A 62-year-old female presented with a palpable mass in her left axilla, which had been present for two months, in September 2014. Contrast-enhanced computed tomography revealed subcutaneous tumors and lymphadenopathy in her left neck, axilla, and scapular region. A needle biopsy of the affected lymph node demonstrated atypical proliferating tumor cells, which were positive for S100 and HMB45. The tumor was too large and had infiltrated too deeply to allow a radical resection to be performed. After the patient had been diagnosed with malignant melanoma, we conducted a mass-reducing operation and combination chemotherapy with dacarbazine and interferon-β. As these were not effective, we started performing chemotherapy with nivolumab. After the administration of two doses of nivolumab, the tumor continued to grow rapidly. As vemurafenib received MHLW (Ministry of Health, Labour and Welfare) approval as a treatment for late-stage melanoma in February 2015, we replaced the nivolumab with vemurafenib. By 4 weeks after the start of vemurafenib therapy, the patient's tumor and lymph node metastases had markedly improved, and her pleural effusion had disappeared. Although the primary and metastatic tumor regrew 3 months later, and the patient died 6 months later, vemurafenib is an effective treatment for aggressive metastatic melanomas carrying BRAF gene mutations.Skin Research, 15: 8-11, 2016
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