Until now, systemic immunosuppressive agents, particularly oralcorticosteroids, have been the standard treatment for bullouspemphigoid, which accounts for about 75 percent of cases ofautoimmune blistering skin disease.1,2,3 Nearly two thirds ofcases occur in persons 80 years of age or older.2,3 In France,whose population is one fifth that of the United States, about500 new cases of bullous pemphigoid occur each year.2,3
Bullous pemphigoid can usually be distinguished from other blisteringskin diseases on the basis of at least three of four criteria:the absence of atrophic scars, the absence of mucosal involvement,the absence of involvement . . . [Full Text of this Article]
References
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Oral and Topical Corticosteroids in Bullous Pemphigoid
Korman N. J., Ardern-Jones M. R., Venning V. A., Wojnarowska F., Bystryn J.-C., Wainwright B. D., Shupack J. L., Spigel G. T., Joly P., Roujeau J.-C., Benichou J., Stern R. S.
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N Engl J Med 2002;
347:143-145, Jul 11, 2002.
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Korman, N. J., Ardern-Jones, M. R., Venning, V. A., Wojnarowska, F., Bystryn, J.-C., Wainwright, B. D., Shupack, J. L., Spigel, G. T., Joly, P., Roujeau, J.-C., Benichou, J., Stern, R. S.
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