Psoriatic eruption following immunotherapy with pembrolizumab: a case report

Psoriatic eruption following immunotherapy with pembrolizumab: a case report

Tânia R.M. de Oliveira-Fernandes 1 , Carlos E. Lopes-Pires 1 , Mariana R. Brandão-Braga 1 , Raquel J. Campos-e-Nonato 1 , Davi M. Moreira-Antunes 1

1 Department of Medicine, Federal University of Vale do São Francisco – Main Campus, Avenida José de Sá Maniçoba, s/n, Centro District, Petrolina, Pernambuco, Brazil

Tânia R.M. de Oliveira-Fernandes, Carlos E. Lopes-Pires, Mariana R. Brandão-Braga, Raquel J. Campos-e-Nonato, Davi M. Moreira-Antunes

La información completa de afiliaciones y autor de correspondencia está disponible en la versión original en PDF.

*Correspondence: Tânia R.M. de Oliveira-Fernandes. Email: tania.moreno@univasf.edu.br

Abstract

Programmed death-1 inhibitor-induced psoriasis is an uncommon and challenging adverse event, especially when severe and in patients without a dermatological history. We report the case of a 67-year-old man, phototype 2, agronomist, diabetic, receiving pembrolizumab for the treatment of renal cancer, who, after the fifth dose, developed progressive pruritic skin lesions characterized by disseminated erythematous-scaling plaques and papules, with a psoriasis area and severity index of 36. Biopsies revealed chronic psoriasiform dermatitis with eosinophilia, compatible with an immune-mediated reaction. He had previously used moisturizers, oral bilastine, and topical corticosteroids, without improvement. Secukinumab was then introduced in an induction regimen followed by monthly maintenance, with marked improvement after the 2nd monthly dose and sustained response for 6 months. This case highlights the importance of early recognition of cutaneous manifestations associated with immunotherapy and demonstrates that selective interleukin-17A blockade can control induced psoriasis without compromising the continuity of oncologic treatment.

Keywords:  Psoriasis. Immunotherapy. Drug-related side effects and adverse reactions. Immune checkpoint inhibitors. Renal neoplasms. Pembrolizumab.

Contents

The full content will be available shortly. Thank you for your patience!