ESCOLAR DE 7 AÑOS CON FIEBRE Y HEPATOESPLENOMEGALIA, REPORTE DE CASO

A 7 YEARS OLD GIRL WITH FEVER AND HEPATOSPLENOMEGALY, A CASE REPORT

  • Consuelo Luna-Muñoz
  • Gary Carhuamaca-López
  • Rolando Vásquez-Alva
  • Erick Mattos-Villena

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

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Published
2018-01-31