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Editorial
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Volume 346:364-367 January 31, 2002 Number 5
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Bullous Pemphigoid Therapy — Think Globally, Act Locally

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 by Joly, P.
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Until now, systemic immunosuppressive agents, particularly oral corticosteroids, have been the standard treatment for bullous pemphigoid, which accounts for about 75 percent of cases of autoimmune blistering skin disease.1,2,3 Nearly two thirds of cases occur in persons 80 years of age or older.2,3 In France, whose population is one fifth that of the United States, about 500 new cases of bullous pemphigoid occur each year.2,3

Bullous pemphigoid can usually be distinguished from other blistering skin 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


Related Letters:

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. Correspondence

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