Escolar de 7 años con fiebre y hepatoesplenomegalia, reporte de caso

A 7 years old girl with fever and hepatosplenomegaly, a case report

Abstract

Abstract

Hemophagocytic lymphohistiocytosis (HLH), is rare, is caused by a dysfunction of cellular immunity by an alteration of NK cells (primary) or by an excessive proliferation of activated (secondary) macrophages. It is characterized by fever, hepatosplenomegaly, cytopenia, hemophagocytosis, hypertriglyceridemia and / or hypofibrinogenemia. In conclusion, in the presence of fever, hepatosplenomegaly and cytopenia, the diagnosis of hemophagocytic lymphohistiocytosis (HLH) should be considered.

Key words: Fever; Hepatosplenomegaly; Cytopenia. (source: MeSH NLM)

DOI: https://doi.org/10.25176/RFMH.v18.n1.1274