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首页> 外文期刊>Melanoma research >Rapidly growing pancreatic ductal adenocarcinoma in a patient with metastatic melanoma and harbouring CDKN2A germline mutation: A new vemurafenib-induced malignancy?
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Rapidly growing pancreatic ductal adenocarcinoma in a patient with metastatic melanoma and harbouring CDKN2A germline mutation: A new vemurafenib-induced malignancy?

机译:患有转移性黑色素瘤且具有CDKN2A种系突变的患者中快速生长的胰腺导管腺癌:新的维罗非尼诱导的恶性肿瘤?

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Selective BRAF inhibitors (vemurafenib) have demonstrated in large controlled trials impressive improvement of the overall and progression-free survivals of patients with BRAFV600-miitated advanced melanoma [1]. Cutaneous squamous cell carcinomas or papillomatous lesions, as well as atypical melanocytic proliferations and new primary melanomas have been, however, reported in vemurafenib-treated patients. A paradoxical activation of the MAPK pathway in cutaneous cells not harboring the BRAFV600 mutation has been postulated [2,3]. These skin cancers and proliferations are easily accessible to early diagnosis and excision, and no death has been reported yet. At present, no vemurafenib-induced internal malignancy has been reported. We report herein a rapidly growing pancreatic ductal adenocarcinoma in a vemurafenib-treated patient.
机译:选择性BRAF抑制剂(vemurafenib)在大型对照试验中已证明,BRAFV600型晚期黑色素瘤患者的总体生存率和无进展生存率得到了显着提高[1]。在维罗非尼治疗的患者中报告了皮肤鳞状细胞癌或乳头状病变,以及非典型的黑素细胞增生和新发的原发性黑色素瘤。假定不具有BRAFV600突变的皮肤细胞中MAPK途径存在反常激活[2,3]。这些皮肤癌和增生很容易进行早期诊断和切除,尚未有死亡报道。目前,尚无维拉非尼引起的内部恶性肿瘤的报道。我们在此报告了在维罗非尼治疗的患者中快速增长的胰腺导管腺癌。

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