Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1783442402292269056 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6685451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tadiottocicognagiulia casereportparadoxicalacrodermatitisofhallopeaulikeeruptionfollowingantiil17therapy AT messinafrancesco casereportparadoxicalacrodermatitisofhallopeaulikeeruptionfollowingantiil17therapy AT nalottolinda casereportparadoxicalacrodermatitisofhallopeaulikeeruptionfollowingantiil17therapy AT szekelyserena casereportparadoxicalacrodermatitisofhallopeaulikeeruptionfollowingantiil17therapy AT alaibacmauro casereportparadoxicalacrodermatitisofhallopeaulikeeruptionfollowingantiil17therapy |