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A Case of Macropharge Activation Syndrome Successfully Treated with Combination Therapy Including Etanercept
Author(s) -
Young Seok Sim,
Hyun Soo Kim,
Kwang Nam Kim
Publication year - 2012
Publication title -
journal of rheumatic diseases
Language(s) - English
Resource type - Journals
eISSN - 2093-940X
pISSN - 2233-4718
DOI - 10.4078/jrd.2012.19.4.225
Subject(s) - etanercept , macrophage activation syndrome , medicine , pancytopenia , coagulopathy , methylprednisolone , infliximab , tumor necrosis factor alpha , rheumatoid arthritis , juvenile rheumatoid arthritis , combination therapy , immunology , arthritis , cytokine , gastroenterology , bone marrow
Macrophage activation syndrome (MAS) is a severe, potentially life-threatening complication of childhood systemic inflammatory disorder, primarily systemic onset juvenile rheumatoid arthritis (SoJRA). It is characterized by pancytopenia, liver insufficiency, coagulopathy, and neurologic symptoms. The clinical manifestations are caused by the activation and uncontrolled proliferation of T lymphocytes and macrophages, leading to cytokine overproduction including tumor necrosis factor-α (TNF-α). Methylprednisolone pulse therapy and cyclosporine A have made a considerable progress in the treatment of MAS. However, the mortality rate remains high suggesting the need of another therapeutic agent. Several cases of MAS successfully treated with TNF-α inhibitor (etanercept) have been reported. We report the first Korean case of MAS successfully treated with combination therapy of corticosteroid, cyclosporine A and etanercept.

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