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Case of vemurafenib-induced Sweet's syndrome
Jeffrey T Yorio1, Steven R Mays, Ana M Ciurea
1Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Abstract:
Vemurafenib is a targeted therapy that has become standard treatment for patients with advanced melanoma with a V600E BRAF mutation. It has been associated with frequent skin toxicity, including photosensitivity, rash and squamous cell carcinomas. We present an 83-year-old woman with an advanced V600E BRAF-mutant melanoma who developed a severe skin rash and fatigue after taking vemurafenib. The dose was reduced from 960 to 720 to 480 mg twice a day; however, she was subsequently admitted to the hospital with fever, chills, fatigue, confusion and a diffuse skin eruption. She then developed hypoxia and acute renal failure that required hemodialysis. A biopsy of her skin lesions revealed a neutrophilic dermatitis with papillary dermal edema, consistent with Sweet's syndrome. Her symptoms resolved upon discontinuation of vemurafenib and treatment with prednisone. This constellation of symptoms and clinical course are consistent with drug-induced Sweet's syndrome caused by vemurafenib.
Insights
Vemurafenib, a targeted melanoma therapy, can cause severe skin reactions. This case highlights drug-induced Sweet's syndrome, a rare but serious side effect requiring prompt treatment.
Area of Science:
- Dermatology
- Oncology
- Pharmacology
Background:
- Vemurafenib is a standard targeted therapy for advanced melanoma with BRAF V600E mutations.
- Skin toxicities, including rash and photosensitivity, are common adverse effects of vemurafenib treatment.
Observation:
- An 83-year-old woman with advanced BRAF V600E-mutant melanoma developed severe rash and fatigue on vemurafenib.
- Despite dose reduction, she experienced fever, confusion, diffuse skin eruption, hypoxia, and acute renal failure requiring hemodialysis.
Findings:
- Skin biopsy revealed neutrophilic dermatitis with papillary dermal edema, consistent with Sweet's syndrome.
- The patient's symptoms resolved after vemurafenib discontinuation and prednisone treatment.
- This clinical presentation suggests drug-induced Sweet's syndrome secondary to vemurafenib.
Implications:
- Vemurafenib can induce Sweet's syndrome, a rare but serious dermatologic reaction.
- Early recognition and management of vemurafenib-induced Sweet's syndrome are crucial for patient outcomes.
- This case underscores the importance of monitoring for severe cutaneous adverse reactions during targeted melanoma therapy.
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