and sorafenib therapy was restarted without further sequelae. Unlike other cases reported in the literature, the patient described herein and the one described by Bilaç et al 2 had clinically EM-like eruptions with targetoid lesions, nondiagnostic histopathologic findings, and successful reinitiation of sorafenib treatment. Thus, we recommend biopsy of targetoid eruptions during sorafenib therapy to differentiate between a diagnosis of EM and EM-like sorafenib reaction to minimize discontinuation of an antineoplastic agent shown to prolong progression-free survival.