Hemophagocytic lymphohistiocytosis secondary to dengue in pediatric patient: case report
DOI:
https://doi.org/10.61708/q49sgq39Keywords:
Lymphohistiocytosis Hemophagocytic, dengue, paediatricsAbstract
Hemophagocytic lymphohistiocytosis (HLH) is a rare and potentially fatal condition characterized by exaggerated activation of the immune system. It can be seen in the context of several conditions such as infections, autoimmune diseases or cancer. Diagnosis requires the clinical context and compliance with the criteria proposed by the Histiocyte Society in 2004. Its management is based on the use of dexamethasone, cyclosporine A and etoposide. Here, we present the case of a 2-year-old male patient with persistent fever, signs of shock, and studies compatible with severe dengue who developed secondary HLH as a complication. The objective of this presentation is to describe a rare case in pediatrics, seeking to provide the reader with solid concepts about HLH, its management and complications.
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