Case Report: Refractory macrophage activation syndrome requiring high-dose anakinra, emapalumab, and etoposide therapy in early-onset systemic juvenile idiopathic arthritis associated with adenoviremia
Macrophage activation syndrome (MAS) is a life-threatening condition characterized by the excessive stimulation of macrophages and T lymphocytes, provoked by infections, malignancy, and autoimmune or autoinflammatory conditions such as systemic juvenile idiopathic arthritis (sJIA). Clinical signs of...
Saved in:
Main Authors: | Elizabeth D. Slaney (Author), Renee Modica (Author), Leandra Woolnough (Author), Dina Kafisheh (Author), Denise Heather Bell-Brunson (Author), Melissa Elder (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2024-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Case Report: Hypocomplementemic urticarial vasculitis syndrome in a pediatric patient with complement factor 1 deficiency
by: Sallie Lin, et al.
Published: (2024) -
Case Report: Successful avoidance of etoposide for primary hemophagocytic lymphohistiocytosis-induced multiple organ dysfunction syndrome using emapalumab
by: Timothy J. Hahn, et al.
Published: (2024) -
BK viruria and viremia in children with systemic lupus erythematosus
by: Nirupama Gupta, et al.
Published: (2017) -
The relationships of kinesiophobia and physical function and physical activity level in juvenile idiopathic arthritis
by: Leandra U. Woolnough, et al.
Published: (2022) -
Schnitzler syndrome refractory to anakinra: successful treatment with canakinumab
by: Angel Luis Salcedo-Mingoarranz, et al.
Published: (2023)