Abstract

Tyrosine kinase inhibitors (TKI) targeting the bcr-abl protein, c-kit and the platelet-derived growth factor receptors, are significant part of the pathogenic therapy of chronic myelogenous leukemia. A broad spectrum of cutaneous side effects has been described with the clinical use of imatinib mesylate, ranging from various acute rashes to toxic epidermal necrolysis. Herein, a case of cross skin toxicity to TKI in a patient with chronic myelogenous leukemia is presented. In the course of imatinib mesylate therapy the patient developed a grade 4 diffuse lichenoid drug eruption. Six months after switching to nilotinib, hyperpigmented macules and patches spread over his trunk and extremities. To date, few cases of cross skin reactivity to imatinib and nilotinib have been described, none of which showing different clinical phenotypes. Further understanding of the underlying mechanisms and leading to the development of skin rashes from different class of TKI is important to highlight new drug targets and modify the current therapies to a level of maximal efficacy.

Highlights

  • A broad spectrum of cutaneous side effects has been described with the clinical use of imatinib mesylate, ranging from various acute rashes to toxic epidermal necrolysis

  • Imatinib mesylate has revolutionized the treatment of chronic myeloid leukemia (CML) and has been recently approved as first line therapy in CML patients

  • Among skin changes caused by imatinib, the most common adverse effects are superficial skin edema, rashes, hypopigmentation and pruritus [2]. Does it lead to severe epidermal necrolysis, acute generalized exanthematous pustulosis, hyperpigmentation and lichenoid eruption [3,4]

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Summary

Introduction

Imatinib mesylate has revolutionized the treatment of chronic myeloid leukemia (CML) and has been recently approved as first line therapy in CML patients. Frequent non-hematological adverse effects are nausea, musculoskeletal pain, superficial edema, skin rashes and muscular cramps. The prevalence and their relationship with the dose suggest that they are the direct pharmacological effect of imatinib [1]. Among skin changes caused by imatinib, the most common adverse effects are superficial skin edema, rashes, hypopigmentation and pruritus [2]. Does it lead to severe epidermal necrolysis, acute generalized exanthematous pustulosis, hyperpigmentation and lichenoid eruption [3,4]. A case of cross skin intolerance to tyrosine kinase inhibitors in a patient with CML is presented

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