Abstract
Vemurafenib, a BRAF inhibitor, is FDA-approved for the treatment of metastatic melanoma in patients who harbor the BRAF V600E mutation. By inhibiting BRAF, vemurafenib prevents the mitogen-activated protein kinase (MAPK) pathway from driving melanoma growth. Here we present a patient with paradoxical activation of the MAPK pathway by vemurafenib, ultimately resulting in deleterious cutaneous manifestations. An emphasis on close follow-up is warranted for new or changing lesions for patients on this medication and other BRAF inhibitors.
Original language | English (US) |
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Pages (from-to) | 509-510 |
Number of pages | 2 |
Journal | Journal of drugs in dermatology : JDD |
Volume | 14 |
Issue number | 5 |
State | Published - May 1 2015 |
ASJC Scopus subject areas
- Dermatology