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Fueling the FIRES : Hemophagocytic lymphohistiocytosis in febrile infection‐related epilepsy syndrome
Author(s) -
FariasMoeller Raquel,
LaFranceCorey Reghann,
Bartolini Luca,
Wells Elizabeth M.,
Baker Meredith,
Doslea Alyssa,
Suslovic William,
Greenberg Jay,
Carpenter Jessica L.,
Howe Charles L.
Publication year - 2018
Publication title -
epilepsia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.687
H-Index - 191
eISSN - 1528-1167
pISSN - 0013-9580
DOI - 10.1111/epi.14524
Subject(s) - hemophagocytic lymphohistiocytosis , epilepsy , medicine , pediatrics , intensive care medicine , psychiatry , disease
Summary Objectives Although secondary hemophagocytic lymphohistiocytosis ( HLH ) has been reported in children with critical illness of various etiologies, it has not been reported in patients with febrile infection–related epilepsy syndrome ( FIRES ). We describe a series of patients with concurrent HLH and FIRES in an effort to establish common pathophysiologic abnormalities. Methods Five patients with FIRES who were assessed for HLH were identified from a neurocritical care database. All were previously healthy and had extensive diagnostic testing. All had clinical deterioration with multiorgan dysfunction prompting HLH screening 20‐29 days after hospitalization. Markers for inflammatory dysregulation were assessed in cerebrospinal fluid ( CSF) and serum at various time points. Outcomes were assessed 6 months after presentation. Results Three patients met clinical criteria for secondary HLH . Elevation of specific cytokines/chemokines was variable. CSF neopterin, high mobility group box 1 ( HMGB 1), and C‐X‐C motif chemokine ligand 8 ( CXCL 8) were significantly elevated in all. Interleukin‐1β (IL‐1β) and IL‐18 were not elevated in any of the samples. Treatment and outcomes were variable. Significance We describe 3 patients with HLH and FIRES . The co‐occurrence of these 2 rare disorders suggests the possibility of a common immune dysregulation phenotype prolonging epileptogenesis. HLH screening in critically ill patients with FIRES may yield a broader understanding of shared inflammatory processes.