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Rheumatology 2003; 42: 800-802
© 2003 British Society for Rheumatology


Letters to the Editor

Haemophagocytic syndrome in a rheumatoid arthritis patient treated with infliximab

A. Aouba1,3,, M. De Bandt1, E. Aslangul1, N. Atkhen2 and B. Patri1

1 Department of Internal Medicine and Rheumatology and
2 Unit of Haematology, Hôpital Européen Georges Pompidou and
3 Department of Haematology, Hôpital Necker-Enfants Malades, Paris, France

The first 10% of the full text of this article appears below.

SIR, Inhibitors of tumour necrosis factor {alpha} (TNF-{alpha}; monoclonal antibodies or soluble receptors) have proven their efficacy in the treatment of rheumatoid arthritis (RA) and are currently under investigation in other chronic inflammatory diseases. However, an increase in infectious complications is noticed with these molecules. We report an RA patient who developed haemophagocytic syndrome (HPS) while she was being treated with infliximab.

A 46-yr-old woman had suffered from seropositive RA (American Rheumatism Association criteria) since 1999. Despite active treatment with steroids, methotrexate and sulphasalazine, the disease remained active [disease activity score (DAS) >4.5]. Treatment with infliximab (3 mg/kg) was started in December 2000 with a good . . . [Full Text of this Article]


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