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Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis
Triple-combination therapy with elexacaftor, tezacaftor and ivacaftor has been recently approved for cystic fibrosis patients with at least one F508del mutation in the transmembrane conductance regulator of the cystic fibrosis gene. Among the adverse events of elexacaftor, tezacaftor and ivacaftor,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503821/ https://www.ncbi.nlm.nih.gov/pubmed/36143881 http://dx.doi.org/10.3390/medicina58091204 |
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author | Li Pomi, Federica Di Bartolomeo, Luca Vaccaro, Mario Lentini, Maria Cristadoro, Simona Lucanto, Maria Cristina Lombardo, Mariangela Costa, Stefano Borgia, Francesco |
author_facet | Li Pomi, Federica Di Bartolomeo, Luca Vaccaro, Mario Lentini, Maria Cristadoro, Simona Lucanto, Maria Cristina Lombardo, Mariangela Costa, Stefano Borgia, Francesco |
author_sort | Li Pomi, Federica |
collection | PubMed |
description | Triple-combination therapy with elexacaftor, tezacaftor and ivacaftor has been recently approved for cystic fibrosis patients with at least one F508del mutation in the transmembrane conductance regulator of the cystic fibrosis gene. Among the adverse events of elexacaftor, tezacaftor and ivacaftor, the cutaneous ones have been rarely reported, mainly dealing with urticarial-like rashes. On this topic, we report two cases of Malassezia folliculitis following triple therapy administration in two young females. In the first patient, a papulopustular rush appeared before the folliculitis while in the second patient it was not preceded by other skin manifestations. The diagnosis was confirmed both by dermoscopy and histology. The prompt response to systemic antimycotic drugs provided further evidence for the causative role of Malassezia, requiring no discontinuation of cystic fibrosis therapy. We could hypothesize that the triple regimen treatment may induce changes in the skin microbiome, potentially able to favor colonization and proliferation of Malassezia species. Physicians should be aware of such associations to allow prompt diagnosis and early interventions, avoiding useless drug removal. |
format | Online Article Text |
id | pubmed-9503821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95038212022-09-24 Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis Li Pomi, Federica Di Bartolomeo, Luca Vaccaro, Mario Lentini, Maria Cristadoro, Simona Lucanto, Maria Cristina Lombardo, Mariangela Costa, Stefano Borgia, Francesco Medicina (Kaunas) Case Report Triple-combination therapy with elexacaftor, tezacaftor and ivacaftor has been recently approved for cystic fibrosis patients with at least one F508del mutation in the transmembrane conductance regulator of the cystic fibrosis gene. Among the adverse events of elexacaftor, tezacaftor and ivacaftor, the cutaneous ones have been rarely reported, mainly dealing with urticarial-like rashes. On this topic, we report two cases of Malassezia folliculitis following triple therapy administration in two young females. In the first patient, a papulopustular rush appeared before the folliculitis while in the second patient it was not preceded by other skin manifestations. The diagnosis was confirmed both by dermoscopy and histology. The prompt response to systemic antimycotic drugs provided further evidence for the causative role of Malassezia, requiring no discontinuation of cystic fibrosis therapy. We could hypothesize that the triple regimen treatment may induce changes in the skin microbiome, potentially able to favor colonization and proliferation of Malassezia species. Physicians should be aware of such associations to allow prompt diagnosis and early interventions, avoiding useless drug removal. MDPI 2022-09-02 /pmc/articles/PMC9503821/ /pubmed/36143881 http://dx.doi.org/10.3390/medicina58091204 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Li Pomi, Federica Di Bartolomeo, Luca Vaccaro, Mario Lentini, Maria Cristadoro, Simona Lucanto, Maria Cristina Lombardo, Mariangela Costa, Stefano Borgia, Francesco Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis |
title | Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis |
title_full | Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis |
title_fullStr | Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis |
title_full_unstemmed | Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis |
title_short | Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis |
title_sort | malassezia folliculitis following triple therapy for cystic fibrosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503821/ https://www.ncbi.nlm.nih.gov/pubmed/36143881 http://dx.doi.org/10.3390/medicina58091204 |
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