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Treatment of Behçet disease by systemic infliximab Kentaro Tada 1 , Yumiko Yamamoto 1 , Koji Nishino 1 , Atsuki Fukushima 1 1Dept of Ophthalmol,Kochi Med Sch pp.1333-1336
Published Date 2009/8/15
DOI https://doi.org/10.11477/mf.1410102834
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Abstract. Purpose:To report four cases of Behçet disease treated by systemic infliximab. Cases:All were males aged 31,36,37 and 47 years respectively. All had been diagnosed with incomplete type of Behçet disease. Two cases also had neuro-Behçet disease. The frequency of acute ocular attack ranged from 1.16 to 4.6 times per year. Ocular attacks continued to recur after systemic treatment with colchicines,corticosteroid,or cyclosporine. Results:All the 4 cases had no recurrence of attacks of Behçet disease,including uveitis,after initiation of treatment with infliximab. Other therapeutic modalities,including colchicine and cyclosporine,could be discontinued. Conclusion:Systemic infliximab suppresses acute ocular attacks of refractory Behçet disease.


Copyright © 2009, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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