Rituximab therapy for refractory systemic-onset juvenile idiopathic arthritis.

Data de publicació

2012-03-05T12:52:32Z

2012-03-05T12:52:32Z

2009

Resum

Systemic-onset juvenile idiopathic arthritis (SOJIA), formerly called Still’s disease, is a subset of juvenile arthritis that describes patients with fever, rash, arthritis, serositis and visceromegaly. In up to 30% of cases the disease has a chronic course and management requires high doses of glucocorticoids, disease-modifying antirheumatic drugs (DMARD), tumour necrosis factor alpha (TNFα) inhibitors or anakinra.1–6 However, this therapeutic arsenal is unable to control the disease in all patients.#N##N#Recently, rituximab, a chimeric anti-CD20 monoclonal antibody, has been successfully used in two patients with refractory adult-onset Still’s disease.7 As the similarity of clinical and laboratory features present in SOJIA and adult-onset Still’s disease implies that these conditions have similar …

Tipus de document

Article


Versió publicada

Llengua

Anglès

Matèries i paraules clau

Artritis; Joves; Terapèutica; Arthritis; Youth; Therapeutics

Publicat per

BMJ Group

Documents relacionats

Reproducció digital del document publicat a: http://dx.doi.org/10.1136/ard.2008.092106

Annals of the Rheumatic Diseases, 2009, vol. 68, num. 4, p. 607-608

http://dx.doi.org/10.1136/ard.2008.092106

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(c) BMJ Publishing Group Ltd, 2009

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