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1.
Gastroenterol. hepatol. (Ed. impr.) ; 34(8): 546-550, Oct. 2011.
Artigo em Espanhol | IBECS | ID: ibc-94525

RESUMO

El tratamiento con farmacos antifactor de necrosis tumoral alfa (TNF-¦Á) en la enfermedad de Crohn es relativamente seguro aunque se han comunicado diferentes efectos secundarios cutaneos como la aparicion o exacerbacion de una psoriasis secundaria al tratamiento con anti-TNF-¦Á que, en ocasiones, puede llevar a la suspension del tratamiento. Por ello, son necesarias nuevas alternativas terapeuticas con nuevos mecanismos de accion. Se ha publicado que ustekinumab, un anticuerpo monoclonal que se une a la subunidad p40 de la interleucina 12/23, podrea inducir repuesta en pacientes con enfermedad de Crohn y ademas ha demostrado su eficacia en pacientes con psoriasis. Presentamos un caso de una paciente con enfermedad de Crohn que desarrollo psoriasis tras el tratamiento con 2 farmacos anti-TNF-¦Á (infliximab y adalimumab) que fue posteriormente tratada con ustekinumab con resolucion de las lesiones de la psoriasis y mantuvo la remision de la enfermedad de Crohn (AU)


Treatment with anti-tumor necrosis factor (TNF)-¦Á for Crohn's disease is relatively safe, although various cutaneous adverse effects have been reported such as the development or exacerbation of anti-TNF- ¦Á-induced psoriasis, which can sometimes lead to treatment withdrawal. Therefore, new alternative treatments with new mechanisms of action are required. Ustekinumab, a monoclonal antibody against the p40 subunit of interleukin 12/23, could induce response in patients with Crohn's disease and has demonstrated efficacy in patients with psoriasis. We present the case of a woman with Crohn's disease who developed psoriasis after treatment with two anti-TNF- ¦Á drugs (infliximab and adalimumab). The patient was subsequently treated with ustekinumab with resolution or psoriasis lesions and maintenance of remission of Crohn's disease (AU)


Assuntos
Humanos , Doença de Crohn/tratamento farmacológico , Psoríase/induzido quimicamente , Anticorpos Monoclonais/farmacocinética , Doença de Crohn/complicações , Fator de Necrose Tumoral alfa/antagonistas & inibidores
2.
Gastroenterol Hepatol ; 34(8): 546-50, 2011 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-21665330

RESUMO

Treatment with anti-tumor necrosis factor (TNF)-α for Crohn's disease is relatively safe, although various cutaneous adverse effects have been reported such as the development or exacerbation of anti-TNF- α-induced psoriasis, which can sometimes lead to treatment withdrawal. Therefore, new alternative treatments with new mechanisms of action are required. Ustekinumab, a monoclonal antibody against the p40 subunit of interleukin 12/23, could induce response in patients with Crohn's disease and has demonstrated efficacy in patients with psoriasis. We present the case of a woman with Crohn's disease who developed psoriasis after treatment with two anti-TNF- α drugs (infliximab and adalimumab). The patient was subsequently treated with ustekinumab with resolution or psoriasis lesions and maintenance of remission of Crohn's disease.


Assuntos
Anticorpos Monoclonais Humanizados/efeitos adversos , Anticorpos Monoclonais/efeitos adversos , Anticorpos Monoclonais/uso terapêutico , Doença de Crohn/tratamento farmacológico , Toxidermias/etiologia , Subunidade p40 da Interleucina-12/antagonistas & inibidores , Psoríase/induzido quimicamente , Fator de Necrose Tumoral alfa/antagonistas & inibidores , Adalimumab , Corticosteroides/administração & dosagem , Corticosteroides/uso terapêutico , Adulto , Anticorpos Monoclonais/administração & dosagem , Anticorpos Monoclonais Humanizados/administração & dosagem , Anticorpos Monoclonais Humanizados/uso terapêutico , Azatioprina/administração & dosagem , Azatioprina/uso terapêutico , Terapia Combinada , Quimioterapia Combinada , Feminino , Humanos , Imunossupressores/uso terapêutico , Infliximab , Subunidade p40 da Interleucina-12/imunologia , Mesalamina/administração & dosagem , Mesalamina/uso terapêutico , Fototerapia , Psoríase/tratamento farmacológico , Psoríase/terapia , Fator de Necrose Tumoral alfa/imunologia , Ustekinumab
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