = +/-consanguinity for ''primary'' form | ||
| Signs = fever, [[splenomegaly]], jaundice | | Signs = fever, [[splenomegaly]], jaundice | ||
| Symptoms = | | Symptoms = | ||