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Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect

Pembrolizumab is the first anti-programmed death protein-1 agent approved by the US Food and Drug Administration. It has demonstrated efficacy in melanoma, lung cancer, and other advanced solid tumours and hematologic malignancies. Various dermatological side effects including pruritus, maculopapula...

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Autores principales: Bansal, Aditi, Singla, Ankur, Paul, Davinder, Kaur, Sukhjot
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231724/
https://www.ncbi.nlm.nih.gov/pubmed/37266094
http://dx.doi.org/10.4103/idoj.idoj_377_22
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author Bansal, Aditi
Singla, Ankur
Paul, Davinder
Kaur, Sukhjot
author_facet Bansal, Aditi
Singla, Ankur
Paul, Davinder
Kaur, Sukhjot
author_sort Bansal, Aditi
collection PubMed
description Pembrolizumab is the first anti-programmed death protein-1 agent approved by the US Food and Drug Administration. It has demonstrated efficacy in melanoma, lung cancer, and other advanced solid tumours and hematologic malignancies. Various dermatological side effects including pruritus, maculopapular rash, vitiligo, lichenoid skin reactions, psoriasis, and rarely life-threatening conditions like bullous pemphigoid, Stevens-Johnson syndrome, and drug rash with eosinophilia and systemic symptoms have been reported. We report a case of pembrolizumab-induced lichen planus in a 54-year-old female who was receiving pembrolizumab for management of lung metastasis from squamous cell carcinoma of the buccal mucosa. The lichen planus responded to acitretin and pembrolizumab was continued safely.
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spelling pubmed-102317242023-06-01 Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect Bansal, Aditi Singla, Ankur Paul, Davinder Kaur, Sukhjot Indian Dermatol Online J Case Report Pembrolizumab is the first anti-programmed death protein-1 agent approved by the US Food and Drug Administration. It has demonstrated efficacy in melanoma, lung cancer, and other advanced solid tumours and hematologic malignancies. Various dermatological side effects including pruritus, maculopapular rash, vitiligo, lichenoid skin reactions, psoriasis, and rarely life-threatening conditions like bullous pemphigoid, Stevens-Johnson syndrome, and drug rash with eosinophilia and systemic symptoms have been reported. We report a case of pembrolizumab-induced lichen planus in a 54-year-old female who was receiving pembrolizumab for management of lung metastasis from squamous cell carcinoma of the buccal mucosa. The lichen planus responded to acitretin and pembrolizumab was continued safely. Wolters Kluwer - Medknow 2023-04-04 /pmc/articles/PMC10231724/ /pubmed/37266094 http://dx.doi.org/10.4103/idoj.idoj_377_22 Text en Copyright: © 2023 Indian Dermatology Online Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Bansal, Aditi
Singla, Ankur
Paul, Davinder
Kaur, Sukhjot
Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect
title Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect
title_full Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect
title_fullStr Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect
title_full_unstemmed Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect
title_short Pembrolizumab-Induced Lichen Planus: A Rare Immune-Related Adverse Side Effect
title_sort pembrolizumab-induced lichen planus: a rare immune-related adverse side effect
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231724/
https://www.ncbi.nlm.nih.gov/pubmed/37266094
http://dx.doi.org/10.4103/idoj.idoj_377_22
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