Case report demonstrates successful topical management of grade 2 sorafenib-induced hand-foot syndrome in desmoid fibromatosis, highlighting the feasibility of maintaining cancer therapy.
Sorafenib is an oral multikinase inhibitor widely used in the treatment of various solid malignancies and has recently emerged as a therapeutic option for desmoid fibromatosis. Hand-foot syndrome (HFS), also known as palmar-plantar erythrodysesthesia, is a common cutaneous adverse effect associated with sorafenib therapy. Although sorafenib-induced HFS has been well documented in patients with renal cell carcinoma and hepatocellular carcinoma, reports in patients with desmoid fibromatosis (DF) remain limited. We report a case of grade 2 sorafenib-induced HFS in a 21-year-old man receiving sorafenib for DF. Sorafenib continued, and the patient was treated with topical clobetasol propionate 0.05%, salicylic acid 12%, and emollients. Partial clinical improvement was observed after three weeks without dose modification. This case highlights the importance of early recognition and prompt management of sorafenib-induced HFS to ensure treatment adherence and optimize patient outcomes.
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