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Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy

Psoriasis is a chronic immune-mediated inflammatory disease. Up to 40% of patients with psoriasis may develop psoriatic arthritis.  Currently, interleukin (IL)-17/IL-23 pathways are identified as key factors in the immunopathogenesis of both conditions. Here we describe the case of a patient who dev...

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Autores principales: Tadiotto Cicogna, Giulia, Messina, Francesco, Nalotto, Linda, Szekely, Serena, Alaibac, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685451/
https://www.ncbi.nlm.nih.gov/pubmed/31448100
http://dx.doi.org/10.12688/f1000research.18493.1
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author Tadiotto Cicogna, Giulia
Messina, Francesco
Nalotto, Linda
Szekely, Serena
Alaibac, Mauro
author_facet Tadiotto Cicogna, Giulia
Messina, Francesco
Nalotto, Linda
Szekely, Serena
Alaibac, Mauro
author_sort Tadiotto Cicogna, Giulia
collection PubMed
description Psoriasis is a chronic immune-mediated inflammatory disease. Up to 40% of patients with psoriasis may develop psoriatic arthritis.  Currently, interleukin (IL)-17/IL-23 pathways are identified as key factors in the immunopathogenesis of both conditions. Here we describe the case of a patient who developed psoriasiform skin lesions 10 months after the initiation of anti-IL17 therapy for psoriatic arthritis. The underlying disease had responded well to the therapy, but the patient developed a striking pustular eruption at the fingers with nail involvement, onycholysis, yellow discoloration, and subungual keratosis. Clinical and histological findings were consistent with an acrodermatitis continua of Hallopeau-like eruption. Skin lesions subsided after discontinuation of the responsible anti-IL17 agent. The interpretation of this paradoxical side effect of biological therapies remains unclear but may relate to an unbalanced inflammatory cytokine response induced by the inhibition of TNF activity. It is likely that patients, who are genetically prone, may respond exaggeratedly to a cytokine imbalance. The identification of this kind of patient, in the future, could be useful in order to choose the correct therapy.
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spelling pubmed-66854512019-08-22 Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy Tadiotto Cicogna, Giulia Messina, Francesco Nalotto, Linda Szekely, Serena Alaibac, Mauro F1000Res Case Report Psoriasis is a chronic immune-mediated inflammatory disease. Up to 40% of patients with psoriasis may develop psoriatic arthritis.  Currently, interleukin (IL)-17/IL-23 pathways are identified as key factors in the immunopathogenesis of both conditions. Here we describe the case of a patient who developed psoriasiform skin lesions 10 months after the initiation of anti-IL17 therapy for psoriatic arthritis. The underlying disease had responded well to the therapy, but the patient developed a striking pustular eruption at the fingers with nail involvement, onycholysis, yellow discoloration, and subungual keratosis. Clinical and histological findings were consistent with an acrodermatitis continua of Hallopeau-like eruption. Skin lesions subsided after discontinuation of the responsible anti-IL17 agent. The interpretation of this paradoxical side effect of biological therapies remains unclear but may relate to an unbalanced inflammatory cytokine response induced by the inhibition of TNF activity. It is likely that patients, who are genetically prone, may respond exaggeratedly to a cytokine imbalance. The identification of this kind of patient, in the future, could be useful in order to choose the correct therapy. F1000 Research Limited 2019-03-26 /pmc/articles/PMC6685451/ /pubmed/31448100 http://dx.doi.org/10.12688/f1000research.18493.1 Text en Copyright: © 2019 Tadiotto Cicogna G et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tadiotto Cicogna, Giulia
Messina, Francesco
Nalotto, Linda
Szekely, Serena
Alaibac, Mauro
Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy
title Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy
title_full Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy
title_fullStr Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy
title_full_unstemmed Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy
title_short Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy
title_sort case report: paradoxical acrodermatitis of hallopeau-like eruption following anti-il-17 therapy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685451/
https://www.ncbi.nlm.nih.gov/pubmed/31448100
http://dx.doi.org/10.12688/f1000research.18493.1
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