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Concurrent Eruptive Melanocytic Nevi and Multiple Keratoacanthomas Induced by Encorafenib. | LitMetric

AI Article Synopsis

  • - A case study discusses a 64-year-old male with metastatic colorectal cancer who developed severe itching and new skin lesions after treatment with encorafenib and panitumumab, medications targeting cancer pathways.
  • - The patient showed a mix of skin lesions, including benign moles and keratoacanthomas, with further evaluation confirming a link between the skin reactions and the use of encorafenib, as validated by the Naranjo scale.
  • - Stopping the medications led to significant improvement in skin lesions, highlighting the importance of ongoing skin assessments for patients on BRAF inhibitors to manage side effects effectively.

Article Abstract

Eruptive melanocytic nevi and multiple keratoacanthomas are rare cutaneous conditions, often linked to drug-related toxicities but rarely reported simultaneously, particularly in cancer patients undergoing BRAF-targeted therapies. We present a case of a 64-year-old male with metastatic colorectal cancer who developed severe pruritus and widespread new skin lesions following treatment with encorafenib, a v-Raf murine sarcoma viral oncogene homolog B (BRAF) inhibitor, and panitumumab, an anti-epidermal growth factor receptor (EGFR) monoclonal antibody. The dermatological assessment identified both pigmented and non-pigmented lesions, including benign nevi and keratoacanthomas. Despite close monitoring, larger keratoacanthomas persisted, prompting surgical excision, which confirmed lichenoid keratosis. The Naranjo scale indicated a definite association between encorafenib and cutaneous reactions, with a score of nine. The mitogen-activated protein kinase pathway's role in cutaneous adverse events was explored, suggesting a paradoxical activation mechanism. Discontinuation of encorafenib and panitumumab led to gradual resolution of most lesions, highlighting a possible etiopathogenic link. This study emphasizes the need for thorough dermatologic evaluation and follow-up in patients receiving BRAF inhibitors to optimize management and avoid unnecessary treatment cessation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11524434PMC
http://dx.doi.org/10.7759/cureus.70540DOI Listing

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