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DOI 10.1016/j.medcli.2024.09.004

Медицинская библиотека · Medicina clinica · 2024

Dermatoses in patients with inflammatory bowel disease under tumor necrosis factor-alpha inhibitors treatment.

Magalhães Carolina Mundim Couto, Bartholo Marina Ribeiro, Correa Bernardo Henrique Mendes, Ferrari Maria de Lourdes Abreu, Ferrari Teresa Cristina Abreu

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Аннотация

INTRODUCTION

Tumor necrosis factor-alpha inhibitor (anti-TNF-α) agents are essential in treating inflammatory bowel diseases (IBD). Their use, however, may cause dermatoses. This study aims to characterize the dermatoses in IBD patients on anti-TNF-α therapy.

METHODS

A total of 175 IBD patients, 105 (60%) on anti-TNF-α therapy were consecutively selected in a Brazilian referral center of gastroenterology and were evaluated by a dermatologist, regardless of whether they had dermatological complaints.

RESULTS

The most prevalent disorders in patients receiving anti-TNF-α were skin infections (52.4%), unspecified alopecia not associated with psoriasiform eruptions (32.4%), seborrheic dermatitis (27.6%), infusion/injection reactions (14.5%), and psoriasiform eruptions (11.4%). The group not on anti-TNF-α treatment also presented a high prevalence of infection, seborrheic dermatitis, and alopecia, but no psoriasiform eruptions. There was a higher prevalence of dermatoses, when considered together, in patients taking anti-TNF-α. The use of these agents was independently associated with presence of dermatoses when grouped.

CONCLUSION

The prevalence of dermatoses, considering together, was higher in the anti-TNF-α group. Infections, alopecia, seborrheic dermatitis, administration reactions, and psoriasiform eruptions were the most frequent dermatoses in patients taking anti-TNF-α.

Для цитирования: Magalhães Carolina Mundim Couto, Bartholo Marina Ribeiro, Correa Bernardo Henrique Mendes, Ferrari Maria de Lourdes Abreu, Ferrari Teresa Cristina Abreu. Dermatoses in patients with inflammatory bowel disease under tumor necrosis factor-alpha inhibitors treatment.. Medicina clinica. 2024. DOI: 10.1016/j.medcli.2024.09.004.

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