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. 2016:2016:1467583.
doi: 10.1155/2016/1467583. Epub 2016 Mar 13.

Successful Discontinuation of Infliximab in a Refractory Case of Vasculo-Behçet Disease

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Successful Discontinuation of Infliximab in a Refractory Case of Vasculo-Behçet Disease

Akihiro Nakamura et al. Case Rep Rheumatol. 2016.

Abstract

Reports have shown that antitumor necrosis factor alpha (anti-TNF-α) agents including infliximab (IFX) can dramatically suppress the disease activity of refractory vasculo-Behçet disease (vasculo-BD). However, it is completely unknown whether we can discontinue anti-TNF-α agents under clinical remission. A 31-year-old patient with vasculo-BD was initially treated with a high dose of steroid and intravenous cyclophosphamide therapy. Six months later, however, the disease recurred. IFX was administered and immediately the disease activity was reduced. Fortunately, we could discontinue IFX after 18-month remission and no recurrence has been observed. Based on previous reports and our patient, all patients who could discontinue IFX sustained clinical remission for at least one year, continued taking immunosuppressive agents such as methotrexate and azathioprine, and had vascular involvements only in non-life-threatening major vessels such as leg or arm arteries/veins. This is a report suggesting the possibility of discontinuation of IFX in vasculo-BD.

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Figures

Figure 1
Figure 1
Clinical manifestations on admission. Physical examination identified swollen left upper arm (a), erythema nodosum on the left forearm (b), and purpura on the left wrist joint (c), suggesting a deficiency of blood supply on the left arm.
Figure 2
Figure 2
Computed Tomography Angiography showed severe stenosis of left brachial (a) and radial (c) arteries before infliximab (IFX) induction. After IFX therapy, the artery stenosis was immediately resolved and sustained clinical remission ((b) and (d) at 12 months since IFX was introduced).
Figure 3
Figure 3
Patient's clinical time course. mPSL methylprednisolone, PSL prednisolone, IVCY intravenous cyclophosphamide, and MTX methotrexate.

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