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The Oncologist, Vol. 12, No. 10, 1178-1182, October 2007; doi:10.1634/theoncologist.12-10-1178
© 2007 AlphaMed Press

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Genitourinary Cancer

Localized Palmar–Plantar Epidermal Hyperplasia: A Previously Undefined Dermatologic Toxicity to Sorafenib

Matthew Beldnera, Michael Jacobsonb, Gene E. Burgesb, Deborah Dewaayc, John C. Maize, Jr.d, Uzair B. Chaudharya

Departments of aHematology/Oncology, bDermatology, and cMedicine, Medical University of South Carolina, Charleston, South Carolina, USA; dDermpath Diagnostics Maize Center for Dermatopathology, Mt. Pleasant, South Carolina, USA

Key Words. Cutaneous manifestations • Tyrosine kinase inhibitors • Dermatologic toxicity • Sorafenib Palmar–plantar erythrodysesthesia • Hand–foot syndrome

Correspondence: Matthew Beldner, M.D., Department of Hematology/Oncology, Medical University of South Carolina, 903 CSB, 96 Jonathan Lucas Street, Charleston, South Carolina 29425, USA. Telephone: 843-792-7834; Fax: 843-792-0644; e-mail: beldner{at}musc.edu

Disclosure: U.B.C. has acted as consultant to Amgen, Genentech, Wyeth, Bristol-Myers Squibb, and Novartis, and has performed contract work for Amgen and Bristol-Myers Squibb within the last 2 years. No other potential conflicts of interest were reported by the authors, planners, reviewers, or staff managers of this article.

The development of multitargeted tyrosine kinase inhibitors has provided significant advances in the treatment of renal cell carcinoma. This case describes initial therapy for managing renal cell cancer with the administration of sorafenib, a multitargeted tyrosine kinase inhibitor. We report the development of localized palmar–plantar epidermal hyperplasia, a rare but significant cutaneous adverse event from sorafenib therapy. Mild-to-moderate dermatologic toxicity from sorafenib has been well described in the literature. We also review the current knowledge and the proposed hypothesis for the development of cutaneous events related to tyrosine kinase inhibitors. This particular case represents a unique form of dermatologic toxicity to sorafenib that has not previously been described in the literature.




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