Affiliations 

  • 1 Hospital Pakar Sultanah Fatimah, Medical Department, Muar, Johor, Malaysia. soonliang13@hotmail.com
  • 2 Hospital Pakar Sultanah Fatimah, Medical Department, Muar, Johor, Malaysia
  • 3 Hospital Sultanah Aminah, Internal Medicine (Infectious Diseases), Johor Bahru, Johor, Malaysia
Med J Malaysia, 2017 02;72(1):62-64.
PMID: 28255145

Abstract

Haemophagocytic lymphohistiocytosis (HLH) is a potentially fatal disorder resulting from uncontrolled hyperinflammatory response. There had been increase in cases of one of the secondary form of HLH, i.e., infectionassociated haemophagocytic syndrome (IAHS) in severe dengue in recent years. However, the condition remains under diagnosed due to lack of awareness compounded by the lack of validated diagnostic criteria. Severe hepatitis with prolonged cytopenias, severe hyperferritinemia, hypofibrinogenemia and persistent fever were evident in all four cases reported. All the subjects survived with supportive care and adjuvant steroid therapy. Prospective controlled studies are needed to develop diagnostic criteria and management protocol for IAHS in severe dengue.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.