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Systemic infliximab was effective in a case of Behçet disease Kentaro Kurata 1 , Tatsuhiko Asai 1 , Kenro Koide 1 , Ryo Asaoka 1 , Noriyoshi Ogawa 2 , Hiroyuki Ohashi 2 , Yoshihiro Hotta 1 1Dept of Ophthalmol,Hamamatsu Univ Sch of Med 2Dept of Immunol,Hamamatsu Univ Sch of Med pp.973-979
Published Date 2009/6/15
DOI https://doi.org/10.11477/mf.1410102762
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Abstract. Purpose:To report a case of Behçet disease that responded to systemic infliximab. Case:A 55-year-old male presented with blurring in both eyes since 2 months before. He had had repeated episodes of aphthous stomatitis,and had skin lesions and genital ulcer since one year before. Topical and peroral corticosteroid proved futile. Findings and Clinical Course:Corrected visual acuity was 0.3 right and 0.2 left. Both eyes showed iritis,vitreous opacity and retinal vasculitis. He was diagnosed with complete type of Behçet disease. Topical corticosteroid and peroral colchicine failed to prevent further ocular attacks. He started receiving infliximab 15 months after his initial visit. Manifestations of the disease gradually subsided. He is doing well with no ocular attacks,aphthous stomatitis,skin eruptions nor genital ulcer at present after 38 months of treatment. Conclusion:Behçet disease may be brought to remission by administration of infliximab.


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

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