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Pentoxifylline Use for Behçet’s Disease

The result of a survey among rheumatologists in North America

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Adamantiades-Behçet’s Disease

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 528))

Conclusions

Behçet’s disease was infrequently encountered in North America, 1.7 cases per rheumatologist, with female to male ratio of 2,5/1. As previously reported2,3, pentoxifylline was useful in alleviating 50% of oral ulcers and 39% of genital ulcers of Behçet’s patients in North America, at least partially. In conjunction with colchicine, the efficacy significatly improved to 45% for oral ulcers and 48% for genital ulcers (P < 0.001). Pentoxifylline and/or colchicine appeared to have limited efficacy for the other manifestations of Behçet’s disease. Pentoxifilline and/or colchicine was under-utilished by rheumatologists who had patients with Behçet’s disease.

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References

  1. Washba-Yahav A., 1995, Pentoxifylline in intractable recurrent aphthous stomatitis: An open trial. J. Am. Acad. Dermatol. 33: 680–682.

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  2. Yasui, K., Ohta, K., Kobayashi, M., et al., 1996, Successful treatment of Behçet’s disease with pentoxifylline. Ann. Intern. Med. 124: 891–893.

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  3. Chang, E.M., and Liang, G.C., 2000, Pentoxifylline use for Behçet’s disease. Arthritis Rheum. 43: S363.

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© 2004 Kluwer Academic Publishers

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Liang, G.C., Chang, E.M. (2004). Pentoxifylline Use for Behçet’s Disease. In: Zouboulis, C.C. (eds) Adamantiades-Behçet’s Disease. Advances in Experimental Medicine and Biology, vol 528. Springer, Boston, MA. https://doi.org/10.1007/0-306-48382-3_120

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  • DOI: https://doi.org/10.1007/0-306-48382-3_120

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-306-47757-7

  • Online ISBN: 978-0-306-48382-0

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