We report a case of a 6 year old girl with systemic onset juvenile idiopathic arthritis which presented at age of 3 years refractory to disease-modifying antirheumatic drugs and anakinra. During the first hospitalization a ganglioneuroblastoma (GNB) was diagnosed and consequently treated. During the SFOP treatment protocol for GNB our patient continued with low grade fever, but soon after the treatment the symptoms got worse, with significant rise of inflammation parameters, fever, rash and arthritis. The possibility of a GNB was immediately ruled out. During the next two years she received treatment with systemic corticosteroids, metotraxate, anakinra and thalidomide, but without any improvement or only partial with thalidomide. During this time, she also needed three times intraarticular corticosteroid treatment. We began treatment with a humanized monoclonal antibody against the interleukin-6 receptor, tocilizumab, which during the next six months resulted in almost complete remission of systemic symptoms (rash and fever), a fall in erythrocyte sedimentation rate, C-reactive protein, and ferritin serum levels, with graduate recovery in disability index and improvement of arthritis. Since her last course, she remains stable.
. 2011 Sep 14;9(Suppl 1):P204. doi: 10.1186/1546-0096-9-S1-P204
The use of tocilizumab in a child with systemic onset juvenile idiopathic arthritis and ganglioneuroblastoma
Ristic Goran
1,✉, Djokic Dragutin
1, Pasic Srdjan
1
Ristic Goran
1Department of Clinical Immunology and Pediatric Rheumatology, Department of Hematoncology, Mother and Child Health Institute of Serbia, Belgrade
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Djokic Dragutin
1Department of Clinical Immunology and Pediatric Rheumatology, Department of Hematoncology, Mother and Child Health Institute of Serbia, Belgrade
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Pasic Srdjan
1Department of Clinical Immunology and Pediatric Rheumatology, Department of Hematoncology, Mother and Child Health Institute of Serbia, Belgrade
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1Department of Clinical Immunology and Pediatric Rheumatology, Department of Hematoncology, Mother and Child Health Institute of Serbia, Belgrade
✉
Corresponding author.
Supplement
Proceedings of 18th Pediatric Rheumatology European Society (PReS) Congress
Johannes Roth, Alberto Martini, Michael Hofer, Marco Gattorno, Hermann Girschick, Pierre Quartier, Carlos Rose, Rebecca ten Cate, Rolando Cimaz, Pavla Dolezalova, Sue Maillard and Carine Wouters
Conference
14-18 September 2011
18th Pediatric Rheumatology European Society (PReS) Congress
Bruges, Belgium
Collection date 2011.
Copyright ©2011 Goran et al; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
PMCID: PMC3194563
