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Dipeptidyl‐peptidase IV inhibitor‐associated bullous pemphigoid efficiently treated with omalizumab

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Orientador(es)

Resumo(s)

Bullous pemphigoid (BP) is the most common autoimmune blistering disease. High potency topical and/or systemic corticosteroids as well as immunosuppressants are the current mainstay of treatment. However, long-term steroid therapy and systemic immunosuppression may result in significant morbidity and mortality. Contribution of IgE to BP pathogenesis remains under investigation, but increasing evidence supports a pathogenic significance. Omalizumab is a recombinant humanized monoclonal anti-IgE antibody that has recently emerged as a novel promising treatment alternative for BP.

Descrição

© 2020 Wiley Periodicals LLC.

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Contexto Educativo

Citação

Dermatol Ther. 2020 Nov;33(6):e14160

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Fascículo

Editora

John Wiley & Sons, Inc.

Licença CC

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