Role of plasma exchange, leukocytapheresis, and plasma diafiltration in management of refractory macrophage activation syndrome.
Noriko KinjoKazuya HamadaChika HirayamaMasaki ShimizuPublished in: Journal of clinical apheresis (2017)
Macrophage activation syndrome (MAS) is a life-threating complication of systemic juvenile idiopathic arthritis (s-JIA). Steroid and cyclosporine (CsA) are effective for MAS, but, treatment for steroid- and CsA-resistant patients is still challenging. We report the case of steroid and CsA resistant s-JIA associated MAS misdiagnosed as Kawasaki disease (KD), who was successfully treated with the combination of plasma exchange (PE) and leukocytapheresis (LCAP) followed by plasma diafiltration (PDF). PE + LCAP effectively removed proinflammatory cytokines and reduced the number of peripheral white blood cells. Furthermore, PDF also removed proinflammatory cytokines as effectively as PE + LCAP. Early diagnosis of s-JIA is necessary to avoid developing MAS. The measurement of serum ferritin and IL-18 levels are useful for differentiating s-JIA from KD. Apheresis therapies are an alternative option to induce remission for severe patients with steroid- or CsA-resistant MAS.
Keyphrases
- juvenile idiopathic arthritis
- disease activity
- end stage renal disease
- adipose tissue
- ejection fraction
- chronic kidney disease
- induced apoptosis
- rheumatoid arthritis
- case report
- newly diagnosed
- systemic lupus erythematosus
- magnetic resonance imaging
- oxidative stress
- cell death
- magnetic resonance
- cell proliferation
- patient reported outcomes
- ulcerative colitis